Improved clinical investigation and evaluation of high-risk medical devices: the rationale and objectives of CORE-MD (Coordinating Research and Evidence for Medical Devices)

Abstract In the European Union (EU) the delivery of health services is a national responsibility but there are concerted actions between member states to protect public health. Approval of pharmaceutical products is the responsibility of the European Medicines Agency, whereas authorizing the placing...

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Veröffentlicht in:	European heart journal. Quality of care & clinical outcomes 2022-05, Vol.8 (3), p.249-258
Hauptverfasser:	Fraser, A G, Nelissen, R G H H, Kjærsgaard-Andersen, P, Szymański, P, Melvin, T, Piscoi, P
Format:	Artikel
Sprache:	eng
Schlagworte:	Cardiology Europe European Union Hospitals Humans Medical device industry Medical equipment Medical technology Orthopedics Public health Regulation Regulatory agencies Review
Online-Zugang:	Volltext
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