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On April 17, the Food and Drug Administration's Center for Devices and Radiological Health (CDRH) issued its 2024 safety report. As an update to their 2018 Medical Device Safety Action Plan...
New guidance to advance medical device safety, regulatory oversight, and innovation On April 17, the Food and Drug Administration's Center for Devices and Radiological Health ...
This guidance describes FDA’s participation in the Voluntary Improvement Program (VIP). The VIP is a voluntary program intended to guide improvement to enhance the quality of devices.
The FDA seeks comments on its proposed guidance describing its policy regarding FDA's participation in the Voluntary Improvement Program. The...
The FDA seeks comments on its proposed guidance describing its policy regarding FDA's participation in the Voluntary Improvement Program. The...