How the new European regulation on medical devices will affect innovation

被引：32

作者：

Ben-Menahem, Shiko M. ^{[1
]}

Nistor-Gallo, Raymond ^{[2
]}

Macia, Gloria ^{[3
]}

von Krogh, Georg ^{[1
]}

Goldhahn, Joerg ^{[4
]}

机构：

[1] Swiss Fed Inst Technol, Dept Management Technol & Econ, Zurich, Switzerland

[2] QMD Serv GmbH, Vienna, Austria

[3] F Hoffmann La Roche & Cie AG, Basel, Switzerland

[4] Swiss Fed Inst Technol, Dept Hlth Sci & Technol, Zurich, Switzerland

来源：

NATURE BIOMEDICAL ENGINEERING | 2020年 / 4卷 / 06期

关键词：

D O I：

10.1038/s41551-020-0541-x

中图分类号：

R318 [生物医学工程];

学科分类号：

0831 ;

摘要：

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

引用

页码：585 / 590

页数：6

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