Progress: Procedure completed
Role | Committee | Rapporteur | Shadows |
---|---|---|---|
Lead | ENVI | KOPCIŃSKA Joanna ( ECR) | KANEV Radan ( EPP), RÓNAI Sándor ( S&D), ŞTEFĂNUȚĂ Nicolae ( Renew), MÉLIN Joëlle ( ID) |
Committee Opinion | BUDG | HERBST Niclas ( EPP) | Henrike HAHN ( Verts/ALE), Silvia MODIG ( GUE/NGL) |
Lead committee dossier:
Legal Basis:
TFEU 168-p5
Legal Basis:
TFEU 168-p5Subjects
Events
PURPOSE: to extend the mission and tasks of the European Centre for Disease Prevention and Control (ECDC) to strengthen its capacity to provide the necessary scientific expertise and to support actions against serious cross-border health threats in the Union.
LEGISLATIVE ACT: Regulation (EU) 2022/2370 of the European Parliament and of the Council amending Regulation (EC) No 851/2004 establishing a European Centre for Disease Prevention and Control.
CONTENT: this Regulation amending Regulation (EC) No 851/2004 expands the mission and tasks of the European Centre for Disease Prevention and Control (ECDC) in order to strengthen the Centre's capacity to provide the required robust and independent scientific expertise and to support actions relevant to the planning of prevention, preparedness and response to serious cross-border health threats in the Union. The updated mandate of the ECDC is part of the broader package on a European Health Union.
Mission and work of the Centre
To strengthen the capacity of the EU and the Member States to protect human health through the prevention and control of communicable human diseases and related special health issues, the Centre will:
- identify, assess and communicate on current and emerging threats to human health from communicable diseases and related special health issues and, where appropriate, to ensure that information on them is presented in a readily accessible manner. The Centre will act in collaboration with the competent bodies in the Member States or on its own initiative through a dedicated network;
- make science-based recommendations and help coordinate responses to such threats at EU and national level, as well as at inter-regional and regional cross-border level where appropriate. In making such recommendations, the Centre will cooperate, as appropriate, with Member States and take into account existing national crisis management plans and the individual situation of each Member State.
The Centre will respect the responsibilities of the Member States, the Commission and other Union bodies or agencies, and the responsibilities of third countries and international organisations active within the field of public health, in particular the WHO, in order to ensure that there is comprehensiveness, coherence and complementarity of action and that actions are coordinated. It will also support the work of the Health Security Committee (HSC), established by Council Regulation (EU) 2022/2371 on serious transboundary health threats.
Expanded mandate
The Regulation strengthens the mandate of the ECDC so that it can better support the Commission and the Member States, in particular in the following areas:
- providing epidemiological information and analysis, modelling, epidemiological forecasting and anticipation, as well as timely risk assessments and recommendations , based on scientific evidence, which provide options for the prevention and control of communicable diseases;
- monitor, in close cooperation with the Member States, the capacity of Member States' health systems to detect, prevent, respond to and recover from outbreaks of communicable diseases , identify gaps and make science-based recommendations to strengthen health systems;
- develop secure and interoperable digital platforms and applications to support epidemiological surveillance at EU level and provide Member States with scientific and technical advice to set up integrated epidemiological surveillance systems;
- identify emerging health threats and monitor and report on trends in communicable diseases;
- contribute to strengthening the capacity within the EU to diagnose, detect, identify and characterise infectious agents that may threaten public health, by ensuring the operation of a specialised network of EU public health reference laboratories;
- cooperate with Member States to safeguard patients in need of treatment using a substance of human origin from the transmission of such a communicable disease. The Centre should therefore establish and operate a network of services supporting the use of substances of human origin;
- enhance preparedness and response capacity at EU and national level by providing scientific and technical expertise to Member States and the Commission;
- mobilise and deploy outbreak assistance teams, known as the EU Health Task Force , to assist in local responses to disease outbreaks and collect field data;
- inform the general public in an effective and transparent manner about current and emerging health risks.
Obligations of the Member States
Member States will coordinate and cooperate with the Centre in all its missions and tasks by:
- communicating regularly to the Centre data on the surveillance of communicable diseases, related special health issues and other serious cross-border threats to health;
- preventing, responding to and recovering from outbreaks of communicable diseases;
- notifying the Centre of any serious cross-border threats to health, as soon as detected, through the Early Warning and Response System (EWRS);
- identifying, within the scope of the mission of the Centre, competent bodies and public health experts and organisations that could be available to assist in the Union response to serious cross-border threats to health;
- preparing national prevention, preparedness and response plans;
- facilitating the digitalisation of data collection and the data communication process between national and European surveillance systems.
As personal data concerning health are considered sensitive data, any processing of personal data under the Regulation by Member States or the Centre will be subject to the General Data Protection Regulation (GDPR).
ENTRY INTO FORCE: 26.12.2022.
The European Parliament adopted by 542 votes to 43, with 9 abstentions, a legislative resolution on the proposal for a regulation of the European Parliament and of the Council amending Regulation (EC) No 851/2004 establishing a European Centre for Disease Prevention and Control (ECDC).
The European Parliament's position at first reading under the ordinary legislative procedure amends the Commission proposal as follows:
Expanded mandate
The Regulation aims to expand the mission and tasks of the European Centre for Disease Prevention and Control (ECDC) to enhance the Centre’s capacity to provide the required scientific expertise and to support actions which combat serious cross-border threats to health in the Union. The Centre's actions should be consistent with the ‘ One Health ’ approach, recognising the interconnections between human and animal health and the environment, as many outbreaks of communicable diseases are of zoonotic origin.
Mission and work of the Centre
The mission of the Centre will be to:
- identify and assess current and emerging threats to human health from communicable diseases and related special health issues, to report thereon and, where appropriate, to ensure that information thereon is presented in an easily accessible way. The Centre will act in collaboration with competent bodies of the Member States or on its own initiative, through a dedicated network;
- provide science-based recommendations and support in coordinating the response at Union and national levels, as well as at cross-border interregional and regional level, to such threats, where appropriate. In providing such recommendations, the Centre shall, where necessary, cooperate with Member States and take into account existing national crisis management plans and the respective circumstances of each Member State.
The Centre will perform the following tasks:
- search for, collect, collate, evaluate and disseminate relevant scientific and technical data and information, using the most effective technologies, such as, where relevant, artificial intelligence, respecting European standards regarding ethical aspects;
- coordinate standardisation of data collection procedures , and validation, analysis and dissemination of data at Union level;
- monitor, in close cooperation with Member States, their health system capacity and support the collection of data on their health system capacity;
- organise on-site visits in Member States, on a case-by-case basis, in close collaboration with the Member States concerned;
- monitor the capacity of Member States' health systems to detect, prevent, respond to and recover from outbreaks of communicable diseases;
- provide scientific and technical assistance to help Member States develop their detection and sequencing capacities , in particular those Member States that do not have sufficient capacities;
- ensure interoperability of automated applications and other digital tools that support cross-border public health activities;
- mitigate the risks , such as those related to biased datasets, flawed system design, lack of quality data and overdependence on automated decision-making.
The Centre will cooperate with the European Commission, national authorities, EU bodies and international organisations, in particular the WHO, to ensure effective coherence and synergies between their respective activities.
Obligations of Member States
Member States should coordinate and collaborate with the Centre in relation to the mission and tasks set out in the Regulation, by:
- reporting regularly to the Centre, in accordance with agreed timetables, data on the surveillance of communicable diseases (such as HIV, viral hepatitis B and C and tuberculosis), specific related health issues (i.e. antimicrobial resistance and health care associated infections) and other serious transboundary health threats;
- preparing national prevention, preparedness and response plans;
- facilitating the digitalisation of the data collection and the data communication process between national and European surveillance systems to provide the necessary information in a timely manner.
Additional resources
The capacity of the Centre to implement new tasks will depend on the level of financial assistance available from the Union, as well as on the internal and external human resources available. To be able to fulfil the new tasks entrusted to it as a result of the COVID ‑ 19 pandemic, the Centre will need sufficient funding and staffing. Project-oriented funds, such as those allocated under the EU4Health Programme are not sufficient to respond to the Centre’s needs in the future.
The European Parliament adopted by 598 votes to 84, with 13 abstentions, amendments to the proposal for a regulation of the European Parliament and of the Council amending Regulation (EC) No 851/2004 establishing a European Centre for Disease Prevention and Control (ECDC).
The matter was referred back to the committee responsible for interinstitutional negotiations.
The main amendments adopted in plenary concern the following points:
ECDC’s mandate
The regulation should aim to extend the Centre's mission and tasks to strengthen its capacity to provide the necessary scientific expertise and support actions against serious cross-border health threats in the EU to meet the need for a rapid, better coordinated and coherent response to new emerging health threats.
Members want to ensure that the ECDC's mandate is extended beyond communicable diseases to also cover major non-communicable diseases , such as cardiovascular and respiratory diseases, cancer, diabetes and mental illness.
EU Member States should develop national preparedness and response plans and provide timely, comparable and high-quality data so that the Centre can rapidly assess risks, including through epidemiological modelling and forecasting.
Mission and tasks
The Centre’s mission should be to:
- identify, assess, report and, where appropriate, ensure that information is presented in an easily accessible way on current and emerging threats to human health from communicable diseases and relevant major non-communicable diseases and health issues in collaboration with competent bodies of the Member States or on its own initiative, through the dedicated network;
- provide recommendations and support in coordinating the response at Union and national levels, as well as at interregional and regional level, where appropriate. In providing such recommendations, the Centre shall take into account existing national crisis management plans and the respective circumstances of each Member State.
The amending Regulation of the Centre should prioritise pragmatic solutions to improve transparent cooperation and exchange of information, expertise and best practice between Member State authorities and the Commission, the Health Security Committee and the Centre itself, and other EU institutions and agencies, such as the European Medicines Agency (EMA) and the future European Health Emergency Response and Preparedness Authority (HERA). This increased cooperation would allow for better preparedness and coordination of the response plans.
Specifically, the Centre should:
- monitor the capacity of health systems to manage communicable disease threats and other specific health problems on the basis of common indicators;
- organise regular visits to the Member States to assess health systems' capacity to manage health crises and ad hoc inspections to the Member States to verify preparedness and response plans;
- organise case-by-case source inspections in Member States to provide additional support and monitor progress in implementing and complying with the obligations set out in the Regulation, where necessary taking into account the results of stress tests;
- assist in monitoring the national response to the major communicable diseases in order to measure progress in the control of these diseases across the EU;
- inform the general public in an effective and transparent way about current and emerging health risks;
- create a public database of recognised national competent bodies and their public health experts operating within the Centre's remit;
- ensure that its processing operations comply with data protection principles.
In pursuing its mission, the Centre should take full account of the responsibilities and competences of the Member States, the Commission and other Union bodies or agencies, and of the responsibilities of international organisations active within the field of public health, in particular the WHO, to ensure coordination, comprehensiveness, coherence, consistency and complementarity of action.
Additional resources
The capacity of the Centre to implement new tasks will depend on the level of financial assistance available from the Union, as well as on the internal and external human resources available. In order to be able to fulfil the new tasks entrusted to it as a result of the COVID-19 pandemic, the Centre will need increased funding and more employees. Members therefore proposed to increase the Centre’s funding and staffing at the earliest opportunity.
PURPOSE: to reinforce the mandate of the European Centre for Disease Prevention and Control (ECDC) addressing surveillance, preparedness, early warning and response under a strengthened EU health security framework.
PROPOSED ACT: Regulation of the European Parliament and of the Council.
ROLE OF THE EUROPEAN PARLIAMENT: the European Parliament decides in accordance with the ordinary legislative procedure and on an equal footing with the Council.
BACKGROUND: the EU is committed to protect and improve human health, in particular to combat the major cross-border health scourges, measures concerning monitoring, early warning of and combating serious cross-border threats to health.
However, the COVID-19 pandemic has revealed shortcomings in the EU’s mechanisms for managing health threats. The proposal builds on lessons learnt during the COVID-19 crisis, and proposes to strengthen the existing Union level structures and mechanisms for improved levels of protection, prevention, preparedness and response, against all health hazards across the EU.
The proposal is part of a package of closely associated measures that aim to reinforce the crisis preparedness and response and enhance the role of the European Medicines Agency (EMA). Together, they form part of the EU’s overall health response to COVID-19 as well as an improved crisis management framework.
CONTENT: the proposal aims to amend the Centre’s founding regulation in order to reinforce its mandate so that it may support the Commission and Member States in the following areas:
epidemiological surveillance via integrated systems enabling real-time surveillance preparedness and response planning, reporting and auditing situational awareness: rapid digitalisation of integrated surveillance systems; better preparedness in Member States: develop prevention and response plans against future epidemics and stronger capacities for integrated rapid epidemic and outbreak response; reinforced measures to control epidemics and outbreaks: provision of nonbinding recommendations for risk management; reinforced capacity and to identify population groups at risk and in need of targeted prevention and response measures; building up the key competences for health protection in Member States: the Centre will be tasked with coordinating a new network of Union reference laboratories for public health and a new network of national services supporting transfusion, transplantation and medically assisted reproduction; expanding work on the prevention of communicable diseases and specific health issues, e.g., antimicrobial resistance, vaccination and biosecurity; reinforcing the contribution to the EU’s international cooperation and development and EU commitment to global health security preparedness.
Budgetary implications
The financial impact of this proposal on the EU budget should be part of the next Multiannual Financial Framework 2021-2027. The budgetary implications should relate mainly to:
setting-up a new vaccine monitoring platform hosted jointly by the European Medicines Agency and the Centre; new networks on Union reference laboratories and on transfusion, transplantation and medically assisted reproduction; reinforcing surveillance systems and the Early Warning and Response System; monitoring and assessing health systems capacity and identifying population groups at risk and in need of targeted prevention and response measures; creating a ‘EU Health Task Force’ to support countries with preparedness strengthening and quickly intervene in a health crisis; improving international collaboration and gathering of regional/national intelligence.
Documents
- Commission response to text adopted in plenary: SP(2022)623
- Final act published in Official Journal: Regulation 2022/2370
- Final act published in Official Journal: OJ L 314 06.12.2022, p. 0001
- Draft final act: 00082/2021/LEX
- Results of vote in Parliament: Results of vote in Parliament
- Decision by Parliament, 1st reading: T9-0332/2022
- Debate in Parliament: Debate in Parliament
- Decision by Parliament, 1st reading: T9-0376/2021
- Debate in Parliament: Debate in Parliament
- Committee report tabled for plenary, 1st reading/single reading: A9-0253/2021
- Committee report tabled for plenary, 1st reading: A9-0253/2021
- Contribution: COM(2020)0726
- Committee of the Regions: opinion: CDR5624/2020
- Committee opinion: PE663.222
- Amendments tabled in committee: PE691.216
- Contribution: COM(2020)0726
- Committee draft report: PE681.065
- Contribution: COM(2020)0726
- Legislative proposal published: COM(2020)0726
- Legislative proposal published: EUR-Lex
- Committee draft report: PE681.065
- Amendments tabled in committee: PE691.216
- Committee opinion: PE663.222
- Committee of the Regions: opinion: CDR5624/2020
- Committee report tabled for plenary, 1st reading/single reading: A9-0253/2021
- Draft final act: 00082/2021/LEX
- Commission response to text adopted in plenary: SP(2022)623
- Contribution: COM(2020)0726
- Contribution: COM(2020)0726
- Contribution: COM(2020)0726
Votes
Centre européen de prévention et de contrôle des maladies - European Centre for Disease Prevention and Control - Europäisches Zentrum für die Prävention und die Kontrolle von Krankheiten - A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote en bloc - Am 1-8, 10-27, 29-46, 49-88, 91-93, 95-123, 125-152 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 9/1 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 9/2 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 28 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 47/1 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 47/2 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 48 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 89/1 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 89/2 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 90/1 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 90/2 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 94/1 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 94/2 #
A9-0253/2021 - Joanna Kopcińska - Amendements de la commission compétente - vote séparé - Am 124 #
Centre européen de prévention et de contrôle des maladies - European Centre for Disease Prevention and Control - Europäisches Zentrum für die Prävention und die Kontrolle von Krankheiten - A9-0253/2021 - Joanna Kopcińska - Proposition de la Commission #
A9-0253/2021 - Joanna Kopcińska - Renvoi (article 59, paragraphe 4 du règlement) #
Centre européen de prévention et de contrôle des maladies - European Centre for Disease Prevention and Control - Europäisches Zentrum für die Prävention und die Kontrolle von Krankheiten - A9-0253/2021 - Joanna Kopcińska - Accord provisoire - Am 153 #
Amendments | Dossier |
463 |
2020/0320(COD)
2021/03/23
BUDG
34 amendments...
Amendment 10 #
Proposal for a regulation Recital 3 b (new) (3 b) The relationship between the ECDC, EU4Health, the European Medicines Agency and the WHO has to be performant, coherent and seamless and needs to avoid duplication and overlap, both regarding the mandate and the budget.
Amendment 11 #
Proposal for a regulation Recital 4 a (new) (4a) European value added should be constantly established in order to be able to use ECDC diagnoses;
Amendment 12 #
Proposal for a regulation Recital 7 (7) To effectively support the work of the Centre and ensure the fulfilment of its mission, Member States should be tasked, on a voluntary basis and if they deem it necessary, to communicate to the Centre data on the surveillance of communicable diseases and other special health issues such as antimicrobial resistance and healthcare-
Amendment 13 #
Proposal for a regulation Recital 8 a (new) (8 a) One of the lessons of the COVID- 19 pandemic was that the Center needs to be strengthened and that there is a need for more European coordination of disease prevention and control mechanisms. Good coordination at European level of the prevention and control of diseases that are cross-border health threats is essential. To this end, the Center should have the ability to inspect at source how national coordinating bodies apply this Regulation.
Amendment 14 #
Proposal for a regulation Recital 8 a (new) (8 a) These networks should provide the Centre with the necessary data for the swift mitigation of medical supply shortages through joint procurement procedures at Union Level.
Amendment 15 #
Proposal for a regulation Recital 8 b (new) (8 b) The fulfilment of the Centre's tasks and missions depends on an adequate budget and good cooperation and compliance by the Member States. In order to keep track of Member States' progress in implementing the obligations contained in the Regulation, the Centre may carry out source inspections.
Amendment 16 #
Proposal for a regulation Recital 8 b (new) (8 b) To retrieve medical information from data in one or more Member States with a single query a European interconnected database should be foreseen, making data more accessible.
Amendment 17 #
Proposal for a regulation Recital 9 a (new) (9 a) The Centre should analyze the efficiency of its essential systems for detection alerts (EWRS), epidemic intelligence (EPIS) and disease surveillance (TESSy) and make use of new digital technologies available to enhance their capabilities.
Amendment 18 #
Proposal for a regulation Recital 9 b (new) (9 b) The creation of a permanent common European medical emergency units, under the name of EU Blue Medical Corps should be envisaged. This new corps should be composed of medical and emergency intervention professionals from different Member States. Those medical emergency units should be in charge of providing support for cross- border and pan-European medical situations or crisis. The new permanent medical emergency units should use the positive outcomes of the successful voluntary-based medical mobilities financed by the EU Civil Protection Mechanism.
Amendment 19 #
Proposal for a regulation Recital 10 (10) To strengthen the capacity of the Union and Member States to assess the epidemiological situation and perform accurate risk assessment and response, the Centre should in particular monitor and report on trends in communicable diseases, support and facilitate evidence-based response action, provide recommendations for improvement of communicable disease prevention and control programmes established at the national and Union level,
Amendment 20 #
Proposal for a regulation Recital 13 (13) With the aim of reducing the occurrence of epidemics and strengthening capacities to prevent communicable diseases in the Union, the Centre should develop a reasonable framework for the prevention of communicable diseases, which addresses such issues as vaccine preventable diseases, antimicrobial resistance, health education, health literacy and behaviour change.
Amendment 21 #
(14) The Centre should enhance preparedness and response capabilities at national and Union level by providing scientific and technical expertise to the Member States and the Commission. In this context the Centre, in close collaboration with the Member States and the Commission, should carry out various actions, including the development of Union and national preparedness and response plans and preparedness and broader monitoring and evaluation frameworks of the epidemiological situation in Europe, provide recommendations on capacities to prevent, prepare and respond to disease outbreaks and on the strengthening of national health systems. The Centre should broaden its collection and analysis of data in terms of epidemiological surveillance and related special health issues, progression of epidemic situations, unusual epidemic phenomena or new diseases of unknown origin, including in third countries, molecular pathogen data and health systems data. To this end, the Centre should ensure appropriate datasets as well as the procedures to facilitate consultation and data transmission and access, carry out scientific and technical evaluation of prevention and control measures at Union level and work with agencies, competent bodies and organisations operating in the field of data collection.
Amendment 22 #
Proposal for a regulation Recital 16 (16) The Centre should establish appropriate capacities to support international and field response, in accordance with Regulation …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]]. These capacities should enable the Centre to mobilise and deploy outbreak assistance teams, known as ‘EU Health Task Force’, to assist local responses to outbreaks of diseases. The Centre should therefore ensure capacity to carry out missions to Member States that so wish as well as in third countries and to provide recommendations on response to health threats. These teams will also be able to be deployed under the Union Civil Protection Mechanism with the support of the Emergency Response Coordination Centre. The Centre should also support the strengthening of preparedness capacities under the International Health Regulations (IHR) in third countries, in order to address serious cross border threats to health and the consequences thereof.
Amendment 23 #
Proposal for a regulation Recital 22 (22)
Amendment 24 #
Proposal for a regulation Recital 22 (22) Since the objectives of this Regulation to expand the mission and tasks of the Centre in order to enhance the Centre’s capacity to provide the required scientific expertise and to support actions which combat serious cross-border threats to health in the Union cannot be sufficiently achieved by the Member States but can rather, by reason of the cross- border nature of the health threats and the need for rapid, better coordinated and coherent response to new emerging health threats, be achieved at Union level, the Union may adopt measures, in accordance with the principle of subsidiarity as set out in Article 5 of the Treaty on European Union. In accordance with the principle of proportionality as set out in that Article, this Regulation does not go beyond what is necessary in order to achieve those objectives.
Amendment 25 #
Proposal for a regulation Recital 22 a (new) (22 a) The new objectives and responsibilities of the Centre reinforces Union's capacities to support preparedness, surveillance, risk assessment, early warning and rapid response to face future cross-border health threats; they will have a financial impact on the next MFF 2021-27 and therefore should be accompanied by additional resources available under the different flexibility instruments of the annual budgetary procedures; this will ensure that financial capabilities of activities or programmes already foreseen in the domain of public health, such as EU4Health, will not be adversely impacted;
Amendment 26 #
Proposal for a regulation Recital 22 b (new) (22 b) The Centre should promote synergies with other Union bodies and agencies, such as the European Medicines Agency (EMA), the European Food Safety Authority (EFSA), the European Environment Agency (EEA), the European Health Emergency Preparedness and Response Authority (HERA) so to ensure an effective and more coordinated Union preparedness and response in the event health crises;
Amendment 27 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 3 In pursuing its mission, the Centre shall take full account of the responsibilities and competences of the Member States, the Commission and other Union bodies or agencies, and of the responsibilities of international organisations active within the field of public health, in order to ensure comprehensiveness, coherence and complementarity of action, to avoid duplication and to ensure that the principle of subsidiarity is respected.
Amendment 28 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – introductory part 2. The Centre shall, within its
Amendment 29 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point e (e) monitor and inspect health systems’ capacity relevant to the management of communicable disease threats and other special health issues;
Amendment 30 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point j a (new) (j a) provide timely information to the Commission, the Member States, Community agencies and international organisations active within the field of public health;
Amendment 31 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point j b (new) Amendment 32 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 3 3. The Centre, the Commission
Amendment 33 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 3 a (new) 3 a. The Member States shall ensure without delay the coordination and collaboration with the Centre in all the missions and tasks mentioned in article 3.
Amendment 34 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point c a (new) (ca) ensure the financial means and digital infrastructure for the coordinating competent body and facilitate the mission of the Centre by providing timely the information requested
Amendment 35 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point d (d) monitor and
Amendment 36 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 6 a (new) 6 a. The Centre shall provide technical assistance to European laboratories to develop their detection and sequencing capacities especially in Member States that do not have the necessary capacity.
Amendment 37 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 2 2.
Amendment 38 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point i (i) support the competent authorities in the Member States to assess health systems’ capacity to detect, prevent, respond to and recover from outbreaks of communicable diseases, identify gaps and provide recommendations for the strengthening of health systems, to be implemented with Union support as appropriate;
Amendment 39 #
Proposal for a regulation Article 1 – paragraph 1 – point 15 – point a Regulation (EC) No 851/2004 Article 12 – paragraph 1 – subparagraph 2 The Centre shall ensure that the public or any interested party is rapidly given objective, reliable, evidence-based and easily accessible information with regard to the results of its work. The Centre shall make available information for the general public, in
Amendment 6 #
Proposal for a regulation Recital 1 a (new) (1a) Since health continues to be a supporting competence of the EU, Member States should remain in charge of their own health policies;
Amendment 7 #
Proposal for a regulation Recital 2 a (new) (2a) The Commission is called upon to look into the ECDC's tasks and to eliminate overlaps that could result from missions already under way in Member States' agencies;
Amendment 8 #
Proposal for a regulation Recital 3 (3) On 11 March 2020, the World Health Organization (WHO) declared the novel coronavirus COVID-19 outbreak a global pandemic. From the challenges experienced in responding to the pandemic it became clear that the Centre’s role in the Union’s framework for health crisis
Amendment 9 #
Proposal for a regulation Recital 3 a (new) (3 a) European action is targeted to delivering added value, in support and respect of the Member States' competences. Strengthening the existing Union level structures and expertise, ensuring coherence and synergies and avoiding duplication are essential.
source: 663.223
2021/04/07
ENVI
429 amendments...
Amendment 100 #
Proposal for a regulation Recital 8 (8) To enhance preparedness and response planning activities in the Union, the Centre’s operation of dedicated networks and networking activities should be broadened to reflect the scope of Regulation (EU) …/…. [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]]. To this end, the Centre should coordinate and provide technical and scientific expertise to the Commission and Member States through dedicated networks with competent coordinating bodies, including newly established networks for laboratories and for supporting transfusion
Amendment 101 #
Proposal for a regulation Recital 8 (8) To enhance preparedness and response planning activities in the Union, the Centre’s operation of dedicated networks and networking activities should be broadened to reflect the scope of Regulation (EU) …/…. [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]]. To this end, the Centre should coordinate and provide technical and scientific expertise to the Commission and Member States through dedicated networks with competent coordinating bodies, including by encouraging cooperation within newly established networks for laboratories and for supporting transfusion, transplantation and medically assisted reproduction
Amendment 102 #
Proposal for a regulation Recital 8 (8) To enhance preparedness and response planning activities in the Union, the Centre’s operation of dedicated networks and networking activities should be broadened to reflect the scope of Regulation (EU) …/…. [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]]. To this end, the Centre should coordinate and provide technical and scientific expertise to the Commission
Amendment 103 #
Proposal for a regulation Recital 8 (8) To enhance preparedness and response planning activities in the Union, the Centre’s operation of dedicated networks and networking activities should be broadened and strengthened to reflect the scope of Regulation (EU) …/…. [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]]. To this end, the Centre should coordinate and provide technical and scientific expertise to the Commission and Member States through dedicated networks with competent coordinating bodies, including the Union's newly established networks for laboratories and for supporting transfusion, transplantation and medically assisted reproduction,
Amendment 104 #
Proposal for a regulation Recital 8 (8) To enhance preparedness and
Amendment 105 #
Proposal for a regulation Recital 8 a (new) (8a) One of the lessons of the COVID- 19 pandemic was that the Centre needs to be strengthened and that there is a need for more Union coordination of disease prevention and control mechanisms. Good coordination at Union level of the prevention and control of diseases that are cross-border health threats is essential. To this end, the Centre should have the ability to inspect at source how national coordinating bodies apply this Regulation.
Amendment 106 #
Proposal for a regulation Recital 8 b (new) (8b) The fulfilment of the Centre's tasks and missions depends on an adequate budget and good cooperation and compliance by Member States. In order to keep track of Member States' progress in implementing the obligations contained in this Regulation, the Centre should be able to carry out source inspections.
Amendment 107 #
Proposal for a regulation Recital 9 (9) With a view to enhance the effectiveness of epidemiological surveillance
Amendment 108 #
Proposal for a regulation Recital 9 (9) With a view to enhance the effectiveness of epidemiological surveillance of communicable diseases and of the related special health issues in the Union, the Centre should be tasked with the further development of digital platforms and applications, supporting epidemiological surveillance at Union level, enabling the use of digital technologies
Amendment 109 #
Proposal for a regulation Recital 9 (9) With a view to enhance the effectiveness of epidemiological surveillance of communicable diseases and of the related special health issues in the Union, the Centre should be tasked with the further development of digital platforms and applications, supporting epidemiological surveillance at Union level, enabling the use of digital technologies, such as artificial intelligence, in the compilation and analysis of data, and providing Member States with technical and scientific advice to establish integrated epidemiological surveillance systems, with shared objectives and competences that make it possible to progress a European action agenda. Such digital platforms and applications should be developed with integrated EU space generated data with the intention to be integrate them in the future European Health Data Space as governed by the Union legislation.
Amendment 110 #
Proposal for a regulation Recital 9 (9) With a view to enhance the effectiveness of epidemiological surveillance of communicable diseases and of the related special health issues in the Union, the Centre should be tasked with the further development of digital
Amendment 111 #
Proposal for a regulation Recital 9 (9) With a view to enhance the effectiveness of epidemiological surveillance of communicable diseases and of the related special health issues in the Union, the Centre should be tasked with the further development of secure and interoperable digital platforms and applications, supporting epidemiological surveillance at Union level, enabling the use of digital technologies, such as artificial intelligence, in the compilation and analysis of data, and providing Member States with technical and scientific advice to establish integrated epidemiological surveillance systems. Such digital platforms and applications should be developed with integrated EU space generated data with the intention to be integrate them in the future European Health Data Space as governed by the
Amendment 112 #
Proposal for a regulation Recital 9 a (new) (9a) Due to the sensitive nature of the health data, the Centre should safeguard and guarantee its processing operations respect the data protection principles of lawfulness, fairness, transparency, purpose limitation, data minimisation, accuracy, storage limitation, integrity and confidentiality. With respect to the new tasks conferred to the Centre by this Regulation, the Centre should adopt specific measures for minimising risks that can emerge from the transfer of bias or incomplete data from multiple sources, as well as establish procedures for data quality review. The Centre should strictly respect the principles of data protection as set out in Article 27 of Regulation (EU) 2018/17251a, while also determining appropriate technical and organisational security measures in accordance with Article 33 thereof. __________________ 1aRegulation (EU) 2018/1725 of the European Parliament and of the Council of 23 October 2018 on the protection of natural persons with regard to the processing of personal data by the Union institutions, bodies, offices and agencies and on the free movement of such data, and repealing Regulation (EC) No 45/2001 and Decision No 1247/2002/EC (OJ L 295, 21.11.2018, p. 39).
Amendment 113 #
Proposal for a regulation Recital 10 (10) To strengthen the capacity of the Union and Member States to assess the epidemiological situation and perform accurate risk assessment and response, the Centre should in particular monitor and report on trends in communicable diseases, support and facilitate evidence-based response action, provide recommendations for improvement of communicable disease prevention and control programmes established at the national and Union level, monitor and assess the capacity of national health systems for diagnosis, prevention and treatment of communicable diseases, including in a gender-sensitive way, identify population groups at risk requiring specific measures, analyse the correlation of disease incidence with societal and environmental factors, identify possible zoonotic spillovers, and identify risk factors for transmission and disease severity of communicable diseases, and identify research needs and priorities, also in the field of anticipatory research for health, knowing that this type of research puts its focus more on anticipating and preventing future health risks, complementing that research that seeks to solve current health challenges. The Centre should work with nominated national and, where appropriate, regional focal points for surveillance, forming a network that strategically advises the Centre on such matters and would promote the use of enabling sectors, such as EU space data and services.
Amendment 114 #
Proposal for a regulation Recital 10 (10) To strengthen the capacity of the Union and Member States to assess the epidemiological situation and perform accurate risk assessment and response, the Centre should in particular monitor, and report on trends in communicable diseases
Amendment 115 #
Proposal for a regulation Recital 10 (10) To strengthen the capacity of the Union and Member States to assess the epidemiological situation and perform accurate risk assessment and response, the Centre should in particular identify emerging health threats, monitor and report on trends in communicable diseases, support and facilitate evidence-based response action, provide recommendations for improvement of communicable disease prevention and control programmes established at the national and Union level, monitor, inspect and assess the capacity of national health systems for diagnosis, prevention
Amendment 116 #
Proposal for a regulation Recital 10 (10) To strengthen the capacity of the Union and Member States to assess the epidemiological situation and perform accurate risk assessment and response, the Centre should in particular monitor and report on trends in communicable diseases, support and facilitate evidence-based response action, provide recommendations for improvement of communicable disease prevention and control programmes established at the national and Union level, monitor and assess systematically the capacity of national health systems for diagnosis, prevention and treatment of communicable diseases, including in a gender-sensitive way, identify population groups at risk requiring specific measures, analyse the correlation of disease incidence with societal, climate and environmental factors, and identify risk factors for transmission and disease severity of communicable diseases, and identify research needs and priorities. The Centre should work with the European Climate and Health Observatory and with nominated national focal points for surveillance, forming a network that strategically advises the Centre on such matters and would promote the use of enabling sectors, such as EU space data and services.
Amendment 117 #
Proposal for a regulation Recital 10 (10) To strengthen the capacity of the Union and Member States to assess the epidemiological situation and perform accurate risk assessment and response, the Centre should in particular monitor and report on trends in communicable diseases, support and facilitate evidence-based response action, provide recommendations for improvement of communicable disease prevention and control programmes established at the national and Union level, monitor and assess, based on set indicators, the capacity of national health systems for diagnosis, prevention and treatment of communicable diseases, including in a gender-sensitive way, identify population groups at risk requiring specific measures, analyse the correlation of disease incidence with societal and environmental factors, and identify risk factors for transmission and disease severity of communicable diseases, and identify research needs and priorities. The Centre should work with nominated national focal points for surveillance, the WHO and public health experts, forming a network that strategically advises the Centre on such matters and would promote the use of enabling sectors, such as EU space data and services.
Amendment 118 #
Proposal for a regulation Recital 10 (10) To strengthen the capacity of the Union and Member States to assess the epidemiological situation and perform
Amendment 119 #
Proposal for a regulation Recital 10 (10) To strengthen the capacity of the Union and Member States to assess the epidemiological situation and perform accurate risk assessment and response, the Centre should in particular monitor and report on trends in communicable diseases, support and facilitate evidence-based response action, provide recommendations for improvement of communicable disease prevention and control programmes established at the national and Union level,
Amendment 120 #
Proposal for a regulation Recital 10 (10) To strengthen the capacity of the Union and Member States to assess the epidemiological situation and perform timely and accurate risk assessment and response, the Centre should in particular monitor and report on trends in communicable diseases, support and facilitate evidence-based response action, provide recommendations for improvement of communicable disease prevention and control programmes established at the national and Union level, monitor and assess the capacity of national health systems for diagnosis, prevention and treatment of communicable diseases, including in a gender-sensitive way, identify population groups at risk requiring specific measures, analyse the correlation
Amendment 121 #
Proposal for a regulation Recital 11 (11) The Centre should help strengthen the capacity within the Union to diagnose, detect, identify and characterise infectious agents which may threaten public health by ensuring the operation of the network of Union reference laboratories in accordance with Regulation (EU) …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]]. This network is responsible for the promotion of good practice and alignment on diagnostics, testing methods, training in current and innovative procedures and use of tests, in order to ensure uniform surveillance, notification and reporting of diseases, as well as strengthened quality of testing and surveillance.
Amendment 122 #
Proposal for a regulation Recital 11 (11) The Centre should help strengthen the capacity within the Union to diagnose, detect, identify and characterise infectious agents which may threaten public health by ensuring the operation
Amendment 123 #
Proposal for a regulation Recital 11 (11) The Centre should help strengthen the capacity within the Union to anticipate, diagnose, detect, identify and characterise infectious agents which may threaten public health by ensuring the operation of the network of Union reference laboratories in accordance with Regulation (EU) …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]]. This network is responsible for the promotion of good practice and alignment on diagnostics, testing methods, and use of tests, in order
Amendment 124 #
Proposal for a regulation Recital 11 (11) The Centre should help strengthen the capacity within the Union to diagnose, detect, identify and characterise infectious agents which may threaten public health by ensuring the operation of the network of Union reference laboratories in accordance with Regulation (EU) …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]]. Th
Amendment 125 #
Proposal for a regulation Recital 12 (12) Where in case of cross-border health threats posed by communicable
Amendment 126 #
Proposal for a regulation Recital 12 (12) Where in case of cross-border health threats posed by communicable diseases, the blood and transplant services in the Member States can provide a means for rapid testing of the donor population and assessing exposure to and immunity from the disease in the general population. These services are dependent on rapid risk assessments by the Centre to safeguard patients in need of a therapy from a substance of human origin from the transmission of such a communicable disease. Such risk assessments serve as the basis for appropriate adaptation of measures setting standards for quality and safety of the substances of human origin. The Centre should therefore
Amendment 127 #
Proposal for a regulation Recital 12 (12) Where in case of cross-border health threats posed by communicable diseases, the blood and transplant services in the Member States can provide a means for rapid testing of the donor population and assessing exposure to and immunity from the disease in the general population. These services are dependent on rapid and urgent risk assessments by the Centre to safeguard patients in need of a therapy from a substance of human origin from the transmission of such a communicable disease. Such risk assessments serve as the basis for appropriate adaptation of measures setting standards for quality and safety of the substances of human origin. The Centre should therefore establish and operate a network of national blood and transplant services and their authorities to serve this purpose.
Amendment 128 #
Proposal for a regulation Recital 13 (13) With the aim of reducing the occurrence of epidemics and strengthening capacities to prevent communicable diseases in the Union, the Centre should develop a framework for the prevention of communicable diseases
Amendment 129 #
Proposal for a regulation Recital 13 (13) With the aim of reducing the occurrence of epidemics and strengthening capacities to prevent communicable diseases in the Union, the Centre should
Amendment 130 #
Proposal for a regulation Recital 13 (13) With the aim of reducing the occurrence of epidemics and strengthening capacities to prevent communicable diseases in the Union, the Centre should develop a framework for the prevention of communicable diseases, which addresses such issues as
Amendment 131 #
Proposal for a regulation Recital 13 (13) With the aim of reducing the occurrence of epidemics and strengthening capacities to prevent communicable diseases in the Union, the Centre should
Amendment 132 #
Proposal for a regulation Recital 13 (13) With the aim of reducing the occurrence of epidemics and strengthening capacities to prevent communicable diseases in the Union, the Centre should, working in conjunction with Member States so as to take account of their experiences and respective situations, develop a framework for the prevention of communicable diseases, which addresses such issues as vaccine preventable diseases, awareness of transmission routes, antimicrobial resistance, health education,
Amendment 133 #
Proposal for a regulation Recital 13 (13) With the aim of reducing the occurrence of epidemics and strengthening capacities to prevent communicable diseases in the Union, the Centre should develop a framework for the prevention of communicable diseases,
Amendment 134 #
Proposal for a regulation Recital 13 (13) With the aim of reducing the occurrence of epidemics and strengthening
Amendment 135 #
Proposal for a regulation Recital 13 (13) With the aim of reducing the occurrence of epidemics and strengthening capacities to prevent communicable diseases in the Union, the Centre should develop a framework for the prevention of communicable diseases, which addresses such issues as vaccine preventable diseases, antimicrobial resistance, health education, health literacy and behaviour change. The Centre should provide guidelines and monitor the implementation of the framework by Member States.
Amendment 136 #
Proposal for a regulation Recital 13 (13) With the aim of reducing the occurrence of epidemics and strengthening capacities to prevent communicable diseases in the Union, the Centre should develop a framework for the prevention of communicable diseases, which addresses such issues as vaccine preventable diseases, antimicrobial resistance, health education, health literacy and behaviour change. This framework should be aligned with the best evidence available and WHO guidelines, when available.
Amendment 137 #
Proposal for a regulation Recital 13 (13) With the aim of reducing the occurrence of epidemics and strengthening resilience and capacities to prevent communicable diseases in the Union, the Centre should develop a framework for the prevention of communicable diseases, which addresses such issues as vaccine preventable diseases, antimicrobial resistance, health education, health literacy and behaviour change.
Amendment 138 #
Proposal for a regulation Recital 14 (14) The Centre should enhance preparedness and response capabilities at national and Union level by providing scientific and technical expertise to the Member States and the Commission. In this context the Centre, in close collaboration with the Member States and the Commission, should carry out various actions, including the development of Union
Amendment 139 #
Proposal for a regulation Recital 14 (14) The Centre should enhance preparedness and response capabilities at national and Union level by providing scientific and technical expertise to the Member States and the Commission. In this context the Centre, in close collaboration with the Member States and the Commission, should carry out various actions, including the development and coordination of Union and national preparedness and response plans and preparedness monitoring and evaluation frameworks, provide recommendations on capacities to prevent, prepare and respond to disease outbreaks and on the strengthening of national health systems. The Centre should broaden its collection and analysis of data in terms of epidemiological surveillance and related special health issues, progression of epidemic situations, unusual epidemic phenomena or new diseases of unknown origin, including in third countries, data on interconnections between communicable diseases and chronic conditions and especially on major as well as infection- based chronic diseases, molecular pathogen data and health systems data. To this end, the Centre should ensure appropriate datasets as well as the procedures to facilitate consultation and data transmission and access, carry out scientific and technical evaluation of prevention and control measures at Union level and work with agencies, competent bodies and organisations operating in the field of data collection.
Amendment 140 #
Proposal for a regulation Recital 14 (14) The Centre should enhance preparedness and response capabilities at national and Union level by providing scientific and technical expertise to the Member States and the Commission. In this context the Centre, in close collaboration with the Member States and the Commission, should carry out various actions, including the development of Union and national preparedness and response plans and preparedness monitoring and evaluation frameworks, provide recommendations on capacities to prevent, prepare and respond to disease outbreaks and on the strengthening of national health systems. The Centre should broaden its collection and analysis of data in terms of epidemiological surveillance and related special health issues, progression of epidemic situations, unusual epidemic phenomena or new diseases of unknown origin, including in third countries, molecular pathogen data and health systems data. To this end, the Centre should ensure appropriate datasets, complying with the rules laid down by the General Data Protection Regulation and the national rules in force, as well as the procedures to facilitate consultation and data transmission and access, carry out scientific and technical evaluation of prevention and control measures at Union level and work with agencies, competent bodies and organisations operating in the field of data collection.
Amendment 141 #
Proposal for a regulation Recital 14 (14) The Centre should enhance preparedness and response capabilities at regional, national and Union level by providing scientific and technical expertise to the Member States and the Commission. In this context the Centre, in close collaboration with the Member States, regional centres where appropriate, and the Commission, should carry out various actions, including the development of Union and national preparedness and response plans and preparedness monitoring and evaluation frameworks, provide recommendations on capacities to prevent, prepare and respond to disease outbreaks and on the strengthening of national health systems. The Centre should broaden its collection and analysis of data in terms of epidemiological surveillance and related special health issues, progression of epidemic situations, unusual epidemic phenomena, zoonotic disruptions and spillovers, or new diseases of unknown origin, including in third countries, molecular pathogen data and health systems data. To this end, the Centre should ensure appropriate datasets as well as the procedures to facilitate consultation and data transmission and access, carry out scientific and technical evaluation of prevention and control measures at Union level and work with agencies, competent bodies and organisations operating in the field of data collection both in the Union and abroad.
Amendment 142 #
Proposal for a regulation Recital 14 (14) The Centre should enhance preparedness and response capabilities at national and Union level by providing independent scientific and technical expertise to the Member States and the Commission. In this context the Centre, in close collaboration with the Member States and the Commission, should carry out various actions, including the development of Union and national preparedness and response plans and preparedness monitoring and evaluation frameworks, provide recommendations on capacities to prevent, prepare and respond to disease outbreaks and on the strengthening of national health systems. The Centre should ensure the One Health approach and broaden its collection and analysis of data in terms of epidemiological surveillance and related special health and environment issues, progression of epidemic situations, unusual epidemic phenomena or new diseases of unknown origin, including in third countries, molecular pathogen data and health systems data. To this end, the Centre should ensure appropriate datasets as well as the procedures to facilitate consultation and data transmission and access, carry out scientific and technical evaluation of prevention and control measures at Union level and work with the WHO, Union and national agencies, competent bodies and other organisations operating in the field of data collection.
Amendment 143 #
Proposal for a regulation Recital 14 (14) The Centre should enhance preparedness and response capabilities at national and Union level by providing scientific and technical expertise to the Member States and the Commission. In this context the Centre, in close collaboration with the Member States and the Commission, should carry out various actions, including the development of Union and national preparedness and response plans and preparedness monitoring and evaluation frameworks, provide recommendations on capacities to prevent, prepare and respond to disease outbreaks and on the strengthening of national health systems, including by providing training and sharing of best practices. The Centre should broaden its collection and analysis of data in terms of epidemiological surveillance and related special health issues, progression of epidemic situations, unusual epidemic phenomena or new diseases of unknown origin, including in third countries, molecular pathogen data and health systems data. To this end, the Centre should ensure appropriate datasets as well as the procedures to facilitate consultation and secure data transmission and access, carry out scientific and technical evaluation of prevention and control measures at Union level and work with agencies, competent bodies and organisations operating in the field of data collection.
Amendment 144 #
Proposal for a regulation Recital 14 (14) The Centre should enhance preparedness and response capabilities at national and Union level by providing scientific and technical expertise to the Member States and the Commission. In this context the Centre, in close collaboration with the Member States and the Commission, should carry out various actions, including the development of Union
Amendment 145 #
Proposal for a regulation Recital 14 (14) The Centre should enhance preparedness and response capabilities at national and Union level by providing scientific and technical expertise to the Member States and the Commission. In this context the Centre, in close collaboration with the Member States and the Commission, should carry out various actions, including the development of multi-sectoral Union and national preparedness and response plans and preparedness monitoring and evaluation frameworks, provide recommendations on capacities to prevent, prepare and respond to disease outbreaks and on the strengthening of national health systems. The Centre should broaden its collection and analysis of data in terms of epidemiological surveillance and related special health issues, progression of epidemic situations, unusual epidemic phenomena or new diseases of unknown origin, including in third countries, molecular pathogen data and health systems data. To this end, the Centre should ensure appropriate datasets as well as the procedures to facilitate consultation and data transmission and access, carry out scientific and technical evaluation of prevention and control measures at Union level and work with agencies, competent bodies and organisations operating in the field of data collection.
Amendment 146 #
Proposal for a regulation Recital 14 (14) The Centre should enhance preparedness and response capabilities at national and Union level by providing scientific and technical expertise to the Member States and the Commission. In this context the Centre, in close collaboration with the Member States and the Commission, should carry out various actions, including the development of Union and national preparedness and response plans and preparedness monitoring and evaluation frameworks, provide recommendations
Amendment 147 #
Proposal for a regulation Recital 14 a (new) (14a) The Centre should broaden its collection and analysis of data in terms of epidemiological surveillance and related special health issues, non-communicable diseases, vaccine effectiveness and long- term immunity, progression of epidemic situations, unusual epidemic phenomena or new diseases of unknown origin, including in third countries, molecular pathogen data and health systems data. To this end, the Centre should ensure appropriate datasets as well as the procedures to facilitate consultation and data transmission and access, carry out scientific and technical evaluation of prevention and control measures at Union level and work with agencies, competent bodies and organisations operating in the field of data collection.
Amendment 148 #
Proposal for a regulation Recital 15 (15) Regulation …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]] provides for the early warning and response system enabling the notification at Union level of alerts related to serious cross-border threats to health which continues to be operated by the ECDC.
Amendment 149 #
Proposal for a regulation Recital 15 (15) Regulation …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]] provides for the early warning and response system enabling the notification at Union level of alerts related to serious cross-border threats to health which continues to be operated by the ECDC. Given that modern technologies can be of substantial support to combat health threats and to contain and reverse epidemics, the ECDC should work on updating this system to enable the use of artificial intelligence technologies and interoperable and privacy-preserving digital tools, such as mobile applications, with tracing functionalities identifying at- risk individuals, noting in particular references to the risks posed by Artificial Intelligence (AI), for example biased datasets, flawed system design, lack of quality data, overdependence on automated decision-making etc., and the importance of establishing safeguards to mitigate these risks during the design and implementation phases of AI technologies.
Amendment 150 #
Proposal for a regulation Recital 15 (15) Regulation .../... [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]] provides for the early warning and response system enabling the notification at Union level of alerts related to serious cross-border threats to health which continues to be operated by the ECDC. Given that modern technologies can be of substantial support to combat health threats and to contain and reverse epidemics, the ECDC should work on updating this system to enable the use of artificial intelligence technologies and interoperable and privacy-preserving digital tools, such as mobile applications, with tracing functionalities identifying at- risk individuals while complying with the principle of proportionality and fully respecting the fundamental rights of citizens.
Amendment 151 #
Proposal for a regulation Recital 15 (15) Regulation …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]] provides for the early warning and response system enabling the notification at Union level of alerts related to serious cross-border threats to health which continues to be operated by the ECDC. Given that modern technologies can be of substantial support to combat health threats and to contain and reverse
Amendment 152 #
Proposal for a regulation Recital 15 (15) Regulation …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]] provides for the early warning and response system enabling the notification at Union level of alerts related to serious cross-border threats to health which continues to be operated by the ECDC. Given that modern technologies can be of substantial support to combat health threats and to contain and reverse epidemics, the ECDC should work on updating this system to enable the use of artificial intelligence, High Performance Computing, in silico clinical trials and digital twin technologies and interoperable and privacy-preserving digital tools, such as mobile applications, with tracing functionalities identifying at-
Amendment 153 #
Proposal for a regulation Recital 15 (15) Regulation …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]] provides for the early warning and response system enabling the notification at Union level of alerts related to serious cross-border threats to health which continues to be operated by the ECDC. Given that modern technologies can be of substantial support to combat health threats and to contain and reverse epidemics, the ECDC should work on updating this system to enable the use of artificial intelligence technologies and interoperable and privacy-preserving digital tools, such as distributed ledger technology, or mobile applications, with tracing functionalities identifying at-
Amendment 154 #
Proposal for a regulation Recital 16 (16) The Centre should establish appropriate capacities to support international and field response, in accordance with Regulation …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]]. These capacities should enable the Centre to mobilise and deploy outbreak assistance teams, known as ‘EU Health Task Force’, to assist local responses to outbreaks of diseases. The Centre should therefore ensure capacity to carry out missions to Member States as well as in third countries
Amendment 155 #
Proposal for a regulation Recital 16 (16) The Centre should establish appropriate capacities to support international and field response, in accordance with Regulation …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]]. These capacities should enable the Centre to mobilise and deploy outbreak assistance teams, known as ‘EU Health Task Force’, to assist local responses to outbreaks of diseases. The Centre should therefore ensure capacity to carry out missions to Member States as well as in third countries and to provide recommendations on response to health threats. These recommendations should be highly regarded in all Member States in case an outbreak is considered by the Centre to be a high threat. These teams will also be able to be deployed under the Union Civil Protection Mechanism with the support of the Emergency Response Coordination Centre. The Centre should also support the strengthening of
Amendment 156 #
Proposal for a regulation Recital 16 (16) The Centre should establish appropriate capacities to support international and field response, in accordance with Regulation …/… [OJ: Please, insert reference to Regulation SCBTH [ISC/2020/12524]]. These capacities should enable the Centre to mobilise and deploy outbreak assistance teams, known as ‘EU Health Task Force’, to assist local responses to outbreaks of diseases. The Centre should therefore ensure capacity to carry out missions to Member States, at their request, as well as in third countries and to provide recommendations on response to health threats. These teams will also be able to be deployed under the Union Civil Protection Mechanism with the support of the Emergency Response Coordination Centre. The Centre should also support the strengthening of preparedness capacities under the International Health Regulations (IHR) in third countries, in order to address serious cross border threats to health and the consequences thereof.
Amendment 157 #
Proposal for a regulation Recital 16 (16) The Centre should establish appropriate capacities to support international, interregional and field response, in accordance with Regulation …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]]. These capacities should enable the Centre to mobilise and deploy outbreak assistance teams, known as ‘EU Health Task Force’, to assist local responses to outbreaks of diseases. The Centre should therefore ensure permanent capacity to carry out missions to Member States as well as in third countries and to provide recommendations on response to health threats. These teams will also be able to be deployed under the Union Civil Protection Mechanism with the support of the Emergency Response Coordination Centre. The Centre should also support the strengthening of preparedness capacities under the International Health Regulations (IHR) in third countries, in order to address serious cross border threats to health and the consequences thereof.
Amendment 158 #
Proposal for a regulation Recital 16 (16) The Centre should establish appropriate capacities to support international and field response, in accordance with Regulation …/… [OJ: please, insert reference to Regulation SCBTH [ISC/2020/12524]]. These capacities should enable the Centre to mobilise and deploy outbreak assistance teams, known as ‘EU Health Task Force’, to assist local responses to outbreaks of diseases and collect field data. The Centre should therefore ensure capacity to carry out missions to Member States as well as in third countries and to provide recommendations on response to health threats. These teams will also be able to be deployed under the Union Civil Protection Mechanism with the support of the Emergency Response Coordination Centre. The Centre should also support the strengthening of preparedness capacities under the International Health Regulations (IHR) in third countries, in order to address serious cross border threats to health and the consequences thereof.
Amendment 159 #
Proposal for a regulation Recital 17 (17) To assist responses to outbreaks, which may spread within or to the Union, the Centre is to develop a permanent EU Health Task Force and a framework for
Amendment 160 #
Proposal for a regulation Recital 17 (17) To assist responses to outbreaks, which may spread within or to the Union, the Centre is to develop a framework for the mobilisation the EU Health Task Force in accordance with Decision No 1313/2013/EU of the European Parliament and of the Council11 and facilitate the
Amendment 161 #
Proposal for a regulation Recital 17 a (new) Amendment 162 #
Proposal for a regulation Recital 17 b (new) (17b) The Centre should work in close cooperation with the competent bodies and the international organisations in the field of public health in particular the World Health Organization (WHO).
Amendment 163 #
Proposal for a regulation Recital 17 c (new) (17c) The Centre should communicate in an effective and transparent manner about current and emerging health risks to the general public. The Centre should timely publish the scientific studies, overviews, surveys, reports, rapid risk assessments and the assessments of the health systems’ capacities in order to increase transparency. The Centre should in this regard address issues regarding transparency as stated in the European Ombudsman’s decision in strategic inquiry OI/3/2020/TE.
Amendment 164 #
Proposal for a regulation Recital 17 d (new) (17d) The Centre should ensure gender and geographical balance at staff and management levels as well as ensure a gender sensitive approach in all its operations.
Amendment 165 #
Proposal for a regulation Recital 18 (18) In order to assess the effectiveness and efficiency of the legal provisions applicable to the Centre, it is appropriate to provide for a
Amendment 166 #
Proposal for a regulation Recital 19 (19) This Regulation should not confer any regulatory powers on the Centre. However, the Centre should exercise broad coordination competences and the power to provide recommendations at Union, national and interregional level in the form of clear and uniform science- based proposals.
Amendment 167 #
Proposal for a regulation Recital 19 (19) This Regulation should not confer any regulatory powers on the Centre. For this purpose, the Centre should take all technological means necessary to strengthen its cybersecurity processes and hardware.
Amendment 168 #
Proposal for a regulation Recital 20 a (new) (20a) Where processing of personal data is not necessary to perform the activities of the Centre, measures should be put in place to ensure use of anonymous data in line with the principle of data minimisation. Where anonymisation would not allow to achieve the specific purpose of the processing, the data should be pseudonymised. Where it is necessary for the purposes of this Regulation to process personal data, this should be done in accordance with Union law on the protection of personal data. Any processing of personal data based on this Regulation should take place in accordance with Regulations (EU) 2016/679 and Regulation (EU) 2018/1725.
Amendment 169 #
Proposal for a regulation Recital 20 a (new) Amendment 170 #
Proposal for a regulation Recital 20 a (new) (20a) Where processing of personal data is not necessary to perform the activities of the Centre, use of anonymous data and otherwise pseudonymous data should be ensured, in line with the principle of data minimisation. The anonymisation should consist of rendering personal data anonymous in such a manner that the data subject is not or no longer identifiable, through techniques such as the randomisation (altering the veracity of the data in order to remove the strong link between the data and the individual) or generalisation (consisting of generalising or diluting, the attributes of data subjects by modifying the respective scale or order of magnitude).
Amendment 171 #
Proposal for a regulation Recital 20 a (new) (20a) Where it is necessary for the purposes of this Regulation to process personal data, this should be done in accordance with the Union law on the protection of personal data. Any processing of personal data based on this Regulation should take place in accordance with Regulations (EU) 2016/6791a and (EU) 2018/17251b and with Directive 2002/58/EC1c. __________________ 1aRegulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 2016 on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and repealing Directive 95/46/EC (General Data Protection Regulation) (OJ L 119, 4.5.2016, p. 1). 1bRegulation (EU) 2018/1725 of the European Parliament and of the Council of 23 October 2018 on the protection of natural persons with regard to the processing of personal data by the Union institutions, bodies, offices and agencies and on the free movement of such data, and repealing Regulation (EC) No 45/2001 and Decision No 1247/2002/EC (OJ L 295, 21.11.2018, p. 39). 1cDirective 2002/58/EC of the European Parliament and of the Council of 12 July 2002 concerning the processing of personal data and the protection of privacy in the electronic communications sector (Directive on privacy and electronic communications) (OJ L 201, 31.7.2002, p. 37).
Amendment 172 #
Proposal for a regulation Recital 20 a (new) Amendment 173 #
Proposal for a regulation Recital 20 b (new) Amendment 174 #
Proposal for a regulation Recital 22 (22) Since the objectives of this Regulation to expand the mission and tasks of the Centre in order to enhance the Centre’s capacity to provide the
Amendment 175 #
Proposal for a regulation Article 1 – paragraph 1 – point 1 Regulation (EC) No 851/2004 Article 2 – paragraph 1 – point 1 (1) ‘competent body’ means any structure, institute, agent or other scientific body recognised by Member States
Amendment 176 #
Proposal for a regulation Article 1 – paragraph 1 – point 1 Regulation (EC) No 851/2004 Article 2 – paragraph 1 – point 1 a ( new ) (1a) ‘prevention and control of human disease’ means the range of recommendations issued and measures taken by the competent public health authorities in the Member States and the Union, such as the Centre, to prevent, contain and mitigate the spread of disease;
Amendment 177 #
Proposal for a regulation Article 1 – paragraph 1 – point 1 Regulation (EC) No 851/2004 Article 2 – paragraph 1 – point 3 (3) ‘dedicated network’ means any specific network on diseases, special health issues or public health functions, set up, coordinated or supported by the Centre to ensure collaboration between the coordinating competent bodies of the Member States;
Amendment 178 #
Proposal for a regulation Article 1 – paragraph 1 – point 1 Regulation (EC) No 851/2004 Article 2 – paragraph 1 – point 4 a (new) (4a) ‘major non-communicable disease’ means a chronic disease which tends to be of long duration and is the result of a combination of genetic, physiological, environmental and behavioural factors, such as a cardiovascular disease, cancer, respiratory disease, diabetes or mental illness, and which affects a significant number of people in the Union;
Amendment 179 #
Proposal for a regulation Article 1 – paragraph 1 – point 1 Regulation (EC) No 851/2004 Article 2 – paragraph 1 – point 6 a (new) (6a) ‘other special health issues’ means any effect on physical or mental health associated with communicable diseases or with any other crossborder threat to health;
Amendment 180 #
Proposal for a regulation Article 1 – paragraph 1 – point 1 Regulation (EC) No 851/2004 Article 2 – paragraph 1 – point 6 a (new) (6a) ‘non-communicable disease’ means a non-communicable disease as defined by the World Health Organisation;
Amendment 181 #
Proposal for a regulation Article 1 – paragraph 1 – point 1 Regulation ( EC) No 851/2004 Article 2 – paragraph 1 – point 6 a (new) (6a) ‘Health in All Policies’ means Health in All Policies as defined in point (10) of Article 2 of Regulation (EU)2021/522 of the European Parliament and of the Council (‘EU4Health Programme’); __________________ 1a Regulation (EU) 2021/522 of the European Parliament and of the Council of 24 March 2021 establishing a Programme for the Union’s action in the field of health (‘EU4Health Programme’) for the period 2021-2027, and repealing Regulation (EU) No 282/2014 (OJ L 107, 26.3.2021, p. 1).
Amendment 182 #
Proposal for a regulation Article 1 – paragraph 1 – point 1 Regulation ( EC) No 851/2004 Article 2 – paragraph 1 – point 6 b (new) (6b) ‘One Health approach’ means a One Health approach as defined in point (5) of Article 2 of Regulation (EU) 2021/522;
Amendment 183 #
Proposal for a regulation Article 1 – paragraph 1 – point 1 Regulation ( EC) No 851/2004 Article 2 – paragraph 1 – point 6 c ( new ) (6c) ‘zoonosis’ means an infectious disease that has jumped from a non- human animal to humans through zoonotic spillover;
Amendment 184 #
Proposal for a regulation Article 1 – paragraph 1 – point 1 Regulation ( EC) No 851/2004 Article 2 – paragraph 1 – point 6 d ( new ) (6d) ‘zoonotic spillover’ means the spread of a non-human disease to humans resulting in zoonosis;
Amendment 185 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 1 In order to enhance the capacity of the Union and the Member States to protect human health through the prevention and control of communicable diseases in
Amendment 186 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 1 In order to enhance the capacity of the Union and the Member States to protect human health through the prevention and control of communicable diseases in humans and those related special health issues set out in Article 2 of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]],
Amendment 187 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 1 In order to enhance the capacity of the Union and the Member States to protect human health through the prevention and control of communicable diseases in humans and related diseases and health issues, including th
Amendment 188 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 1 In order to enhance the capacity of the Union and the Member States to protect human health through the prevention and control of communicable diseases in humans and those related special health issues set out in Article 2 of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]], the mission of the Centre shall be to identify, assess and report on current and emerging threats to human health from communicable diseases, and provide recommendations for response at Union and national levels, as well as at regional level,
Amendment 189 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 1 In order to enhance the capacity of the Union and the Member States to protect human health through the prevention and control of communicable diseases in humans and those related special health issues set out in Article 2 of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]], the mission of the Centre shall be to identify, assess and report on current and emerging threats to human health from communicable diseases and other cross- border threats to health, and provide recommendations for response at Union and national levels, as well as at regional level, if necessary.
Amendment 190 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 1 In order to enhance the capacity of the Union and the Member States to protect human health through the prevention and control of communicable diseases in humans and those related special health issues set out in Article 2 of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]], the mission of the Centre shall be to identify, assess and report on current and emerging threats to human health from communicable diseases and non- communicable diseases, and provide recommendations for response at Union and national levels, as well as at regional
Amendment 191 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 1 In order to enhance the capacity of the Union and the Member States to protect human health, in the context of the One Health approach, through the prevention and control of communicable diseases in humans and those related special health issues set out in Article 2 of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]], the mission of the Centre shall be to identify, assess and report on current and emerging threats to human health from communicable diseases, and provide recommendations for response at Union and national levels, as well as at regional level, if necessary.
Amendment 192 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 1 In order to enhance the capacity of the Union and the Member States to protect
Amendment 193 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 1 In order to enhance the capacity of the Union and the Member States to protect human health through the prevention and control of communicable diseases in humans and those related special health issues set out in Article 2 of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]], the mission of the Centre shall be to identify, assess and report on current and emerging threats to human health from communicable diseases, and provide recommendations for response at Union and national levels, as well as at regional and local level, if necessary.
Amendment 194 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 2 In the case of other outbreaks of illnesses of unknown origin, such as zoonotic spillovers, that may spread within or to the Union, the Centre shall act on its own initiative until the source of the outbreak is known. In the case of an outbreak that clearly is not caused by a communicable disease, the Centre shall act only in cooperation with the competent body upon request from that body.
Amendment 195 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 2 In the case of other outbreaks of illnesses of unknown origin that may spread within or to the Union, the Centre shall act on its own initiative until the source of the outbreak is known. In the case of an outbreak that clearly is not caused by a communicable disease, the Centre shall act
Amendment 196 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 2 In the case of other outbreaks of illnesses of unknown origin that may spread within or to the Union, the Centre shall act on its own initiative until the source of the outbreak is known. In the case of an outbreak that clearly is not
Amendment 197 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 2 In the case of other outbreaks of illnesses of unknown origin that may spread within or to the Union, the Centre shall act on its own initiative until the source of the outbreak is known. In the case of an outbreak that clearly is not caused by a communicable disease, the Centre shall act only in cooperation with the competent national body upon request from that body.
Amendment 198 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 3 In pursuing its mission, the Centre shall take full account of the responsibilities of the Member States, the Commission and other Union bodies or agencies, and of the responsibilities of international organisations active within the field of public health, in order to ensure comprehensiveness, coherence and complementarity of action. Special cooperation shall be foreseen with the European Medicines Agency, the European Environmental Agency and the Commission.
Amendment 199 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 3 In pursuing its mission, the Centre shall take full account of the responsibilities of the Member States, the Commission and other Union bodies or agencies, and of the responsibilities of international organisations active within the field of public health, in order to ensure coordination, comprehensiveness, coherence, consistency and
Amendment 200 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 1 – subparagraph 3 In pursuing its mission, the Centre shall take full account of the requests and responsibilities of the Member States, the Commission and other Union bodies or agencies, and of the requests and responsibilities of international organisations active within the field of public health, in order to ensure comprehensiveness, coherence and complementarity of action.
Amendment 201 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – introductory part The Centre shall, within its
Amendment 202 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point a (a) search for, collect, collate, evaluate and disseminate relevant scientific and technical data and information, considering the latest technologies, and if necessary in anticipation of the spread of an epidemic;
Amendment 203 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point a (a) search for, collect, collate, evaluate and disseminate relevant scientific and technical data and information,
Amendment 204 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point a a (new) (aa) develop relevant indicators to be used by Member States for assessing the management of communicable diseases;
Amendment 205 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point a a (new) (aa) develop specific indicators for risk assessment and standardised data collection procedures;
Amendment 206 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point b (b) provide analyses, scientific advice, opinions and support for actions by the Union and Member States on cross-border health threats, including risk assessments, analysis of epidemiological information, epidemiological modelling, anticipation and forecast, recommendations for actions to prevent and control communicable disease threats and other special health
Amendment 207 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point b (b) provide analyses, scientific advice, opinions and support for actions by the Union and Member States on cross-border health threats, including risk assessments, analysis of epidemiological information, epidemiological modelling, anticipation and forecast, recommendations for actions to prevent and control communicable disease threats and other special health issues, assessment of the impact of communicable diseases on healthcare systems and care delivery, contribution to defining research priorities, and scientific and technical assistance including training and other activities within its mandate;
Amendment 208 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point b (b) provide analyses, scientific advice, opinions, guidelines and support for actions by the Union and Member States on cross-border health threats, including risk assessments, analysis of epidemiological information, epidemiological modelling, anticipation and forecast, recommendations for actions to prevent and control communicable disease threats and other special health issues, contribution to defining research priorities, and scientific and technical assistance including training and other activities within its mandate;
Amendment 209 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point b a (new) (ba) identify, monitor and collect data on non-communicable diseases which can cause an increase in the incidence, severity and mortality of communicable diseases;
Amendment 210 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 (ba) assess and monitor the impact of communicable diseases on non- communicable diseases, including mental health diseases;
Amendment 211 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point b a (new) (ba) identify possible zoonotic spillovers;
Amendment 212 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point c (c) coordinate the European networking of bodies, organisations and experts operating in the fields within the Centre’s mission, including networks arising from public health activities supported by the Commission and operating the dedicated networks, while ensuring full compliance with the rules on transparency and conflicts of interest;
Amendment 213 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point c (c)
Amendment 214 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point d (d)
Amendment 215 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point e (e) monitor health systems’ capacity and support health administrations in their assessment of the capacity of their health systems relevant to the management of communicable disease threats and other special health issues;
Amendment 216 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point e (e)
Amendment 217 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point e (e) monitor national health systems’ capacity
Amendment 218 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point e (e) monitor and inspect health systems’ capacity relevant to the management of communicable disease threats and other special health issues;
Amendment 219 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point e a (new) (ea) support national monitoring of the response to major communicable diseases to measure progress in tackling them across the Union;
Amendment 220 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point f (f) facilitate the development and implementation of actions, funded by relevant Union funding programmes and instruments, including the implementation of joint actions; in particular the actions of the EU4Health programme 2021-2027 to strengthen the resilience of national health systems to cross-border health threats, and Europe’s Beating Cancer Plan, in view of the well-defined causal links between communicable diseases and the development of cancer (such as the hepatitis B virus and the human papillomavirus).
Amendment 221 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point g (g) provide, upon request of the Commission or the H
Amendment 222 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point g (g) provide, upon request of the Commission
Amendment 223 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point g (g) provide, upon request of the Commission or the HSC, or its own initiative,
Amendment 224 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point g (g) provide, upon request of the Commission or the HSC, or its own initiative, guidelines for surveillance, monitoring, screening, diagnosis, treatment and case management of communicable diseases and other special health issues relevant for public health, in cooperation with relevant societies;
Amendment 225 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point h (h) support epidemic and outbreak response in Member States, and in third countries, in complementarity with other Union emergency response instruments, in particular the Union Civil protection mechanism, by providing recommendations and common provisions on stockpiling of medical countermeasures;
Amendment 226 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point h (h) support epidemic and outbreak response in Member States, and in third countries, in complementarity and close coordination with other Union emergency response instruments, in particular the Union Civil protection mechanism;
Amendment 227 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point h Amendment 228 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point h a (new) (ha) collect information, within its existing infrastructure, on major non- communicable diseases, in particular those whose developments and treatments are impacted significantly by pandemics, such as cancer, diabetes or mental illness;
Amendment 229 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point j (j) provide, upon request of the Commission or the H
Amendment 230 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point j (j) provide, upon request of the Commission
Amendment 231 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 (j) provide, upon request of the Commission or the Health Security Committee (‘HSC’) and in a timely manner, evidence-based communication messages, easily accessible to the public on communicable diseases, on the threats to health posed by them and on the relevant prevention and control measures.
Amendment 232 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point j (j) provide, upon request of the Commission or the Health Security Committee (‘HSC’), or on its own initiative, evidence-based communication messages to the public on communicable diseases, on the threats to health posed by them and on the relevant prevention and control measures.
Amendment 233 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point j (j) provide, upon request of the Commission or the Health Security Committee (‘HSC’), easily accessible and evidence-based communication messages to the public on communicable diseases, on the threats to health posed by them and on the relevant prevention and control measures.
Amendment 234 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point j a (new) (ja) ensure vigilance on modern epidemics such as mental health consequences deriving from communicable diseases, or mental health pathologies such as depression, anxiety, or sleep deprivation.
Amendment 235 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point j a (new) (ja) provide timely information to the Commission, the Member States, the Union agencies and international organisations active within the field of public health;
Amendment 236 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point j b (new) (jb) establish and continually update a database with recognised national competent bodies and public health experts that act within the scope of the mission of the Centre, with relevant data provided by Member States;
Amendment 237 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point j b (new) (jb) cooperate with relevant Union bodies and agencies to help ensure supply chain resilience across the Union;
Amendment 238 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 – point j c (new) (jc) provide recommendations to relevant Union bodies and agencies on how to improve policies under the Health in All Policies principle; those recommendations shall be established done together with the European Environmental Agency;
Amendment 239 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 2 a (new) 2a. In performing its tasks under Article 3(2) of this Regulation, the Centre shall guarantee that its processing operations rigorously respect the data protection principles of lawfulness, fairness and transparency, purpose limitation, data minimisation, accuracy, storage limitation, integrity and confidentiality, as well as the principles of data protection by design and by default as defined in Article 27 of Regulation (EU) 2018/1725, while also determining appropriate technical and organisational security measures in accordance with Article 33 of that Regulation. A Code of Conduct for processing of personal data in accordance with Article 40 of Regulation (EU) 2016/679 shall also be developed.
Amendment 240 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 3 3. The Centre, the Commission, the relevant Union bodies or EU agencies and the Member States shall cooperate with full transparency to promote effective coherence between their respective activities.
Amendment 241 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 3 – subparagraph 1 a (new) The inspections at source shall be organised in each Member State, by an inspector from the body of inspectors appointed by the Centre for a period of four years. Each Member State shall have at least one inspection within the four- year period, but more inspections may be mandated on a case-by-case basis to offer additional support and monitor progress. The results of the inspection in a Member State shall be submitted in a report to the Commission, the European Parliament, the Council and relevant Union agencies. The report shall assess Member State's compliance with the obligations imposed by this Regulation and recommendations from the inspectors in order to improve the situation.
Amendment 242 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 3 a (new) 3a. This Regulation shall be without prejudice to the obligations of Member States relating to their processing of personal data under Regulation (EU) 2016/679 and Directive 2002/58/EC, or the obligations of the Centre and the Commission relating to their processing of personal data under Regulation (EU) 2018/1725, when fulfilling their responsibilities.
Amendment 243 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 3a. The Centre shall put in place procedures and data protection safeguards designed to guarantee that its processing operations fully respect the data protection principles of lawfulness, fairness and transparency, purpose limitation, data minimisation, accuracy, storage limitation, integrity, confidentiality, and data protection by design and by default.
Amendment 244 #
Proposal for a regulation Article 1 – paragraph 1 – point 2 Regulation (EC) No 851/2004 Article 3 – paragraph 3 a (new) 3a. Member States shall ensure without delay the coordination and collaboration with the Centre in relation to all the missions and tasks set out in Article 3.
Amendment 245 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point a (a) communicate to the Centre in a timely manner and according to agreed case definitions, indicators, standards, protocols and procedures data on the surveillance of communicable diseases and other special health issues undertaken in accordance with Article 13 of Regulation (EU) …/… [OJ: please insert the number of Regulation SCBTH [ISC/2020/12524]], and available scientific and technical data and information relevant to the Centre’s mission, including on preparedness, and health systems capacities to detect, prevent, respond to and recover from outbreaks of communicable diseases, complying with the rules laid down by the GDPR and the national rules in force; ;
Amendment 246 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point a (a) communicate to the Centre
Amendment 247 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point a (a) communicate to the Centre in a timely manner and according to agreed case definitions, indicators, standards, protocols and procedures data on the surveillance of communicable diseases and other special health issues undertaken in accordance with Article 13 of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]], and available scientific and technical data and information relevant to the Centre’s mission, including on preparedness, and national health systems capacities to detect, prevent, respond to and recover from outbreaks of communicable diseases;
Amendment 248 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1– point a (a) communicate to the Centre
Amendment 249 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point a a (new) (aa) use at least the indicators referred to in Article 3(2) to assess their domestic health situation and communicate them to the Centre to allow comparability of data;
Amendment 250 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point b (b) notify the Centre of any serious cross-border threats to health, including spread of communicable diseases, unpredicted rise of known or unknown severe non-communicable diseases or chronic conditions and health-related environmental hazards, as soon as detected, through the Early Warning and Response System (EWRS), and promptly communicate response measures taken, as well as any relevant information that may be useful for coordinating the response as referred to in Article 21 of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]]; and
Amendment 251 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point b (b) notify the Centre, in accordance with the general framework developed by the Centre in consultation with the Member States, of any serious cross- border threats to health, as soon as detected, through the Early Warning and Response System (EWRS), and promptly communicate response measures taken, as well as any relevant information that may be useful for coordinating the response as referred to in Article 21 of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]]; and
Amendment 252 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point c (c) identify, within the scope of the mission of the Centre, recognised competent bodies and public health experts who could be made available to assist in Union responses to health threats, such as by undertaking missions to Member States regions and, where necessary, third countries, in order to provide expert advice and field investigations in the event of disease clusters or outbreaks.;
Amendment 253 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point c (c) identify, within the scope of the mission of the Centre, recognised competent bodies and public health experts who could be made available to assist in Union responses to health threats, such as
Amendment 254 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point c (c) identify, within the scope of the mission of the Centre, recognised competent bodies and public health experts and organisations who could be made available to assist in Union responses to health threats, such as by undertaking missions to Member States to provide expert advice and field investigations in the event of disease clusters or outbreaks.;
Amendment 255 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point c a (new) (ca) develop national preparedness and response plans in accordance with Article 6 of Regulation (EU) .../... [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]], update them in a timely manner taking into account the Centre’s recommendations, and report on their preparedness and response planning and implementation at national level in accordance with Article 7 of Regulation (EU) .../... [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]];
Amendment 256 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point c a (new) (ca) ensure the financial means and digital infrastructure for the coordinating competent body and facilitate the mission of the Centre by providing timely the information requested in a standardised format as needed;
Amendment 257 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point c a (new) (ca) promote the automatisation of the data communication process between the national and the Union surveillance systems;
Amendment 258 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point c b (new) (cb) facilitate the digitalisation and the automation of data collection and the data communication process between the national and the Union surveillance systems;
Amendment 259 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – point c c (new) (cc) immediately notify any delay in the reporting of the data to the Centre with an explanation and plan as to when the data will be submitted;
Amendment 260 #
Proposal for a regulation Article 1 – paragraph 1 – point 3 Regulation (EC) No 851/2004 Article 4 – paragraph 1 – subparagraph 1 a (new) Member States shall also, together with the Centre, establish timelines, case definitions, indicators, standards, protocols and procedures for exchange of the information on major non- communicable diseases referred to in point (ha) of Article 3(2).
Amendment 261 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 1 1. The Centre shall support the networking activities of the competent bodies recognised by the Member States through the provision of
Amendment 262 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 1 1. The Centre shall support the networking activities of the competent bodies recognised by the Member States through the provision of coordination and technical and scientific expertise to the Commission and Member States and through the operation of the dedicated networks and other forums that might arise to improve coordination and prevention in relation to health threats.
Amendment 263 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 1 1. The Centre shall support and further develop the networking activities of the competent bodies recognised by the Member States through the provision of coordination and technical and scientific expertise to the Commission and Member States and through the operation of the dedicated networks, making use of the latest digital technologies.
Amendment 264 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 1 The Centre shall ensure the integrated operation of the network for the epidemiological surveillance of the communicable diseases and of the
Amendment 265 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 1 The Centre shall ensure the integrated operation of the network for the epidemiological surveillance of the communicable diseases and non- communicable diseases in accordance with Article 3(2) of this Regulation, and of the related special health issues referred to in points (i) and (ii) of point (a) of Article 2(1) of Regulation (EU) …/… [OJ: Please insert
Amendment 266 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 1 The Centre shall
Amendment 267 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 1 The Centre shall ensure the integrated operation of the network for the epidemiological surveillance of
Amendment 268 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point a (a)
Amendment 269 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point a (a) ensure the further development of the digital platforms and applications supporting epidemiological surveillance at Union level, supporting Member States with technical and scientific advice to establish integrated surveillance systems enabling real-time surveillance where appropriate
Amendment 270 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point a (a) ensure the further development of the digital platforms and applications supporting epidemiological surveillance at Union level,
Amendment 271 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point a (a) ensure the further development of the digital platforms and applications supporting epidemiological surveillance at Union level, supporting Member States with technical and scientific advice to establish integrated surveillance systems enabling real-time surveillance where appropriate, benefiting from existing EU space infrastructures and services; the digital platforms and applications shall be implemented with privacy-enhancing technologies taking into account the state of the art;
Amendment 272 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point a (a) ensure the
Amendment 273 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point a (a) ensure the further development of the digital platforms and applications supporting epidemiological surveillance at Union level, supporting Member States with technical and scientific advice to establish integrated surveillance systems enabling real-time surveillance where appropriate, benefiting from existing EU space infrastructures and services, with the aim to simplify the data exchange process and reduce the administrative burden at Union and Member State levels;
Amendment 274 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point a (a) ensure the further development of the digital platforms and applications supporting epidemiological surveillance at Union level, based on a data protection impact assessment (DPIA) to be conducted prior to their deployment, which shall be used to support
Amendment 275 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point a (a) ensure the further development of the digital platforms and applications supporting epidemiological surveillance at Union level, supporting Member States
Amendment 276 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point a (a)
Amendment 277 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point b (b) adopt specific measures for minimising risks that may emerge from the transfer of bias or incomplete data from multiple sources, as well as establish procedures for data quality review to provide quality assurance by monitoring and evaluating epidemiological surveillance activities (including setting surveillance standards and monitoring data completeness) of the dedicated surveillance
Amendment 278 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point b (b) provide quality assurance by monitoring and evaluating epidemiological surveillance activities (including setting surveillance standards and monitoring data completeness and assessment indicators) of the dedicated surveillance networks to ensure optimal operation;
Amendment 279 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point b (b) provide quality assurance by monitoring and evaluating epidemiological and health surveillance activities (including setting surveillance standards and monitoring data completeness) of the dedicated surveillance
Amendment 280 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2– point c (c) maintain database(s) for such epidemiological surveillance, coordinate with the hosts of other relevant databases, and work towards harmonised approaches to data collection and modelling; in fulfilling this role, the Centre shall minimise the risks that may emerge from the transfer of inaccurate, incomplete or ambiguous data from one database to another, as well as establish robust procedures for data quality review.
Amendment 281 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point c (c) maintain database(s) for such epidemiological surveillance, coordinate with the hosts of other relevant databases, and work towards harmonised approaches to data collection and modelling; in this regard, the Centre shall adopt procedures for data quality review, as well as specific measures for minimising risks that may emerge from the transfer of inaccurate or incomplete data from one database to another;
Amendment 282 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point c (c) maintain database(s) for such epidemiological surveillance, coordinate with the hosts of other relevant databases, and work towards harmonised approaches to data collection and modelling in order to produce harmonised, comparable Union- wide data as a basis for decision-making;
Amendment 283 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point c (c) maintain database(s) for such epidemiological and health surveillance, coordinate with the hosts of other relevant databases,
Amendment 284 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point c a (new) (ca) collect and analyse information provided by Member States on the impact of pandemics on the causes and treatment of relevant major non-communicable diseases;
Amendment 285 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point d (d) communicate the results of the analysis of data to the Commission and Member States and propose communications to inform the public;
Amendment 286 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point d (d) communicate the results of the analysis of data to the Commission and Member States, as well as to the public, where appropriate;
Amendment 287 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – pointe (e) draft, harmonise and rationalise the operating methodologies;
Amendment 288 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point e (e)
Amendment 289 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point f (f)
Amendment 290 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point g (g) ensure the interoperability of the digital platforms for surveillance with digital infrastructures allowing for the
Amendment 291 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point g (g) ensure the interoperability of the digital platforms for surveillance with digital infrastructures allowing for the health data to be used for healthcare, research, policy making and regulatory purposes and with a view to integrate those platforms and infrastructures in the European Health Data Space, as regulated by Union legislation, and make use of other relevant data, for example environmental factors, or phenomena with potential severe health impact at Union or inter-regional level.
Amendment 292 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 (g) ensure the interoperability of the digital platforms for surveillance with digital infrastructures
Amendment 293 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point g (g) ensure the interoperability of the digital platforms for surveillance with digital infrastructures allowing for the health data to be used for healthcare,
Amendment 294 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 2 – subparagraph 2 – point g (g)
Amendment 295 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – introductory part The Centre, through the cooperation of the networks for the epidemiological surveillance, shall:
Amendment 296 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point a (a) monitor and report on trends in communicable diseases and their interconnection to chronic conditions and implications for patients with severe non- communicable diseases and chronic conditions over time and across Member States and in third countries, based on agreed indicators, to assess the present situation and facilitate appropriate evidence-based action, including through the identification of specifications for harmonised data collection from member states
Amendment 297 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point a (a) monitor and report on trends in communicable diseases over time and across Member States and in third countries, based on agreed indicators, to assess the present situation and facilitate appropriate evidence-based action, while respecting the precautionary principle, including through the identification of
Amendment 298 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point a (a) facilitate the monitoring of and report on trends in communicable diseases over time and across Member States and in third countries, based on agreed indicators, to assess the present situation and facilitate appropriate evidence-based action, including through the
Amendment 299 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point c (c) contribute to the evaluation and monitoring of communicable disease prevention and control programmes, as well as prevention and control programmes in relation to major non- communicable diseases, in order to provide the evidence for recommendations to strengthen and improve these programmes at the national
Amendment 300 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point d (d) monitor
Amendment 301 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point d (d)
Amendment 302 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point d (d) monitor and assess health systems’ capacity for diagnosis, prevention and treatment of specific communicable diseases as well as patients’ safety, and provide support to relevant Union bodies and agencies, Member States, and regions and local entities, where appropriate;
Amendment 303 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point d (d) monitor and assess health systems’ capacity for diagnosis, prevention and treatment of specific communicable diseases as well as patients’ safety
Amendment 304 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point d (d) monitor and assess health systems’ capacity, based on standardised indicators and definitions, for diagnosis, prevention and treatment of specific communicable diseases as well as patients’ safety;
Amendment 305 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point d (d) monitor and assess national health systems’ capacity for diagnosis, prevention and treatment of specific communicable diseases as well as patients’ safety;
Amendment 306 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point e (e) identify population groups at risk and in need of targeted prevention and response measures, and e
Amendment 307 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point e (e)
Amendment 308 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point f (f) contribute to the assessment of the burden of communicable diseases on the population using data, such as disease prevalence, complications, hospitalisation and mortality, and ensure that this data is disaggregated on age, gender and disability, as well as contribute to the assessment of the causes and treatment of major non-communicable diseases;
Amendment 309 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point f (f) contribute to the assessment of the burden of communicable diseases on the population using data, such as disease prevalence, complications, clinical links with non-communicable diseases, development of chronic co-morbidities, cancers, hospitalisation and mortality, and ensure that this data is disaggregated on age, gender and disability;
Amendment 310 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point f (f) contribute to the assessment of the burden of communicable diseases on the population using data, such as disease prevalence, complications, hospitalisation and mortality, and ensure that this data is disaggregated on age, gender
Amendment 311 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point f (f)
Amendment 312 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point f (f) contribute to the assessment of the burden of communicable diseases on the population using data, such as disease prevalence, complications, hospitalisation, morbidity and mortality, and ensure that this data is disaggregated on age, gender and disability;
Amendment 313 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point g (g) carry out epidemiological modelling, anticipation and scenario development for response and coordinate such efforts with a view to exchange best practices and improve modelling capacity across the Union, in cooperation with the Member States; and
Amendment 314 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 (h) identify risk factors for disease transmission, including zoonotic transmission, groups most at risk, including the correlation of disease incidence and severity with societal and environmental factors, and research priorities and needs.
Amendment 315 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point h (h) identify, with the Member States, risk factors for disease transmission, groups most at risk, including the correlation of disease incidence and severity with societal and environmental factors, and research priorities and needs.
Amendment 316 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point h Amendment 317 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 4 – point h a (new) (ha) identify, monitor and collect data on non-communicable diseases which can cause increase in the incidence, severity and mortality of communicable diseases;
Amendment 318 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 5 – subparagraph 1 Each Member State shall, on a voluntary basis and in compliance with subsidiarity regarding public health, designate a coordinating competent body and nominate a national focal point and operational contact points as relevant for public health functions, including epidemiological surveillance, and for various disease groups and individual diseases.
Amendment 319 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 5 – subparagraph 2 The national focal points shall form networks that cooperate strategically
Amendment 320 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 5 – subparagraph 3 National focal points and operational contact points nominated for disease- specific interactions with the Centre shall form disease-specific or disease-group- specific networks whose tasks shall include the transmission of national surveillance data as well as mandatory guidelines for the prevention and control of communicable diseases, such as those of zoonotic spillover, to the Centre.
Amendment 321 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 5 – subparagraph 3 National focal points and operational contact points nominated for disease- specific interactions with the Centre shall form disease-specific or disease-group- specific networks whose tasks shall include the transmission of national surveillance data to the Centre, in compliance with subsidiarity and the rules laid down by Regulation (EU) 2016/679 and the national rules in force.
Amendment 322 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 5 –- subparagraph 3 a (new) National focal points shall, to the greatest extent possible, be the same as the National IHR Focal Points, to minimise the duplication of resources and efforts.
Amendment 323 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 6 6. The Centre shall ensure and coordinate the operation of the network of EU reference laboratories referred to in Article 15 of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]], for the diagnosis, detection, identification, genetic sequencing and characterisation of infectious agents that may present a threat to public health.
Amendment 324 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 6 6. The Centre shall
Amendment 325 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 6 a (new) 6a. The Centre shall provide technical and scientific assistance to Member States to develop their detection and sequencing capacities, especially assisting those Member States that do not have sufficient capacities.
Amendment 326 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 8 – subparagraph 1 The Centre shall ensure the operation of the network of Member State services supporting transfusion, transplantation, plasma-derived medicines, and medically assisted reproduction to allow for continuous and rapid access to sero- epidemiological data via sero- epidemiological surveys within the population, including assessment of donor population exposure and immunity. Participation in that network by Member States shall be compulsory.
Amendment 327 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 8 – subparagraph 1 The Centre shall
Amendment 328 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 8 – subparagraph 1 The Centre shall ensure the operation of the network of Member State services supporting transfusion
Amendment 329 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 8 – subparagraph 1 The Centre shall ensure the operation and coordination of the network of Member State services supporting transfusion, transplantation and medically assisted reproduction to allow for continuous and rapid access to sero-
Amendment 330 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 8 – subparagraph 2 The network referred to in the first subparagraph shall support the Centre by monitoring human or animal disease outbreaks that are relevant to substances of human origin and their supply to patients, and with the development of guidelines for blood, tissues and cells safety and quality.
Amendment 331 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 9 9. The Centre shall cooperate with the competent bodies recognised by the Member States and, where applicable, with major public and private research centres, particularly on preparatory work for scientific opinions, scientific and technical assistance, the collection of comparable data based on common formats that allows for ease of aggregation, and the identification of emerging health threats.
Amendment 332 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 Regulation (EC) No 851/2004 Article 5 – paragraph 9 9. The Centre shall cooperate with the competent bodies recognised by the Member States, particularly on preparatory work for scientific opinions, scientific and technical assistance, the collection of comparable data based on agreed common formats that allows for ease of aggregation, and the identification of emerging health threats.
Amendment 333 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5 a – title Prevention of communicable diseases of human or animal origin
Amendment 334 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 1 1. The Centre shall support Member States to strengthen their communicable disease prevention and control systems, improving and facilitating the data collection process with real-time and interoperability sharing of data, as well as capacitating TESSy and other platforms to better address the monitoring and surveillance needs.
Amendment 335 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 1 1. The Centre shall support Member States to strengthen their communicable disease prevention and control systems by providing the scientific advice needed.
Amendment 336 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5 a – paragraph 1 1. The Centre shall support Member States to strengthen their
Amendment 337 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 1 1. The Centre shall support Member States, and regions where appropriate, to strengthen their communicable disease prevention and control systems.
Amendment 338 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 2 2.
Amendment 339 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 2 2. The Centre shall develop a framework for the prevention of communicable diseases and special issues, including vaccine preventable diseases, vaccine hesitancy, antimicrobial resistance, healthcare-associated infections related to communicable diseases, health education, health literacy, health inequalities and behaviour change.
Amendment 340 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 2 2. The Centre shall develop a framework for the prevention of communicable diseases, other health hazards and special issues, including vaccine preventable diseases, antimicrobial resistance, health education, health literacy and behaviour change, with a particular focus on preventive and early action measures.
Amendment 341 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 2 2. The Centre shall develop a framework for the prevention of communicable diseases and special issues, including vaccine preventable diseases, DNA sequencing and gene therapy, antimicrobial resistance, health education, health literacy and behaviour change.
Amendment 342 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 2 2. The Centre shall develop a framework for the prevention of communicable diseases and special issues, including zoonotic spillover, vaccine preventable diseases, antimicrobial resistance, health education, health literacy, mental health and behaviour change.
Amendment 343 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 2 2. The Centre shall develop a
Amendment 344 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph –2 2. The Centre shall
Amendment 345 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 2 2. The Centre shall develop a framework for the prevention of communicable diseases and special issues, including
Amendment 346 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 2 a (new) 2a. The Centre shall provide recommendations to the relevant Union bodies and agencies on how to improve policies under the ‘Health in All Policies’ principle. Those recommendations shall be established together with the European Environment Agency.
Amendment 347 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 3 3. The Centre shall evaluate and monitor communicable disease prevention and control programmes in order to provide the evidence for recommendations to strengthen and improve these programmes at the national and Union level, and where appropriate at the international levels. The Centre shall give binding instructions and guidelines to Member States on the basis of recommendations from the WHO or other relevant international organisations.
Amendment 348 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 3 3. The Centre may, upon request, provide guidelines for creating communicable disease prevention and control programmes, and shall evaluate and monitor communicable disease prevention and control programmes in order to provide the evidence for recommendations to strengthen and improve these programmes at the national and Union level, and where appropriate at the international levels.
Amendment 349 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 3 3. The Centre shall evaluate and monitor communicable disease prevention and control programmes in order to provide the evidence for recommendations to coordinate, strengthen and improve these
Amendment 350 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 3 3. The Centre shall evaluate and monitor communicable disease prevention and control programmes in order to provide the evidence for recommendations to strengthen and improve these programmes at the national and Union level, and where appropriate at international level
Amendment 351 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 3 a (new) 3a. The Centre shall coordinate a multidisciplinary Working Group for Prevention and Early Detection, made up of representatives of the European Environment Agency (EEA), the European Chemicals Agency (ECHA) and the European Food Safety Authority (EFSA), to implement a holistic approach to the prevention and early detection of communicable diseases, systematically integrating the analysis and assessment of risks associated with environmental, climate and food factors with epidemiological surveillance, the weaknesses of national health systems and the concentration of vulnerable groups in the population.
Amendment 352 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 3 a (new) 3a. The Centre shall develop a platform to monitor the vaccination coverage by Member States, taking into account Member States and regional specificities of the vaccination schemes.
Amendment 353 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 3 a (new) 3 a. The Centre shall give Union-wide vaccination recommendations.
Amendment 354 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 4 4. The Centre shall coordinate independent post-marketing vaccines effectiveness and safety monitoring studies collecting new information and/or using the relevant data collected by competent bodies. Besides vaccine-induced immunity, the Centre shall collect data on natural immunity and long-term immunity. That work shall be conducted jointly with the European Medicines Agency and notably though a new vaccine monitoring platform.;
Amendment 355 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 4 4. The Centre
Amendment 356 #
Proposal for a regulation Article 1 – paragraph 1 – point 5 Regulation (EC) No 851/2004 Article 5a – paragraph 4 a (new) 4a. The Centre, in coordination with the European Medicines Agency (EMA), the Commission and the Member States, shall develop initiatives and tools to expand vaccination coverage in Europe, improving the quality and availability of coverage data, and to increase acceptance of vaccines and counter vaccine hesitancy.
Amendment 357 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 1 The Centre shall provide scientific and technical expertise to the Member States and the Commission in collaboration with relevant Union bodies and agencies and the EU integrated political crisis response (IPCR) arrangements and international organisations in accordance with appropriate working arrangements established with the Commission in the field of preparedness and response planning.
Amendment 358 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 1 The Centre shall provide scientific and technical expertise to the Member States and the Commission in collaboration with relevant Union bodies and agencies and international organisations and civil society in accordance with appropriate working arrangements established with the Commission in the field of preparedness and response planning.
Amendment 359 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 1 The Centre shall provide advice and scientific and technical expertise to the Member States and the Commission in collaboration with relevant Union bodies and agencies and international organisations in accordance with appropriate working arrangements established with the Commission in the field of preparedness and response planning.
Amendment 360 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point a (a) contribute to the development, regular review and updating of multi- sectoral preparedness plans and blueprints of multi-sectoral threat-
Amendment 361 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point b (b) develop preparedness monitoring and evaluation frameworks and indicators for preparedness; in this respect the Centre shall give harmonised instructions on the use of common indicators and on actions to be taken in case of serious health hazards, epidemics or pandemics, including in relation to infection rates based on reproduction (R) numbers, in the case of infectious diseases, as a basis for restrictive actions, the harmonised collection of epidemic, diagnostic and mortality data, the use of testing methodologies, quarantines and other restrictions on mobility, and travel and patient isolation requirements; those common indicators shall also cover other health hazards, including chemicals and microplastics in drinking water;
Amendment 362 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point b (b)
Amendment 363 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point c (c) assess and inspect Member States’ preparedness and response planning as well as facilitate self-assessments and external evaluation of Member States’ preparedness and response planning, and contribute to reporting and auditing on preparedness and response planning under Articles 7 and 8 of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]];
Amendment 364 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point c (c) facilitate self-assessments and independent external evaluation of Member States’ preparedness and response planning, and contribute to reporting and auditing on preparedness and response planning under Articles 7 and 8 of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH [ISC/2020/12524]];
Amendment 365 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point c (e) develop exercises, stress tests, in- action and after-action reviews and organise capacity building actions to address identified preparedness capacity and capability gaps;
Amendment 366 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point h (h) develop targeted activities addressing at-risk groups and community preparedness, in particular taking into account the risks associated with the causes and treatment of major non- communicable diseases;
Amendment 367 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point h (h) support the Member States to develop targeted activities addressing at- risk groups and community preparedness;
Amendment 368 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point h (h) develop targeted activities addressing at-risk groups and community- based preparedness models;
Amendment 369 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point i (i) assess health systems’ capacity to detect, prevent, respond to and recover from outbreaks of communicable diseases, identify gaps
Amendment 370 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 (i)
Amendment 371 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point i (i) assess health systems’ capacity based on standardised indicators and definitions to detect, prevent, respond to and recover from outbreaks of communicable diseases, identify gaps and provide recommendations for the strengthening of health systems, to be implemented with Union support as appropriate;
Amendment 372 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 (i) assess national health systems’ capacity to detect, prevent, respond to and recover from outbreaks of communicable diseases, identify gaps and provide recommendations for the strengthening of national health systems, to be implemented with Union support as appropriate;
Amendment 373 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point i (i)
Amendment 374 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point i (i) assess health systems’ capacity, based on set indicators, to detect, prevent, respond to and recover from outbreaks of communicable diseases, identify gaps and provide recommendations for the strengthening of health systems, to be implemented with Union support as appropriate;
Amendment 375 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point i (i) assess and inspect national health systems’ capacity to detect, prevent, respond to and recover from outbreaks of communicable diseases, identify gaps and provide recommendations for the strengthening of health systems, to be implemented with Union support as appropriate
Amendment 376 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point i a (new) (ia) provide recommendations on procurement and minimum quantities needed of medical devices, medicines, therapeutics and personal protective equipment; update such recommendations, where relevant, and supervise the sufficiency of the stocks at Member State level;
Amendment 377 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point i a (new) (ia) publish the assessments of the health systems’ capacity together with the provided recommendations ensuring full transparency;
Amendment 378 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point j (j) bolster modelling, anticipation and forecast capacity of the Centre
Amendment 379 #
Proposal for a regulation Article 1 – paragraph 1 – point 6 Regulation (EC) No 851/2004 Article 5b – paragraph 1 – subparagraph 2 – point k (k) maintain a regular secondment mechanisms between the Centre, the Commission and Member States’ high- level experts.;
Amendment 380 #
Proposal for a regulation Article 1 – paragraph 1 – point 7 – point a Regulation (EC) No 851/2004 Article 6 – paragraph 1a 1a. The Centre shall provide concrete analyses and recommendations for actions to prevent and control communicable disease
Amendment 381 #
Proposal for a regulation Article 1 – paragraph 1 – point 7 – point a Regulation (EC) No 851/2004 Article 6 – paragraph 1a 1a. The Centre shall provide concrete analyses and recommendations for actions to prevent and control communicable diseases or any cross-border health threats upon request of the Commission.
Amendment 382 #
Proposal for a regulation Article 1 – paragraph 1 – point 7 – point b Regulation (EC) No 851/2004 Article 6 – paragraph 3 – subparagraph 1 The Centre may promote and initiate scientific studies necessary for the performance of its mission and applied scientific studies and projects on the feasibility, development and preparation of its activities. The Centre shall avoid duplication with Commission’s, Member States’ and Union research and health programmes, and will liaise between the public health and the research sector
Amendment 383 #
Proposal for a regulation Article 1 – paragraph 1 – point 7 – point b Regulation (EC) No 851/2004 Article 6 – paragraph 3 – subparagraph 1 The Centre may promote and initiate scientific studies necessary for the performance of its mission and applied scientific studies and projects on the feasibility, development and preparation of its activities. The Centre shall avoid duplication with Commission’s, Member States’
Amendment 384 #
Proposal for a regulation Article 1 – paragraph 1 – point 7 – point b Regulation (EC) No 851/2004 Article 6 – paragraph 3 – subparagraph 2 Amendment 385 #
Proposal for a regulation Article 1 – paragraph 1 – point 7 – point b Regulation (EC) No 851/2004 Article 6 – paragraph 3 – subparagraph 2 To carry out the studies referred to in the first paragraph, the Centre shall have access to health data made available or exchanged through digital infrastructures and applications, in accordance with data protection rules, allowing for the health data to be solely used for healthcare, health research, and policy making and regulatory purposes in the domain of health. For the purposes of studies under the first paragraph, the Centre shall also make use of other relevant data, for example on environmental and socio-economic factors, after it has proven the necessity and proportionality of using these data.;
Amendment 386 #
Proposal for a regulation Article 1 – paragraph 1 – point 7 – point b Regulation (EC) No 851/2004 Article 6 – paragraph 3 – subparagraph 2 To carry out the studies referred to in the first paragraph, the Centre shall have access to health data made available or exchanged through digital infrastructures and applications, in accordance with
Amendment 387 #
Proposal for a regulation Article 1 – paragraph 1 – point 7 – point b Regulation (EC) No 851/2004 Article 6 – paragraph 3 – subparagraph 2 To carry out the studies referred to in the first paragraph, the Centre shall have access to health data made available, in compliance with the rules laid down by the GDPR and the national rules in force, or exchanged through digital infrastructures and applications, in accordance with data protection rules, allowing for the health data to be used for healthcare, research, policy making and regulatory purposes. For the purposes of studies under the first paragraph, the Centre shall also make use of other relevant data, for example on environmental and socio-economic factors.;
Amendment 388 #
Proposal for a regulation Article 1 – paragraph 1 – point 7 – point b Regulation (EC) No 851/2004 Article 6 – paragraph 3 – subparagraph 2 To carry out the studies referred to in the first paragraph, the Centre shall have access to health data made available or exchanged through digital infrastructures and applications, in accordance with data protection rules at Union and Member States level, allowing for the health data to be used for healthcare, research, policy making and regulatory purposes. For the purposes of studies under the first paragraph, the Centre shall also make use of other relevant data, for example on environmental and socio-economic factors.;
Amendment 389 #
Proposal for a regulation Article 1 – paragraph 1 – point 7 – point b Regulation (EC) No 851/2004 Article 6 – paragraph 3 – subparagraph 2 a (new) The Centre shall make available the studies referred to in the first subparagraph in a timely manner.
Amendment 390 #
Proposal for a regulation Article 1 – paragraph 1 – point 7 – point b Regulation (EC) No 851/2004 Article 6 – paragraph 3 a (new) 3a. The Centre shall use its own resources, and make use of reference laboratories in order to perform field research and data gathering and data analysis if there is no reliable data available and no research is conducted by other relevant national or Union bodies or agencies.
Amendment 391 #
Proposal for a regulation Article 1 – paragraph 1 – point 7 – point c Regulation (EC) No 851/2004 Article 6 – paragraph 4 4. The Centre shall consult with the Commission
Amendment 392 #
Proposal for a regulation Article 1 – paragraph 1 – point 8 Regulation (EC) No 851/2004 Article 7 – paragraph 1 – introductory part The Centre shall issue an independent scientific opinion on matters falling within its mission:
Amendment 393 #
Proposal for a regulation Article 1 – paragraph 1 – point 8 Regulation (EC) No 851/2004 Article 7 – paragraph 1 – point c (c) at the request of the Commission;
Amendment 394 #
Proposal for a regulation Article 1 – paragraph 1 – point 8 Regulation (EC) No 851/2004 Article 7 – paragraph 1– point c a (new) (ca) at the request of the Health Security Committee
Amendment 395 #
Proposal for a regulation Article 1 – paragraph 1 – point 8 Regulation (EC) No 851/2004 Article 7 – paragraph 2 2. Requests for a scientific opinion referred to in paragraph 1 shall clearly explain the scientific issue to be addressed and the Union interest or necessity and be accompanied by sufficient background information regarding that issue.
Amendment 396 #
Proposal for a regulation Article 1 – paragraph 1 – point 8 Regulation (EC) No 851/2004 Article 7 – paragraph 3 3. The Centre shall issue scientific opinions within a time frame mutually agreed
Amendment 397 #
Proposal for a regulation Article 1 – paragraph 1 – point 8 3. The Centre shall issue scientific opinions
Amendment 398 #
Proposal for a regulation Article 1 – paragraph 1 – point 8 Regulation (EC) No 851/2004 Article 7 – paragraph 4 4. Where different requests are made on the same issue or where the request does not comply with paragraph 2, the Centre may decline to issue a scientific opinion or propose amendments to that request in consultation with the
Amendment 399 #
Proposal for a regulation Article 1 – paragraph 1 – point 8 Regulation (EC) No 851/2004 Article 7 – paragraph 5 5. Where the Centre has already
Amendment 400 #
Proposal for a regulation Article 1 – paragraph 1 – point 8 Regulation (EC) No 851/2004 Article 7 – paragraph 5 a (new) 5a. The Centre shall consult public health experts and relevant organisations, including the Advisory Forum and the WHO, before issuing a scientific opinion.
Amendment 401 #
Proposal for a regulation Article 1 – paragraph 1 – point 9 Regulation (EC) No 851/2004 Article 8 – paragraph 1 1. The Centre shall support and assist the Commission by operating the EWRS and by ensuring with the Member States the capacity to respond in a coordinated manner, particularly in relation to health emergencies and epidemics.
Amendment 402 #
Proposal for a regulation Article 1 – paragraph 1 – point 9 Regulation (EC) No 851/2004 Article 8 – paragraph 1 1. The Centre shall support and assist the Commission by operating the EWRS and by ensuring with the Member States the capacity to respond in a coordinated and timely manner.
Amendment 403 #
Proposal for a regulation Article 1 – paragraph 1 – point 9 Regulation (EC) No 851/2004 Article 8 – paragraph 2 – point b (b) provide information, expertise, advice, training and risk assessment to Member States and the Commission; and
Amendment 404 #
Proposal for a regulation Article 1 – paragraph 1 – point 9 Regulation (EC) No 851/2004 Article 8 – paragraph 2 – point c (c) ensure that the EWRS is efficiently and effectively linked with other Union alert systems, particularly with national alert systems.
Amendment 405 #
Proposal for a regulation Article 1 – paragraph 1 – point 9 Regulation (EC) No 851/2004 Article 8 – paragraph 2 – point c (c) ensure that the EWRS is efficiently and effectively linked with other Union a
Amendment 406 #
Proposal for a regulation Article 1 – paragraph 1 – point 9 Regulation (EC) No 851/2004 Article 8 – paragraph 2 a (new) 2a. The Centre shall work with the Commission, the HSC and Member States to improve the reporting of relevant data through the EWRS, aiming to automate the process and integrate it into national surveillance systems.
Amendment 407 #
Proposal for a regulation Article 1 – paragraph 1 – point 9 Regulation (EC) No 851/2004 Article 8 – paragraph 3 3. The Centre shall work with the Commission and the HSC on the EWRS updates, including for the use of modern technologies, such as digital mobile applications,
Amendment 408 #
Proposal for a regulation Article 1 – paragraph 1 – point 9 3. The Centre shall work with the Commission and the HSC on the EWRS updates, including for the use of modern technologies, such as digital mobile applications, artificial intelligence models, or other technologies for automated contact tracing, building upon the contact tracing technologies developed by the Member States which shall be used for the sole purpose of fighting the pandemic and when proven to be adequate, necessary and proportionate, and in full compliance with Regulation (EU) 2016/679 and Directive 2002/58/EC, and on defining the functional requirements of the EWRS.
Amendment 409 #
Proposal for a regulation Article 1 – paragraph 1 – point 9 Regulation (EC) No 851/2004 Article 8 – paragraph 3 3. The Centre shall work with the Commission and the HSC on the EWRS updates, including for the use of modern technologies, such as digital mobile applications, artificial intelligence and computer modelling and simulation models, or other technologies for automated contact tracing, building upon the contact tracing technologies developed by the Member States and on defining the functional requirements of the EWRS.
Amendment 410 #
Proposal for a regulation Article 1 – paragraph 1 – point 9 Regulation (EC) No 851/2004 Article 8 – paragraph 3 3. The Centre shall work with the Commission and the HSC on the EWRS continuous updates, including for the use of modern technologies, such as digital mobile applications, artificial intelligence models, or other technologies for automated contact tracing, building upon the contact tracing technologies developed by the Member States and on defining the functional requirements of the EWRS.
Amendment 411 #
Proposal for a regulation Article 1 – paragraph 1 – point 9 Regulation (EC) No 851/2004 Article 8 – paragraph 5 5. The Centre
Amendment 412 #
Proposal for a regulation Article 1 – paragraph 1 – point 9 Regulation (EC) No 851/2004 Article 8 – paragraph 5 5. The Centre
Amendment 413 #
Proposal for a regulation Article 1 – paragraph 1 – point 10 Regulation (EC) No 851/2004 Article 8a– paragraph 1 1. The Centre shall provide
Amendment 414 #
Proposal for a regulation Article 1 – paragraph 1 – point 10 Regulation (EC) No 851/2004 Article 8a – paragraph 1 1. The Centre shall provide
Amendment 415 #
Proposal for a regulation Article 1 – paragraph 1 – point 10 Regulation (EC) No 851/2004 Article 8a – paragraph 1 a (new) 1a. Any delay proven through modern and science-informed data in providing the risk assessment may be considered to be wrongful and may be subject to review by the courts.
Amendment 416 #
Proposal for a regulation Article 1 – paragraph 1 – point 10 Regulation (EC) No 851/2004 Article 8a – paragraph 1a (new) 1a. The Centre shall conduct every year a threat analysis for biological agents in order to establish a more harmonised threat and risk perception among all Member States.
Amendment 417 #
Proposal for a regulation Article 1 – paragraph 1 – point 10 Regulation (EC) No 851/2004 Article 8a – paragraph 2 2. The risk assessment
Amendment 418 #
Proposal for a regulation Article 1 – paragraph 1 – point 10 Regulation (EC) No 851/2004 Article 8a – paragraph 2 2. The risk assessment shall include general and targeted recommendations for response as a basis for coordination in the HSC. The Centre shall give binding instructions and guidelines to Member States on the basis of recommendations from the WHO or other relevant international organisations.
Amendment 419 #
Proposal for a regulation Article 1 – paragraph 1 – point 10 Regulation (EC) No 851/2004 Article 8a – paragraph 2 2. The scientific risk assessment shall include general and targeted recommendations for response as a basis for coordination in the HSC.
Amendment 420 #
Proposal for a regulation Article 1 – paragraph 1 – point 10 Regulation (EC) No 851/2004 Article 8a – paragraph 3 3. For the purposes of paragraph 1, the Centre shall coordinate the preparation of rapid risk assessments by involving Member States, public health experts and relevant agencies
Amendment 421 #
Proposal for a regulation Article 1 – paragraph 1 – point 10 Regulation (EC) No 851/2004 Article 8a – paragraph 3 3. For the purposes of paragraph 1, the Centre shall coordinate the preparation of rapid risk assessments by systematically involving Member States experts and relevant agencies
Amendment 422 #
Proposal for a regulation Article 1 – paragraph 1 – point 10 Regulation (EC) No 851/2004 Article 8a – paragraph 4 a (new) 4a. The Centre shall work together with the Member States to improve the risk assessment capacity of the Member States and shall provide training in this area if necessary.
Amendment 423 #
Proposal for a regulation Article 1 – paragraph 1 – point 11 Regulation (EC) No 851/2004 Article 8b – paragraph 1 – point a (a) national responses to the serious cross-border threat to health, including as regards travel restrictions and other restrictions on movement and the gathering of people, as well as quarantine requirements and supervision of quarantines;
Amendment 424 #
Proposal for a regulation Article 1 – paragraph 1 – point 11 Regulation (EC) No 851/2004 Article 8b – paragraph 1 – point a (a) national or inter-regional responses to the serious cross-border threat to health;
Amendment 425 #
Proposal for a regulation Article 1 – paragraph 1 – point 11 Regulation (EC) No 851/2004 Article 8b – paragraph 1 – point a a (new) (aa) Union responses to the serious cross-border threat to health
Amendment 426 #
Proposal for a regulation Article 1 – paragraph 1 – point 11 Regulation (EC) No 851/2004 Article 8b – paragraph 1 – point b (b) adoption of
Amendment 427 #
Proposal for a regulation Article 1 – paragraph 1 – point 11 Regulation (EC) No 851/2004 Article 8b – paragraph 1 – point b a (new) (ba) recommendation for the deployment of the Health Task Force or activation of the Union Civil Protection Mechanism.
Amendment 428 #
Proposal for a regulation Article 1 – paragraph 1 – point 12 – point a Regulation (EC) No 851/2004 Article 9 – paragraph 2 2. The Centre may be requested by the Commission, the Member States, third countries, in particular EU partner countries, and international organisations (in particular the WHO) to provide scientific or technical assistance in any field within the scope of its mission. The
Amendment 429 #
Proposal for a regulation Article 1 – paragraph 1 – point 12 – point c Regulation (EC) No 851/2004 Article 9 – paragraph 6 6. The Centre shall, as appropriate, support and coordinate training programmes, in particular in epidemiological surveillance, field investigations, preparedness and prevention,
Amendment 430 #
Proposal for a regulation Article 1 – paragraph 1 – point 12 – point c Regulation (EC) No 851/2004 Article 9 – paragraph 6 6. The Centre shall, as appropriate, support and coordinate training programmes, in particular in epidemiological surveillance, field investigations, preparedness and prevention, response to public health emergencies, and public health research.;
Amendment 431 #
Proposal for a regulation Article 1 – paragraph 1 – point 12 – point c Regulation (EC) No 851/2004 Article 9 – paragraph 6 6. The Centre shall, as appropriate, support and coordinate training programmes, in particular in epidemiological surveillance, field investigations, preparedness and prevention,
Amendment 432 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point a 1. The Centre shall coordinate data, standardisation, collection, validation, analysis and dissemination of data at Union level.
Amendment 433 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point b Regulation (EC) No 851/2004 Article 11 – paragraph 1a 1a.
Amendment 434 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point b Regulation (EC) No 851/2004 Article 11 – paragraph 1a – point a (a) epidemiological surveillance of communicable diseases, other health threats such as unpredicted rise of known or unknown severe non-communicable diseases or chronic conditions and related special health issues referred to in points (i) and (ii) of point (a) of Article 2(1) of Regulation (EU) …/… [OJ: Please insert the number of Regulation SCBTH
Amendment 435 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point b Regulation (EC) No 851/2004 Article 11 – paragraph 1a – point b (b) the progression of epidemic situations, including for modelling, anticipation and scenario development, the assessment of vulnerable groups and the forecast on specific demand for medicines, equipment and hospital capacity;
Amendment 436 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point b Regulation (EC) No 851/2004 Article 11 – paragraph 1a – point c (c) unusual epidemic phenomena or new communicable diseases of unknown origin, including
Amendment 437 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point b Regulation (EC) No 851/2004 Article 11 – paragraph 1a – point c (c) unusual epidemic phenomena or new communicable and non- communicable diseases of unknown origin, including those in third countries;
Amendment 438 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point b Regulation (EC) No 851/2004 Article 11 – paragraph 1a – point e (e) national health systems data required for managing cross-border health threats.;
Amendment 439 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point b Regulation (EC) No 851/2004 Article 11 – paragraph 1a – point e a (new) (ea) implementation of the Centre’s recommendations on countermeasures by Member States and the outcomes thereof.
Amendment 440 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point b Regulation (EC) No 851/2004 Article 11 – paragraph 1a – point e a (new) (ea) treatment procedures and protocol, as well as case management.
Amendment 441 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point c Regulation (EC) No 851/2004 Article 11 – paragraph 2 – point c (c) work in close cooperation with the competent bodies of the organisations and relevant counterparts operating in the field of data collection from the Union, third countries, the WHO,
Amendment 442 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point c Regulation (EC) No 851/2004 Article 11 – paragraph 2 – point c (c) work in close cooperation with the competent bodies of the organisations operating in the field of data collection from the Union, third countries, the WHO, and other international organisations, ensuring robust safeguards concerning transparency and accountability; and
Amendment 443 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point c Regulation (EC) No 851/2004 Article 11 – paragraph 2 – point c (c) work in close cooperation with the competent bodies of the organisations operating in the field of data collection from the Union, third countries, the WHO, and other international organisations, in full compliance with Regulation (EU) 2018/1725, including Chapter V thereof; and
Amendment 444 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point c Regulation (EC) No 851/2004 Article 11 – paragraph 2 – point d (d) develop solutions to access relevant health data, including anonymous data and pseudonymous data, in line with the principle of data minimisation as defined in point (c) of Article 5(1) of Regulation (EU) 2016/679, where such data are made available or exchanged through digital infrastructures, in accordance with data protection rules, allowing for the health data to be used for healthcare, research, policy making and regulatory purposes; and provide and facilitate controlled access to health data to support public health research.;
Amendment 445 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point c Regulation (EC) No 851/2004 Article 11 – paragraph 2 – point d (d) develop solutions to access relevant health data made available or exchanged through digital infrastructures, in
Amendment 446 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point c Regulation (EC) No 851/2004 Article 11 – paragraph 2 – point d (d) develop solutions to access relevant health data made available or exchanged through digital infrastructures, in accordance with data protection rules
Amendment 447 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point c Regulation (EC) No 851/2004 Article 11 – paragraph 2 – point d (d) develop solutions to access relevant health data made available or exchanged through digital infrastructures, in accordance with data protection rules, allowing for the health data to be solely used for healthcare, health research, and policy making and regulatory purposes in the domain of health; and provide and facilitate controlled access to health data to support public health research.;
Amendment 448 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point d Regulation (EC) No 851/2004 Article 11 – paragraph 4 4. In the situations of urgency related to severity or novelty of a serious cross- border threat to health or to the rapidity of its spread among the Member States, the Centre shall make available epidemiological forecasts as referred to in point (g) of Article 5(4), upon request of the Commission, the European Medicines Agency, or a Member State, in an objective, reliable, transparent and easily accessible way and on the basis of the best available information.
Amendment 449 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point d Regulation (EC) No 851/2004 Article 11 – paragraph 4 4. In the situations of urgency related to severity or novelty of a serious cross- border threat to health or to the rapidity of its spread among the Member States, the Centre shall make available epidemiological forecasts as referred to in point (g) of Article 5(4), upon request of the Commission, Member States or the European Medicines Agency, in an objective, reliable and easily accessible way and on the basis of the best available information.
Amendment 450 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point d Regulation (EC) No 851/2004 Article 11 – paragraph 5 a (new) 5a. The Commission shall adopt delegated acts in accordance with Article [x] to supplement this Regulation by setting out the categories of data subjects under the scope of the processing and the categories of the personal data processed, together with a description of the specific measures to safeguard the rights and freedoms of the data subjects involved in line with relevant data protection legislation, in particular with regard to concrete safeguards to prevent abuse or unlawful access or transfer, and the storage periods.
Amendment 451 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point d Regulation (EC) No 851/2004 Article 11 – paragraph 5 a (new) 5a. This Regulation shall be without prejudice to the obligations of Member States relating to their processing of personal data under Regulation (EU) 2016/679 and Directive 2002/58/EC on privacy and electronic communications, or the obligations of the Centre and the Commission relating to their processing of personal data under Regulation (EU) 2018/1725, when fulfilling their responsibilities.
Amendment 452 #
Proposal for a regulation Article 1 – paragraph 1 – point 13 – point d Regulation (EC) No 851/2004 Article 11 – paragraph 5 b (new) 5b. The Centre shall only process personal data, in particular in the case of health data relating to identified or identifiable individuals, when it is proven to be necessary and proportionate to do so. Whenever possible, in line with the principle of data minimisation, the Centre shall make use of anonymised data, achieved through techniques used such as randomisation or generalisation.
Amendment 453 #
Proposal for a regulation Article 1 – paragraph 1 – point 14 Regulation (EC) No 851/2004 Article 11a – paragraph 1 1. The Centre shall facilitate cooperation between the Member States for the establishment of capacity to mobilise and deploy the EU Health Task Force including the Centre’s staff and experts from Member States and fellowship programmes, to assist local response to outbreaks of communicable diseases in Member States and in third countries.
Amendment 454 #
Proposal for a regulation Article 1 – paragraph 1 – point 14 1. The Centre shall establish a permanent capacity, as well as an enhanced emergency capacity to mobilise and deploy the EU Health Task Force including the Centre
Amendment 455 #
Proposal for a regulation Article 1 – paragraph 1 – point 14 Regulation (EC) No 851/2004 Article 11a – paragraph 1 1. The Centre shall establish capacity to mobilise and deploy the EU Health Task Force including the Centre’s staff
Amendment 456 #
Proposal for a regulation Article 1 – paragraph 1 – point 14 1a. The Centre shall develop capacities to conduct field research and gather relevant data, such as genetic variation of communicable diseases, using the dedicated reference laboratory network or its own resources.
Amendment 457 #
Proposal for a regulation Article 1 – paragraph 1 – point 14 Regulation (EC) No 851/2004 Article 11a – paragraph 2 2. The Centre shall develop a framework and establish procedures with the Commission to
Amendment 458 #
Proposal for a regulation Article 1 – paragraph 1 – point 14 Regulation (EC) No 851/2004 Article 11a – paragraph 2 2. The Centre shall
Amendment 459 #
Proposal for a regulation Article 1 – paragraph 1 – point 14 Regulation (EC) No 851/2004 Article 11a – paragraph 3 3. The Centre shall help to ensure that the EU Health Task Force are coordinated and complementary to the capacities integrating the European Medical Corps and other relevant capacities under the Union Civil Protection Mechanism.
Amendment 460 #
Proposal for a regulation Article 1 – paragraph 1 – point 14 Regulation (EC) No 851/2004 Article 11a – paragraph 4 – subparagraph 1 The Centre shall develop with the Commission a framework for the deployment of the permanent capacity and the mobilisation of the EU Health Task Force, in view of action under Decision No 1313/2013/EU*.
Amendment 461 #
Proposal for a regulation Article 1 – paragraph 1 – point 14 Regulation (EC) No 851/2004 Article 11a – paragraph 4 – subparagraph 1 The Centre shall facilitate the development with the Commission and the Member States of a framework for the mobilisation of the EU Health Task Force, in view of action under Decision No 1313/2013/EU*.
Amendment 462 #
Proposal for a regulation Article 1 – paragraph 1 – point 14 Regulation (EC) No 851/2004 Article 11a – paragraph 5 5. The Centre shall, upon request of the Commission, facilitate the development of field response capabilities and crisis management expertise among the Centre’s staff and experts from EU and EEA countries, EU candidate countries and potential candidates, as well as European Neighbourhood Policy and EU partner countries,
Amendment 463 #
Proposal for a regulation Article 1 – paragraph 1 – point 14 Regulation (EC) No 851/2004 Article 11a – paragraph 6 6. The Centre shall maintain a permanent capacity to carry out missions to Member States, upon request of the Commission and Member States, to provide recommendations on response to threats to health within its mandate.
Amendment 464 #
Proposal for a regulation Article 1 – paragraph 1 – point 15 – point a Regulation (EC) No 851/2004 Article 12 – paragraph 1 – subparagraph 1 The Centre shall communicate on its own initiative within the scope of its mission, after having given prior information to the Member States and to the Commission. The Centre shall ensure that the public or any interested party is rapidly given objective, reliable, evidence-based and easily accessible information with regard to the results of its work, shall share verified information and shall fight against disinformation. The Centre shall make available information for the general public, including through a dedicated online communication portal. It shall also publish its opinions produced in accordance with Article 6.’
Amendment 465 #
Proposal for a regulation Article 1 – paragraph 1 – point 15 – point a Regulation (EC) No 851/2004 Article 12 – paragraph 1 – subparagraph 1 The Centre shall communicate on its own initiative within the scope of its mission, after having given prior information to the Member States
Amendment 466 #
Proposal for a regulation Article 1 – paragraph 1 – point 15 – point a Regulation (EC) No 851/2004 Article 12 – paragraph 1 – subparagraph 1 The Centre shall communicate information about health threats on its own initiative in the fields within its mission, after having given prior information to the Member States and to the Commission.
Amendment 467 #
Proposal for a regulation Article 1 – paragraph 1 – point 15 – point a Regulation (EC) No 851/2004 Article 12 – paragraph 1 – subparagraph 2 Transparency of the Centre’s work enables the public and experts to understand the Centre’s responsibilities and to scrutinise its scientific assessment work and outputs. The Centre shall ensure that the public, healthcare professionals or any interested party is rapidly given objective, reliable, evidence-based and easily accessible information with regard to the results of its work. The Centre shall make available information for the general public, including through a dedicated website with essential information available in all languages of the Union. It shall also publish its opinions produced in accordance with Article 6.;
Amendment 468 #
Proposal for a regulation Article 1 – paragraph 1 – point 15 – point a Regulation (EC) No 851/2004 Article 12 – paragraph 1 – subparagraph 2 The Centre shall ensure that the public or any interested party is rapidly given objective, reliable, evidence-based and easily accessible information with regard to the results of its work. The Centre shall make available information for the general public, including through a dedicated website It shall also publish its opinions produced in accordance with Article 6.; the information communications shall be aligned with the HSC communications.
Amendment 469 #
Proposal for a regulation Article 1 – paragraph 1 – point 15 – point a Regulation (EC) No 851/2004 Article 12 – paragraph 1 – subparagraph 2 The Centre shall ensure that the public or any interested party is
Amendment 470 #
Proposal for a regulation Article 1 – paragraph 1 – point 15 – point b Regulation (EC) No 851/2004 Article 12 – paragraph 2 Amendment 471 #
Proposal for a regulation Article 1 – paragraph 1 – point 15 – point b Regulation (EC) No 851/2004 Article 12 – paragraph 2 (b)
Amendment 472 #
Proposal for a regulation Article 1 – paragraph 1 – point 15 – point b Regulation (EC) No 851/2004 Article 12 – paragraph 2 Amendment 473 #
Proposal for a regulation Article 1 – paragraph 1 – point 15 – point c Regulation (EC) No 851/2004 Article 12 – paragraph 3 3. The Centre shall cooperate as appropriate with the competent bodies in the Member States, the WHO and other interested parties with regard to public information campaigns.;
Amendment 474 #
Proposal for a regulation Article 1 – paragraph 1 – point 16 – point a Regulation (EC) No 851/2004 Article 14 – paragraph 2 – subparagraph 3 Members’ term of office shall be three years and can be extended, if necessary.;
Amendment 475 #
Proposal for a regulation Article 1 – paragraph 1 – point 16 – point b Regulation (EC) No 851/2004 Article 14 – paragraph 5 – point i – subparagraph 1 determine the rules governing the languages of the Centre, including the possibility of a distinction between the internal workings of the Centre and the external communication, taking into account the need to ensure access to, and participation in, the work of the Centre by all interested parties in both cases, as well as expert scrutiny of scientific findings and public understanding of the Centre's work and recommendations.
Amendment 476 #
Proposal for a regulation Article 1 – paragraph 1 – point 16 – point b Regulation (EC) No 851/2004 Article 14 – paragraph 5 – point i – subparagraph 1 determine the rules governing the languages of the Centre, including the possibility of a distinction between the internal workings of the Centre and the external communication, taking into account the need to ensure access to, and participation in, the work of the Centre by all interested parties in both cases. These may include the use of qualified interpreters (sign language, oral or tactile) if needed.
Amendment 477 #
Proposal for a regulation Article 1 – paragraph 1 – point 16 – point b Regulation (EC) No 851/2004 Article 14 – paragraph 5 – point i – subparagraph 1 determine the rules governing the languages of the Centre, including the possibility of a distinction between the internal workings of the Centre and the
Amendment 478 #
Proposal for a regulation Article 1 – paragraph 1 – point 16 – point b Regulation (EC) No 851/2004 Article 14 – paragraph 5 – point i – subparagraph 1 determine by unanimity the rules governing the languages of the Centre, including the possibility of a distinction between the internal workings of the Centre and the external communication, taking into account the need to ensure access to, and participation in, the work of the Centre by all interested parties in both cases.
Amendment 479 #
Proposal for a regulation Article 1 – paragraph 1 – point 19 – point a Regulation (EC) No 851/2004 Article 18 – paragraph 2 2. Members of the Advisory Forum shall not be members of the Management Board. Members’ term of office shall be
Amendment 480 #
Proposal for a regulation Article 1 – paragraph 1 – point 19 – point c Regulation (EC) No 851/2004 Article 18 – paragraph 8 8. The
Amendment 481 #
Proposal for a regulation Article 1 – paragraph 1 – point 19 – point c Regulation (EC) No 851/2004 Article 18 – paragraph 8 8. The director may invite experts or representatives of professional or scientific bodies, or non-governmental organisations, including but not limited to health care professionals, academics and manufacturers, with recognised experience in disciplines related to the work of the Centre to cooperate in specific tasks and to take part in the relevant activities of the Advisory Forum. In addition, the Commission may suggest to the director experts or representatives of professional or scientific bodies, or non- governmental organizations to be invited on an ad-hoc basis.
Amendment 482 #
Proposal for a regulation Article 1 – paragraph 1 – point 20 a (new) Regulation (EC) No 851/2004 Article 20 – paragraph 4 (20a) paragraph 4 of Article 20 is replaced by the following: “4. Personal data shall not be processed or communicated except in cases where this is strictly necessary for the fulfilment of the mission of the Centre. In such cases,
Amendment 483 #
Proposal for a regulation Article 1 – paragraph 1 – point 20 b (new) Regulation (EC) No 851/2004 Article 20 – paragraph 4 a (new) (20b) in Article 20, the following paragraph is added: “4a. This Regulation shall be without prejudice to the obligations of Member States relating to their processing of personal data under Regulation (EU) 2016/679 and Directive 2002/58/EC on privacy and electronic communications, or the obligations of the Centre and the Commission relating to their processing of personal data under Regulation (EU) 2018/1725, when fulfilling their responsibilities.”;
Amendment 484 #
Proposal for a regulation Article 1 – paragraph 1 – point 20 c (new) Regulation (EC) No 851/2004 Article 20 – paragraph 4 b (new) (20c) in Article 20, the following paragraph is added: “4b. The Centre shall adopt specific measures for minimising risks that may emerge from the transfer of inaccurate or incomplete data from Member States’ databases to the Centre, as well as the establishment of procedures for data quality review”;
Amendment 485 #
Proposal for a regulation Article 1 – paragraph 1 – point 21 Regulation (EC) No 851/2004 Article 21 – paragraph 1 – subparagraph 1 Without prejudice to Article 20, the Centre shall not divulge to third parties confidential information that it receives for which confidential treatment has been requested and justified, except for information which must be made public, if circumstances so require, in order to protect public health. If the confidential information has been submitted by a Member State, that information cannot be disclosed without the prior consent of that
Amendment 486 #
Proposal for a regulation Article 1 – paragraph 1 – point 21 Regulation (EC) No 851/2004 Article 21 – paragraph 5 a (new) 5a. The Centre shall ensure the confidentiality of health data under the data protection legislation of Member States and the Union.
Amendment 487 #
Proposal for a regulation Article 1 – paragraph 1 – point 21 Regulation (EC) No 851/2004 Article 21 – paragraph 6 6. The Centre shall develop, deploy and operate an information system capable of exchanging classified and sensitive non- classified information as specified in this Article, in accordance with Articles 27 and 33 of Regulation (EU) 2018/1725.
Amendment 488 #
Proposal for a regulation Article 1 – paragraph 1 – point 21 Regulation (EC) No 851/2004 Article 21 – paragraph 6 a (new) 6a. For the purpose of confidentiality, the Centre shall provide itself with high- quality cybersecurity technology.
Amendment 489 #
Proposal for a regulation Article 1 – paragraph 1 – point 21 Regulation (EC) No 851/2004 Article 21 – paragraph 6 a (new) 6a. All members of the Centre shall be required to demonstrate full personal transparency.
Amendment 490 #
Proposal for a regulation Article 1 – paragraph 1 – point 21 a (new) Regulation (EC) No 851/2004 Article 21 a (new) Amendment 62 #
Proposal for a regulation Recital 1 (1) The Union is committed to
Amendment 63 #
Proposal for a regulation Recital 1 (1) The Union is committed to protect and improve human health, in particular to combat the major cross-border health scourges, measures concerning
Amendment 64 #
Proposal for a regulation Recital 1 (1) The Union is committed to protect and improve human health, in particular to combat the major cross-border health scourges, measures concerning monitoring, early warning of and combating serious cross-border threats to health with significant social impact throughout the Union.
Amendment 65 #
Proposal for a regulation Recital 2 a (new) (2a) The WHO alerted all the Member States on 31 December 2019, but the ECDC did not publicly relay the information until 22 January 2020.
Amendment 66 #
Proposal for a regulation Recital 3 (3) On 11 March 2020, the World Health Organization (WHO) declared the novel coronavirus COVID-19 outbreak a global pandemic
Amendment 67 #
Proposal for a regulation Recital 3 (3) On 11 March 2020, the World Health Organization (WHO) declared the novel coronavirus COVID-19 outbreak a global pandemic. From the challenges experienced in responding to the pandemic it became clear that the Centre’s role in the Union’s framework for health crisis preparedness and response should be strengthened and improved taking into account the lessons learned during the pandemic in order to better use the Centre’s potential to face future outbreaks.
Amendment 68 #
Proposal for a regulation Recital 3 (3) On 11 March 2020, the World
Amendment 69 #
Proposal for a regulation Recital 3 (3) On 11 March 2020, the World Health Organization (WHO) declared the novel coronavirus COVID-19 outbreak a global pandemic which has particularly affected people with chronic non- communicable diseases. From the challenges experienced in responding to the pandemic it became clear that the Centre’s role in the Union’s framework for health crisis preparedness and response should be strengthened.
Amendment 70 #
Proposal for a regulation Recital 3 (3) On 11 March 2020, the World
Amendment 71 #
Proposal for a regulation Recital 3 a (new) (3a) The capacity of the Centre to implement new tasks will depend on the level of financial assistance available from the Union, as well as on available internal and external human resources. In order to be able to fulfil the new tasks entrusted to it in the light of the COVID 19 pandemic, the Centre will need stronger funding and more employees. These new resources cannot come to the Centre only from one-off, project-oriented sources such as the EU4Health programme. From this point of view, the resources already allocated to the Centre in the next multiannual financial framework (‘MFF’) period thus seem to be completely insufficient. It is therefore important that Member States review the MFF and provide the Centre with further new and stable resources to enable it to meet new challenges and develop existing and new activities.
Amendment 72 #
Proposal for a regulation Recital 3 a (new) (3a) Improving overall population health through disease prevention will help to reduce susceptibility to future infectious outbreaks. Given the links between non-communicable and communicable diseases, an important part of communicable disease control requires consideration of non-communicable diseases. Furthermore, as many outbreaks are of zoonotic origin, a One Health approach is needed considering the interactions between humans, animals and the environment in order to face the emerging threats of zoonotic diseases.
Amendment 73 #
Proposal for a regulation Recital 5 (5) This Regulation
Amendment 74 #
Proposal for a regulation Recital 5 (5) This Regulation accordingly expands the mission and tasks of the Centre to enhance the Centre’s capacity to provide the required scientific expertise and to support actions which are relevant to the prevention, preparedness, response planning and combating serious cross- border threats to health in the Union, including cross-border threats, communicable diseases and major chronic diseases and especially the interconnections between them, in accordance with Regulation EU …/… of the European Parliament and of the Council10 [ISC/2020/12524]. __________________ 10Regulation (EU) XXXX/XXXX of the European Parliament and of the Council of DATE on serious cross-border threats to health and repealing Decision No 1082/2013/EU [OJ: please, insert full title and publication reference to Regulation on serious cross border threats to health (SCBTH).]
Amendment 75 #
Proposal for a regulation Recital 5 (5) This Regulation accordingly expands the mission and tasks of the Centre to enhance the Centre’s capacity to provide the required robust and independent scientific expertise and to support actions which are relevant to the prevention, preparedness, response planning and combating serious cross- border threats to health in the Union in accordance with Regulation EU …/… of the European Parliament and of the Council10 [ISC/2020/12524]. __________________ 10Regulation (EU) XXXX/XXXX of the European Parliament and of the Council of DATE on serious cross-border threats to health and repealing Decision No 1082/2013/EU [OJ: please, insert full title and publication reference to Regulation on serious cross border threats to health (SCBTH).]
Amendment 76 #
Proposal for a regulation Recital 5 a (new) (5a) The European Ombudsman's decision of 5 February2021 in strategic inquiry OI/3/2020/TE identified some important effectiveness gaps in the Centre's response to the COVID-19 pandemic, as regards how the Centre gathers information, the transparency of that information and how it communicates with the public, as well as a power asymmetry between the Centre and the Member States, resulting in lack of timely, complete and comparable data and thus affecting the modelling and forecasting potential of the Centre, which should be addressed in this Regulation.
Amendment 77 #
Proposal for a regulation Recital 5 a (new) (5a) The European Ombudsman’s decision of 5 February2021 in strategic inquiry OI/3/2020/TE highlighted shortcomings in how the data is communicated and gathered by the Centre during the COVID-19 crisis. Notably, there were discrepancies in the reporting of reliable data and the lack of such data directly affected the Centre’s modelling and forecasting capacity. These issues and others have impeded the important work by the Centre and this Regulation should strengthen the mandate further to ensure inter alia improved coordination, epidemiological surveillance and communication.
Amendment 78 #
Proposal for a regulation Recital 6 (6) In this respect, the Centre should be tasked with providing epidemiological information and its analysis, epidemiological modelling, anticipation and drafting forecast
Amendment 79 #
Proposal for a regulation Recital 6 (6) In this respect, the Centre should be tasked with providing epidemiological information and its analysis, epidemiological modelling, anticipation and forecasting, relevant risk assessments and recommendations, which set out options for prevention and control of communicable diseases. Its actions should be consistent with a One-Health
Amendment 80 #
Proposal for a regulation Recital 6 (6) In this respect, the Centre should be tasked with providing epidemiological information and its analysis, epidemiological modelling, anticipation and forecasting, relevant risk assessments and recommendations, which set out options for prevention and control of communicable diseases, prevention of excess mortality among patients, notably those suffering from chronic diseases and the increase of infection-caused chronic diseases and other pathogens associated with chronic diseases. This should also contribute to efficiently responding to current and emerging threats to human health posed by non-communicable diseases, either directly or indirectly, due to increasing risks associated with communicable diseases. Its actions should be consistent with a One-Health approach, recognising the interconnections between communicable and chronic diseases, as well as between human and animal health and the environment. It should monitor the capacity of the national health systems to respond to communicable disease threats, in particular given the importance of this information in the preparation of the national preparedness and response plans, with a view to enabling Member States to better assess their health systems' capacities. The Centre should support the implementation of actions funded by the relevant Union funding programmes and instruments and related to communicable diseases, including their interconnection with chronic diseases, provide guidelines for treatment and case management based on a thorough assessment of the latest evidence, support epidemic and outbreak responses in Member States and third countries, including field response, and provide timely objective, reliable and easily accessible information on communicable diseases and their effect on the health-related quality of life of patients with chronic diseases to the public. The Centre should also establish clear procedures for cooperation with the public health actors in third countries, as well as international organisations competent in the field of public health hence contributing to EU’s
Amendment 81 #
Proposal for a regulation Recital 6 (6) In this respect, the Centre should be tasked with providing epidemiological information and its analysis, epidemiological modelling, anticipation and forecasting, relevant risk assessments and recommendations, which set out options for prevention and control of communicable diseases. Its actions should be consistent with a One- Health approach, as well as with the Health in All Policies principle, recognising the interconnections between human and animal health and the
Amendment 82 #
Proposal for a regulation Recital 6 (6) In this respect, the Centre should be tasked with providing epidemiological information and its analysis, epidemiological modelling, anticipation and forecasting, relevant risk assessments and recommendations, which set out options for prevention and control of communicable diseases. Its actions should be consistent with a One-Health approach, recognising the interconnections between human and animal health and the environment. It should monitor the capacity of the national health systems to respond to communicable disease threats, in particular given the importance of this information in the preparation of the national preparedness and response plans. The monitoring of the health systems’ capacity should be based on standardised indicators and definitions in order to ensure comparability. When assessing Member States’ health systems capacity, the Centre should inter alia take into account reported health indicators by Eurostat. To the greatest extent possible, the Centre should further explore possible synergies with the work on health systems performance assessment, in particular by the Commission, the OECD and the WHO. The Centre should support the implementation of actions funded by the relevant Union funding programmes and instruments and related to communicable diseases, provide guidelines for treatment and case management based on a thorough assessment of the latest evidence, support epidemic and outbreak responses in Member States and third countries, including field response, and provide timely objective, reliable and easily accessible information on communicable diseases to the public. The Centre should also establish clear procedures for cooperation with the public health actors in third countries, as well as international organisations competent in the field of public health hence contributing to EU’s commitment to reinforcing partners’ preparedness and response capacity.
Amendment 83 #
Proposal for a regulation Recital 6 (6) In this respect, the Centre should be tasked with providing epidemiological information and its analysis, epidemiological modelling, anticipation and forecasting, relevant risk assessments and recommendations, which set out options for prevention and control of communicable diseases. Its actions should be consistent with a One-Health approach, recognising the interconnections between human and animal health and the environment. It should monitor, evaluate and support the capacity of the national health systems to respond to communicable disease threats, in particular given the importance of this information in the preparation of the national preparedness and response plans. Such plans should include recommendations for policy interventions related to mitigation of the impact of communicable diseases on health services and care, including for non-communicable diseases. The Centre should support the implementation of actions funded by the relevant Union funding programmes and instruments and related to communicable diseases, provide guidelines for treatment and case management based on a thorough assessment of the latest evidence, support epidemic and outbreak responses in Member States and third countries, including field response, and provide timely objective, reliable and easily accessible information on communicable diseases to the public. The Centre should also establish clear procedures for cooperation with the public health actors in third countries, as well as international
Amendment 84 #
Proposal for a regulation Recital 6 (6) In this respect, the Centre should be tasked with providing epidemiological information and its analysis, epidemiological modelling, anticipation and forecasting, relevant risk assessments and recommendations, which set out options for prevention and control of communicable diseases. Its actions should be consistent with a One-Health approach, recognising the interconnections between human and animal health and the environment, taking into account the fact that approximately 60% of communicable human diseases are of animal origin and that more work and resources should be dedicated to preventing and researching zoonotic diseases. It should monitor the capacity of the national health systems to respond to communicable disease threats, in particular given the importance of this information in the preparation of the national preparedness and response plans. The Centre should support the implementation of actions funded by the relevant Union funding programmes and instruments and related to communicable diseases, provide guidelines for treatment and case management based on a thorough assessment of the latest evidence, support epidemic and outbreak responses in Member States and third countries,
Amendment 85 #
Proposal for a regulation Recital 6 (6) In this respect, the Centre should be tasked with providing as quickly as possible epidemiological information and its analysis, epidemiological modelling, anticipation and forecasting, relevant risk assessments and recommendations, which set out options for prevention and control of communicable diseases. Its actions should be consistent with a One-Health approach, recognising the interconnections between human and animal health and the environment, particularly in view of the most recent human or animal epidemics. It should monitor the capacity of the national health systems to respond to communicable disease threats, in particular given the importance of this information in the preparation of the national preparedness and response plans. The Centre should support the implementation of actions funded by the relevant Union funding programmes and
Amendment 86 #
Proposal for a regulation Recital 6 (6) In this respect, the Centre should be tasked with providing epidemiological information and its analysis, epidemiological modelling, anticipation and forecasting, establishing applicable risk indicators and providing relevant risk assessments and recommendations, which set out options for prevention and control of communicable diseases. Its actions should be consistent with a One-Health approach, recognising the interconnections between human and animal health and the environment. It should monitor and inspect periodically the capacity of the national health systems to respond to communicable disease threats, in particular given the importance of this information in the preparation of the
Amendment 87 #
Proposal for a regulation Recital 6 (6) In this respect, the Centre should be tasked with providing epidemiological information and its analysis, epidemiological modelling, anticipation and forecasting, relevant risk assessments and recommendations, which set out options for prevention and control of communicable diseases. Its actions should be consistent with a One-Health approach, recognising the interconnections between human and animal health and the environment. It should monitor the
Amendment 88 #
Proposal for a regulation Recital 6 a (new) (6a) In order to have high-performing health systems accessible for all, there is a need for a holistic approach to public health. The Centre should be tasked with the monitoring of non-communicable diseases and of the impact that infectious diseases have on health systems at large. Based on the Centre's vast experience with Union-level surveillance and monitoring of communicable diseases, its existing tool for data collection (TESSy) and its links to national public health bodies responsible for both communicable and non-communicable diseases, the Centre is in a unique position to deliver effectively a one-stop-shop for health information that can be used for policy decision-making.
Amendment 89 #
Proposal for a regulation Recital 6 a (new) (6a) Ensuring supply chain resilience across the Union is not a primordial mission of the Centre, yet the Centre should provide data, knowledge, and skills, to the Commission and the European Medicines Agency in order to ensure supply chain resilience in the Union. Supply chain resilience is part of the four working groups of the COVID– 19 taskforce of the European Medicines Agency, alongside the therapeutic response, business continuity and impact, and human resources.
Amendment 90 #
Proposal for a regulation Recital 6 a (new) (6a) Taking into account the clear links between communicable and non- communicable diseases and a need for a truly integrated approach to health, the Centre should be tasked with the identification and monitoring of the relationship between non-communicable and communicable diseases considering the substantial effect of comorbidities on health outcomes as observed during the COVID-19 pandemic.
Amendment 91 #
Proposal for a regulation Recital 7 (7) Access to timely and complete data is a precondition for the Centre to conduct rapid risk assessments, including epidemiological modelling and forecasting. To effectively support the work of the Centre and ensure the fulfilment of its mission, Member States should
Amendment 92 #
Proposal for a regulation Recital 7 (7) To effectively support the work of the Centre and ensure the fulfilment of its mission, Member States should be tasked to communicate to the Centre data on the surveillance and monitoring of communicable diseases, the interconnection with chronic conditions and other special health issues such as antimicrobial resistance and health care- associated infections related to communicable diseases, as well as broader health determinants including social determinants, available scientific and technical data and information relevant to the Centre’s mission, to notify the Centre of any serious cross-border threats to health, information on preparedness and response planning and health system capacity, and provide relevant information that may be useful for coordinating the response, as well as identify recognised competent bodies and public health experts available to assist in Union responses to health threats. All timelines, case definitions, indicators, standards, protocols and procedures for communication adopted by the Centre should be agreed with Member States and be mandatory for the Member States thereafter.
Amendment 93 #
Proposal for a regulation Recital 7 (7) To effectively support the work of the Centre and ensure the fulfilment of its mission, Member States
Amendment 94 #
Proposal for a regulation Recital 7 (7) To effectively support the work of the Centre and ensure the fulfilment of its mission, Member States should be tasked to communicate continuously and comprehensively to the Centre data on the surveillance of communicable diseases and other special health issues such as antimicrobial resistance and healthcare- associated infections related to communicable diseases, available scientific and technical data and information relevant to the Centre’s mission, to notify the Centre rapidly of any serious cross-border threats to health, information on preparedness and response planning and actual health system capacity to address the threat and its possible consequences, and provide relevant information that may be useful for coordinating the response, as well as identify recognised competent bodies and public health experts available to assist in Union responses to health threats.
Amendment 95 #
Proposal for a regulation Recital 7 (7) To effectively support the work of the Centre and ensure the fulfilment of its mission, Member States should be tasked to communicate in a timely manner to the Centre complete data on the surveillance of communicable diseases and other special health issues such as antimicrobial resistance and healthcare-
Amendment 96 #
Proposal for a regulation Recital 7 a (new) (7a) Member States, the Commission and the Centre shall identify recognised competent bodies and public health experts, both in the areas of communicable and of non-communicable diseases, available to assist in Union responses to health threats. Such experts and stakeholders, including civil society organisations, should be structurally engaged throughout all activities of the Centre and contribute to its advice and decision-making processes. Full compliance with transparency and conflict of interest rules for stakeholder engagement should be ensured.
Amendment 97 #
Proposal for a regulation Recital 7 a (new) (7a) The Centre should keep a thorough vigilance on modern epidemics such as mental health consequences deriving from communicable diseases, or mental health pathologies such as depression, anxiety, or sleep deprivation. In this regard, the Centre should follow up and share information with the Member States and the regions on how to improve the situation.
Amendment 98 #
Proposal for a regulation Recital 7 a (new) (7a) In order to facilitate the analysis of information provided by the Member States, the Centre, working together with the Member States, should establish an overall framework identifying the elements required for this analysis to enable the information provided to be harmonised and to facilitate decision- making.
Amendment 99 #
Proposal for a regulation Recital 7 a (new) (7a) The Centre should provide guidelines to Member States on standardising collection and communication of relevant data.
source: 691.216
|
History
(these mark the time of scraping, not the official date of the change)
docs/4 |
|
docs/6 |
|
events/9 |
|
events/12 |
|
events/13 |
|
events/13/summary |
|
events/12 |
|
procedure/final |
|
procedure/stage_reached |
Old
Procedure completed, awaiting publication in Official JournalNew
Procedure completed |
events/11 |
|
procedure/stage_reached |
Old
Awaiting signature of actNew
Procedure completed, awaiting publication in Official Journal |
docs/0 |
|
docs/7 |
|
docs/7/date |
Old
2021-03-24T00:00:00New
2021-03-23T00:00:00 |
docs/8 |
|
docs/8 |
|
docs/8/date |
Old
2021-05-19T00:00:00New
2021-05-18T00:00:00 |
docs/9 |
|
docs/9 |
|
docs/9/date |
Old
2021-02-15T00:00:00New
2021-02-14T00:00:00 |
docs/10 |
|
events/0 |
|
docs/0 |
|
docs/7 |
|
docs/8 |
|
docs/8 |
|
docs/8/date |
Old
2021-03-23T00:00:00New
2021-03-24T00:00:00 |
docs/9 |
|
docs/9 |
|
docs/9/date |
Old
2021-05-18T00:00:00New
2021-05-19T00:00:00 |
docs/10 |
|
docs/10/date |
Old
2021-02-14T00:00:00New
2021-02-15T00:00:00 |
events/0 |
|
events/7 |
|
events/7/docs |
|
events/8 |
|
docs/0 |
|
docs/7 |
|
docs/7/date |
Old
2021-03-24T00:00:00New
2021-03-23T00:00:00 |
docs/8 |
|
docs/8 |
|
docs/8/date |
Old
2021-05-19T00:00:00New
2021-05-18T00:00:00 |
docs/9 |
|
docs/9 |
|
docs/9/date |
Old
2021-02-15T00:00:00New
2021-02-14T00:00:00 |
docs/10 |
|
events/0 |
|
docs/0 |
|
docs/6 |
|
docs/7 |
|
docs/7 |
|
docs/8 |
|
docs/8 |
|
docs/8/date |
Old
2021-03-23T00:00:00New
2021-03-24T00:00:00 |
docs/9 |
|
docs/9/date |
Old
2021-05-18T00:00:00New
2021-05-19T00:00:00 |
docs/10 |
|
docs/10/date |
Old
2021-02-14T00:00:00New
2021-02-15T00:00:00 |
events/0 |
|
events/10 |
|
procedure/stage_reached |
Old
Awaiting Council's 1st reading positionNew
Awaiting signature of act |
docs/0 |
|
docs/6 |
|
docs/6/date |
Old
2021-03-24T00:00:00New
2021-03-23T00:00:00 |
docs/7 |
|
docs/7 |
|
docs/7/date |
Old
2021-05-19T00:00:00New
2021-05-18T00:00:00 |
docs/8 |
|
docs/8 |
|
docs/8/date |
Old
2021-02-15T00:00:00New
2021-02-14T00:00:00 |
docs/9 |
|
docs/10 |
|
events/0 |
|
events/8 |
|
events/9 |
|
events/9/summary |
|
docs/0 |
|
docs/7 |
|
docs/8 |
|
docs/8 |
|
docs/8/date |
Old
2021-03-23T00:00:00New
2021-03-24T00:00:00 |
docs/9 |
|
docs/9 |
|
docs/9/date |
Old
2021-05-18T00:00:00New
2021-05-19T00:00:00 |
docs/10 |
|
docs/10/date |
Old
2021-02-14T00:00:00New
2021-02-15T00:00:00 |
events/0 |
|
docs/4 |
|
docs/6 |
|
events/8 |
|
events/9 |
|
forecasts |
|
procedure/stage_reached |
Old
Awaiting Parliament's position in 1st readingNew
Awaiting Council's 1st reading position |
forecasts/0 |
|
forecasts/1 |
|
forecasts |
|
docs/0 |
|
docs/5 |
|
docs/5/date |
Old
2021-03-24T00:00:00New
2021-03-23T00:00:00 |
docs/6 |
|
docs/6 |
|
docs/6/date |
Old
2021-05-19T00:00:00New
2021-05-18T00:00:00 |
docs/7 |
|
docs/7 |
|
docs/7/date |
Old
2021-02-15T00:00:00New
2021-02-14T00:00:00 |
docs/8 |
|
events/0 |
|
docs/0 |
|
docs/5 |
|
docs/6 |
|
docs/6 |
|
docs/6/date |
Old
2021-03-23T00:00:00New
2021-03-24T00:00:00 |
docs/7 |
|
docs/7 |
|
docs/7/date |
Old
2021-05-18T00:00:00New
2021-05-19T00:00:00 |
docs/8 |
|
docs/8/date |
Old
2021-02-14T00:00:00New
2021-02-15T00:00:00 |
events/0 |
|
docs/5/docs/0/url |
Old
http://www.connefof.europarl.europa.eu/connefof/app/exp/COM(2020)0726New
https://connectfolx.europarl.europa.eu/connefof/app/exp/COM(2020)0726 |
docs/6/docs/0/url |
Old
http://www.connefof.europarl.europa.eu/connefof/app/exp/COM(2020)0726New
https://connectfolx.europarl.europa.eu/connefof/app/exp/COM(2020)0726 |
docs/7 |
|
docs/3/docs/0/url |
https://dmsearch.cor.europa.eu/search/public?k=(documenttype:AC)(documentnumber:5624)(documentyear:2020)(documentlanguage:EN)
|
procedure/subject/4.20.01 |
Medicine, diseases
|
docs/0 |
|
docs/5 |
|
docs/5/date |
Old
2021-03-24T00:00:00New
2021-03-23T00:00:00 |
docs/6 |
|
docs/6 |
|
docs/6/date |
Old
2021-05-19T00:00:00New
2021-05-18T00:00:00 |
docs/7 |
|
events/0 |
|
procedure/subject/4.20.01 |
Medicine, diseases
|
events/6 |
|
docs/6 |
|
events/4/summary |
|
docs/6 |
|
events/4 |
|
events/5 |
|
forecasts |
|
events/3/docs |
|
events/3 |
|
forecasts/0 |
|
forecasts/0/title |
Old
Indicative plenary sitting dateNew
Debate in plenary scheduled |
forecasts/1 |
|
docs/5 |
|
events/2/docs |
|
events/2 |
|
procedure/stage_reached |
Old
Awaiting committee decisionNew
Awaiting Parliament's position in 1st reading |
events/2 |
|
procedure/stage_reached |
Old
Awaiting Parliament's position in 1st readingNew
Awaiting committee decision |
events/2 |
|
procedure/stage_reached |
Old
Awaiting committee decisionNew
Awaiting Parliament's position in 1st reading |
events/1 |
|
procedure/Other legal basis |
Rules of Procedure EP 159
|
docs/4 |
|
forecasts/0/date |
Old
2021-07-05T00:00:00New
2021-09-13T00:00:00 |
docs/0 |
|
docs/5 |
|
events/0 |
|
docs/2 |
|
docs/2 |
|
docs/2 |
|
events/1/body |
EP
|
docs/0 |
|
docs/1 |
|
docs/1/docs/0/url |
https://www.europarl.europa.eu/doceo/document/ENVI-AM-691216_EN.html
|
docs/2 |
|
docs/2 |
|
events/0 |
|
forecasts/0/title |
Old
Indicative plenary sitting date, 1st reading/single readingNew
Indicative plenary sitting date |
procedure/title |
Old
Public health: European Centre for disease prevention and controlNew
European Centre for Disease Prevention and Control |
docs/0 |
|
docs/0 |
|
docs/1 |
|
docs/1 |
|
docs/1/docs/0/url |
Old
https://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE681.065New
https://www.europarl.europa.eu/doceo/document/ENVI-PR-681065_EN.html |
docs/2 |
|
docs/2/date |
Old
2021-04-07T00:00:00New
2021-04-13T00:00:00 |
events/0 |
|
events/0 |
|
events/1 |
|
docs/1/date |
Old
2021-03-30T00:00:00New
2021-04-07T00:00:00 |
docs/1 |
|
forecasts |
|
committees/0 |
|
committees/0 |
|
committees/1 |
|
committees/1 |
|
docs/0/docs/0/url |
https://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE681.065
|
docs/0 |
|
docs/0 |
|
committees/0 |
|
committees/0 |
|
committees/1 |
|
committees/1 |
|
committees/0 |
|
committees/0 |
|
committees/1 |
|
committees/1 |
|
committees/0 |
|
committees/0 |
|
committees/1 |
|
committees/1 |
|
events/1 |
|
procedure/Legislative priorities |
|
procedure/dossier_of_the_committee |
|
procedure/stage_reached |
Old
Preparatory phase in ParliamentNew
Awaiting committee decision |
commission |
|
committees/0/shadows/0/mepref |
197584
|
committees/1/rapporteur |
|
events/0/summary |
|
committees/0/shadows |
|
otherinst |
|
procedure/other_consulted_institutions |
European Economic and Social Committee European Committee of the Regions
|