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    EC Unveils Designating Authority’s Final Assessment Form Under MDR, IVDR

    The European Commission’s Medical Device Coordination Group (MDCG) on Thursday released a final assessment form for authorities designating conformity assessment bodies (CABs) and notified bodies (NBs) under the EU Medical Devices Regulation (MDR), which takes effect next May, and the In Vitro Diagnostic Regulation (IVDR), which takes effect in May 2022. The form includes space to describe the assessment carried out by the designating authority and whether all correctiv...