The European medical technology industry is calling on the EU to join the Medical Device Single Audit Program (MDSAP) as a full member

MedTech Europe and COCIR are calling on the European Union to seek full participation in the Single Audit Program for Medical Devices by becoming a member of the MDSAP Regulatory Authority Council (“full member”) and to allow the recognition of MDSAP certificates for the purposes of CE marking of medical devices and in vitro diagnostic medical devices.

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