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CDRH Seeks To Expand Public-Private Medical Device Epidemiology Network

This article was originally published in The Gray Sheet

Executive Summary

FDA hopes the MDEpiNet post-market surveillance program will be fully functional by the end of the year. A May public meeting is planned to catalyze the effort.

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CDRH Officials Talk New Guidance, Post-Market Surveillance And 510(k)s At AdvaMed

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