IMDRF/NCAR WG/N14 FINAL:2025 (Edition 5): Medical Devices: Post-Market Surveillance: National Competent Authority Report Exchange Criteria and Report Form
Summary
Information 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/NCAR WG/N14 FINAL:2025 (Edition 5)
- Type: Information document
- Issuing Authority: IMDRF
- Date: 2025-04-01
Access the Full Document
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.
Document Details
Document IDIMDRF/NCAR WG/N14 FINAL:2025 (Edition 5)
TypeIMDRF Information document
AuthorityIMDRF
Publication Date2025-04-01