Public Health Effectiveness of the FDA 510(k) Clearance Process : Balancing Patient Safety and Innovation: Workshop Report
Institute of Medicine, Board on Population Health and Public Health Practice, Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process, Theresa Wizemann
The Food and Drug Administration (FDA) is responsible for assuring that medical devices are safe and effective before they go on the market. As part of its assessment of FDA's premarket clearance process for medical devices, the IOM held a workshop June 14-15 to discuss how to best balance patient safety and technological innovation. This document summarizes the workshop.
کال:
2010
خپرونه:
1
خپرندویه اداره:
National Academies Press
ژبه:
english
صفحه:
140
ISBN 10:
0309158508
ISBN 13:
9780309158503
فایل:
PDF, 2.96 MB
IPFS:
,
english, 2010
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