How the new European regulation on medical devices will affect innovation

The European Union’s new regulatory framework for medical devices has central implications for the development of new devices, particularly by start-ups.

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Bibliographische Detailangaben
Veröffentlicht in:	Nature biomedical engineering 2020-06, Vol.4 (6), p.585-590
Hauptverfasser:	Ben-Menahem, Shiko M., Nistor-Gallo, Raymond, Macia, Gloria, von Krogh, Georg, Goldhahn, Jörg
Format:	Artikel
Sprache:	eng
Schlagworte:	639/166/985 692/700/565 706/648/453 706/703/166/988 706/703/66 Biomedical and Life Sciences Biomedical Engineering/Biotechnology Biomedicine Comment Diagnostic Equipment - standards Equipment and Supplies - standards Equipment Safety European Union Health Care Sector - standards Humans Medical equipment Medical innovations Patient Safety Policy Making Social Control, Formal
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Beschreibung
Zusammenfassung:	The European Union’s new regulatory framework for medical devices has central implications for the development of new devices, particularly by start-ups.
ISSN:	2157-846X 2157-846X
DOI:	10.1038/s41551-020-0541-x