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Home » EC’s Device Group Issues Guidance on High-Risk IVDs During Transition Period
EC’s Device Group Issues Guidance on High-Risk IVDs During Transition Period
The European Commission’s Medical Device Coordination Group issued guidance for devicemakers of high-risk Class D in vitro diagnostics on applications during the transition period for the EU Invitro Diagnostic Regulation (IVDR) which will go into effect on May 26, 2022.
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