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Home » MDCG Releases Guidance About ‘Authorized Representatives’
MDCG Releases Guidance About ‘Authorized Representatives’
The EU’s Medical Device Coordination Group (MDCG) has released new guidance on requirements created by the Medical Device Regulation (MDR) and In Vitro Diagnostic Medical Device Regulation (IVDR) for devicemakers’ “authorized representatives,” including who, when and how to register.