Manufacturers hoping the U.S. Food and Drug Administration (FDA) might adopt a more European-style approach to device approval got a strongly negative signal in a May agency report. Includes the full text of U.S. FDA Report on Devices Approved in the EU but Not in the U.S.
EU-Style Device Approval Poses Patient Safety Risks, U.S. FDA Says
- Post author:Sam
- Post published:April 7, 2016
- Post category:International Medical Device Regulatory Monitor