IMDRF document
Non-In Vitro Diagnostic Device Market Authorization Table of Contents (nIVD MA ToC)
IMDRF Technical document · IMDRF/RPS WG/N9FINAL:2019 (Edition 3) · posted Mar 21, 2019
Key facts
| Title | Non-In Vitro Diagnostic Device Market Authorization Table of Contents (nIVD MA ToC) |
|---|---|
| Document reference | IMDRF/RPS WG/N9FINAL:2019 (Edition 3) |
| Issued by | IMDRF |
| Document category | Technical document |
| Posted | Mar 21, 2019 |
| IMDRF page | imdrf.org |
| Document file | imdrf.org |
At a glance
- Yes Full text searchable in Orca1
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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: