BETA

8 Amendments of Thomas ULMER related to 2009/0003(CNS)

Amendment 23 #
Proposal for a recommendation
Recital 7
(7) Evidence suggests that EU Member States are at different levels in the development and implementation of effective and comprehensive patient safety strategies. Therefore, this initiative intends to create a framework to stimulate policy development and future action in and between Member States to address the key patient safety issues confronting the EU. In accordance with Article 152 of the Treaty establishing the European Community, however, there must be no encroachment upon Member States' competences.
2009/03/02
Committee: ENVI
Amendment 25 #
Proposal for a recommendation
Recital 8
(8) Patients should be informed and empowered by involving them in the patient safety process; they should be informed of levels of safety and on how they can find accessible and comprehensible information on complaints and redress systems. The individual Member State shall, however, be competent for the type and method of compensation.
2009/03/02
Committee: ENVI
Amendment 26 #
Proposal for a recommendation
Recital 10
(10) Comparable and aggregate data should be collected at Community level to establish efficient and transparent patient safety programmes, structures and policies, and best practices should be disseminated among the Member States. These data should only be used for the purposes of patient safety with respect to the control of healthcare associated infections. To facilitate mutual learning, a common terminology for patient safety and common indicators need to be developed through cooperation between Member States and the European Commission, taking into account the work of relevant international organisations.
2009/03/02
Committee: ENVI
Amendment 38 #
Proposal for a recommendation
Part I – Chapter II – point 3
(3) Member States should establish or strengthen reporting and learning systems on adverse events that: (a) Provide adequate information on the extent, types and causes of errors, adverse events and near misses; (b) Encourage healthcare workers to actively report through the establishment of a reporting environment which is open and fair. This reporting should be differentiated from Member States' disciplinary systems and procedures for healthcare workers, and the legal issues surrounding the healthcare workers' liability should be clarified.deleted
2009/03/02
Committee: ENVI
Amendment 41 #
Proposal for a recommendation
Part I – Chapter II – point 5 – point c
(c) To gather and share comparable data and information on patient safety outcomes in terms of type and number at EU level to facilitate mutual learning and inform priority setting. The scale and cost of the data collection, and use of the data collected, should not be disproportionate to the expected benefits. The data should only be collected in order to achieve the objective of reducing treatment-related infections through common learning. It shall be the responsibility of the Member States alone to set priorities for possible follow-up action, as these issues relate to the organisation of healthcare systems.
2009/03/02
Committee: ENVI
Amendment 53 #
Proposal for a recommendation
Annex 1 – line 9 – column 2
Freedom for a patient from unnecessary harm or potential harm associated with healthcarAbsence of adverse events, where an adverse event is defined as a harmful incident due more to the treatment than to the illness. This adverse event may be avoidable or unavoidable.
2009/03/02
Committee: ENVI
Amendment 54 #
Proposal for a recommendation
Annex 1 – line 7 – column 2
Health professionals working in clinical wards/departmentthe corresponding sectors who act as a liaison between their wards/departmentsork sector and the Infection Prevention and Control Team. Infection control link staff help promote infection prevention and control in their wards/departmentsectors and give feedback to the Infection Prevention and Control Team.
2009/03/02
Committee: ENVI
Amendment 55 #
Proposal for a recommendation
Annex 2 – Chapter 1 – point 1 – point b a (new)
(ba) Accepting and facilitating the use of information and communication technology tools, such as electronic instructions for use, in order to improve the understanding of users of the medical products.
2009/03/02
Committee: ENVI