How the new European regulation on medical devices will affect innovation

被引:0
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作者
Shiko M. Ben-Menahem
Raymond Nistor-Gallo
Gloria Macia
Georg von Krogh
Jörg Goldhahn
机构
[1] ETH Zürich,Department of Management, Technology and Economics
[2] QMD Services GmbH,Department of Health Sciences and Technology
[3] F. Hoffmann-La Roche AG,undefined
[4] ETH Zürich,undefined
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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.
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页码:585 / 590
页数:5
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