IMDRF document
IMDRF/MC/N1FINAL:2022 (Edition 5)
IMDRF Procedural document · IMDRF/MC/N1FINAL:2022 (Edition 5) · posted Dec 19, 2022
Key facts
| Title | IMDRF/MC/N1FINAL:2022 (Edition 5) |
|---|---|
| Document reference | IMDRF/MC/N1FINAL:2022 (Edition 5) |
| Issued by | IMDRF |
| Document category | Procedural document |
| Posted | Dec 19, 2022 |
| IMDRF page | imdrf.org |
| Document file | live-imdrf.pantheonsite.io |
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About IMDRF and GHTF documents
IMDRF is a forum of medical device regulators that writes harmonised guidance, such as the MDSAP audit documents and the UDI, SaMD and adverse-event terminology documents. It also hosts the archived documents of its predecessor, the Global Harmonization Task Force (GHTF).
Source: International Medical Device Regulators Forum (IMDRF), including the archived documents of the Global Harmonization Task Force (GHTF) · Source date: