ARTICLE
19 March 2015

FDA Releases Report On National Medical Device Surveillance System

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The report reflects recent studies by FDA examining the effectiveness of its postmarket oversight systems.
United States Food, Drugs, Healthcare, Life Sciences

In the February 25, 2015, Federal Register, FDA announced the availability of the report titled Strengthening Patient Care: Building an Effective National Medical Device Surveillance System, developed by the National Medical Device Postmarket Surveillance System Planning Board. The report reflects recent studies by FDA examining the effectiveness of its postmarket oversight systems. FDA is soliciting comments from stakeholders. Comments due April 27, 2015.

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