IMDRF/GRRP WG/N59 FINAL:2024 (Edition 2): Requirements for Regulatory Authority Recognition of Conformity Assessment Bodies Conducting Medical Device Regulatory Reviews
Summary
Final Technical document
This document has been developed by the International Medical Device Regulators Forum (IMDRF) — a voluntary group of medical device regulators from around the world who work together to accelerate international convergence in medical device regulation.
Document Details
- Document Code: IMDRF/GRRP WG/N59 FINAL:2024 (Edition 2)
- Type: Technical document
- Issuing Authority: IMDRF
- Date: 2024-04-26
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Source: International Medical Device Regulators Forum (IMDRF). This content is provided for informational purposes. Always refer to the official IMDRF document for the most current version.