2019/2078(DEC) 2018 discharge: European Food Safety Authority (EFSA)
Next event: Indicative plenary sitting date, 1st reading/single reading 2020/03/31
Lead committee dossier:
Next event: Indicative plenary sitting date, 1st reading/single reading 2020/03/31
Progress: Awaiting Parliament's vote
Role | Committee | Rapporteur | Shadows |
---|---|---|---|
Lead | CONT | CZARNECKI Ryszard ( ECR) | NOVAKOV Andrey ( EPP), WOLTERS Lara ( S&D), CSEH Katalin ( Renew), KUHS Joachim ( ID), EICKHOUT Bas ( Verts/ALE), OMARJEE Younous ( GUE/NGL) |
Committee Opinion | ENVI | CANFIN Pascal ( Renew) | Stanislav POLČÁK ( PPE) |
Lead committee dossier:
Subjects
Events
2020/03/31
Indicative plenary sitting date, 1st reading/single reading
2020/03/03
EP - Committee report tabled for plenary, single reading
2020/02/19
EP - Vote in committee, 1st reading/single reading
2020/02/06
CSL - Supplementary non-legislative basic document
Documents
2020/01/31
EP - Amendments tabled in committee
Documents
2020/01/22
EP - Committee opinion
Documents
2019/12/05
EP - Committee draft report
Documents
2019/10/01
EP - CZARNECKI Ryszard (ECR) appointed as rapporteur in CONT
2019/09/18
EP - Committee referral announced in Parliament, 1st reading/single reading
2019/09/04
EP - CANFIN Pascal (Renew) appointed as rapporteur in ENVI
2019/06/27
EC - Non-legislative basic document
Documents
2019/06/27
EC - Non-legislative basic document published
Documents
Documents
- Supplementary non-legislative basic document: 05761/2020
- Amendments tabled in committee: PE646.781
- Committee opinion: PE641.158
- Committee draft report: PE639.854
- Non-legislative basic document: COM(2019)0316
- Non-legislative basic document: EUR-Lex
- Non-legislative basic document published: COM(2019)0316
- Non-legislative basic document published: EUR-Lex
- Non-legislative basic document: COM(2019)0316 EUR-Lex
- Committee draft report: PE639.854
- Committee opinion: PE641.158
- Amendments tabled in committee: PE646.781
- Supplementary non-legislative basic document: 05761/2020
Amendments | Dossier |
11 |
2019/2078(DEC)
2019/12/11
ENVI
11 amendments...
Amendment 1 #
Draft opinion Paragraph 4 a (new) 4 a. Notes with concern that the Authority, as one of the Union regulatory agencies responsible for risk assessment of regulated products, does not receive sufficient resources to carry out effectively its responsibilities; insists that the Authority is granted sufficient resources to carry out its tasks;
Amendment 10 #
Draft opinion Paragraph 8 8. Notes that following the results of the third external evaluation of the Authority, the Management Board adopted a series of recommendations, focusing on enhancing the Authority’s capacity for fit- for-purpose scientific advice, bolstering communication activities to strengthen the Authority’s reputation and securing the long-term efficiency and sustainability of the Authority’s operations; stresses the need to ensure the Authority's independence, given that some of its officials have been accused of having conflicts of interest and connections with the companies whose products it was supposed to be monitoring, and, in some cases, passing on arguments from their internal scientific reports;
Amendment 11 #
Draft opinion Paragraph 9 9. Notes with satisfaction that the Authority cooperates with other agencies working on complementary tasks, i.e. the European Centre for Disease Prevention and Control (ECDC), the European Chemicals Agency and the European Medicines Agency, e.g. in the areas of data collection and analysis and databases (e.g. zoonoses, antimicrobial resistance, molecular typing), in scientific assessments (e.g. rapid outbreak assessments with the ECDC), or risk assessment; stresses the importance of cooperation at EU and international level, including with Member States, EU bodies and institutions, scientific organisations, international organisations, and third countries;
Amendment 2 #
Draft opinion Paragraph 6 6. Believes that the Authority should continue paying special attention to public opinion, and commit itself to openness and transparency;
Amendment 3 #
Draft opinion Paragraph 6 6. Believes that the Authority should continue paying special attention to public opinion, and commit itself to increased openness and increased transparency;
Amendment 4 #
Draft opinion Paragraph 6 6. Believes that the Authority should continue paying special attention to public
Amendment 5 #
Draft opinion Paragraph 7 7. Welcomes that, following adoption of its new policy on independence in 2017,
Amendment 6 #
Draft opinion Paragraph 7 a (new) 7 a. Regrets that, in relation to the two- year cooling-off period, the 2017 independence policy includes the obligation to screen experts' interests only in relation to the mandate of the scientific group to which the expert is applying; calls for the policy to be updated without delay in order to ensure that experts' interests are viewed within the context of the overall remit of the Authority, as repeatedly called for by Parliament;
Amendment 7 #
Draft opinion Paragraph 7 b (new) 7 b. Regrets that the research funding from companies in the Authority's remit is not considered relevant to the cooling-off period as long as amounts at stake do not rise above 25 % of the total research budget managed by the expert and/or their research team, and that the threshold is applied to individual sources as opposed to all private sources combined; calls for the funding threshold to be removed from the Authority's independence policy, in line with Parliament's repeated requests on the matter;
Amendment 8 #
Draft opinion Paragraph 7 c (new) 7 c. Recalls that the Authority already has the possibility to organise expert hearings to which they can invite any expert, regardless of any conflict of interest, to answer questions posed by a scientific panel without the expert having the right to participate in the panel's deliberations and drafting of the opinion;
Amendment 9 #
Draft opinion Paragraph 7 d (new) 7 d. Recalls that the revised Regulation (EC) No 178/20021a will require the Authority to pro-actively make regulatory data, that has been submitted by applicants, available to be downloaded, printed and searched through in an electronic format; whereas this will allow the Authority to benefit from extended peer review of the scientific community; recalls that this transparency requirement is indispensable for industry-sponsored research but it cannot be used as an argument to refuse academic data using data kept confidential for legitimate reasons, such as patients' personal medical records; _________________ 1aRegulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety (OJ L 031 1.2.2002, p. 1).
source: 641.159
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