By Mehryar Behizad2023-12-05T16:00:00
Richard Vincins outlined how post-market surveillance (PMS) is becoming increasingly important around the world in many jurisdictions. Previously, PMS activities used to be concentrated on vigilance and complaints, however the Medical Device Regulation (MDR) explicitly identifies sources of data which have not previously been properly identified or evaluated. Even if these are identified, the evaluation and analysis of their data was lacking in detail and methodology.
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