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Key Sources For EU MDR Post-Market Surveillance

Europe's Medical Device Regulation (MDR) post-market surveillance requirements have been applicable since May 26, 2021, for all medical devices. ....

Leeanne Baker , European Commission , Medical Devices Regulation , Vitro Diagnostic Medical Devices Regulation , Notified Bodies , From Users And Patients , Including Posts On Social , Risk Data , Notified Body , Press Corner ,