Device developers must take action as experts leave FDA
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Device developers must take action as experts leave FDA
A former FDA reviewer offers advice to help innovative medtech avoid new and more dangerous pitfalls. By Naomi Schwartz, Medcrypt The FDA’s Center for Devices and Radiological Health (CDRH) is experiencing significant workforce shortages that will affect the timely review of medical devices submitted to the FDA for review in 2025, particularly in areas requiring… The post Device developers must take action as experts leave FDA appeared first on …
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