MDCG 2023-3: Q&A on vigilance terms and concepts under MDR and IVDR

MDCG Guidance MDCG 2025-01 rev.2
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Summary

MDCG 2023-3 — Q&A on vigilance terms and concepts under MDR and IVDR

Revision: rev.2

This is a guidance document endorsed by the Medical Device Coordination Group (MDCG) under the EU Medical Device Regulation (MDR 2017/745) and/or In Vitro Diagnostic Regulation (IVDR 2017/746).

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Document Details

Document IDMDCG 2023-3
TypeMDCG Guidance
AuthorityMDCG
Publication Date2025-01
Revisionrev.2

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Quick Info

TypeMDCG Guidance
Published ByMDCG
Date2025-01

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