Document:IMDRF IMDRF – Guidelines -: Difference between revisions
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Latest revision as of 14:15, 16 July 2026
| Document information | |
|---|---|
| Reference | IMDRF IMDRF – Guidelines - |
| Validity area | IMDRF |
| Scope(s) | MD |
| Document name | IMDRF – Guidelines |
| Version / Revision | - |
| Status | N.A. |
| Document type | Corpus of texts |
| Language(s) | EN |
| Description | IMDRF: International Medical Device Regulators Forum
IMDRF documents - https://www.imdrf.org/documents/library - Technical documents Global Harmonization Task Force (GHTF) - https://www.imdrf.org/documents/ghtf-final-documents GHTF Study Group 1 - Pre-market Evaluation GHTF Study Group 2 - Post-market Surveillance/Vigilance GHTF Study Group 3 - Quality Systems GHTF Study Group 4 - Auditing GHTF Study Group 5 - Clinical Safety/Performance |
| Official source | Official link |
| Restricted access | No |
| Submitted by | Florian Adragna |
| Contributors | |
References
| Scope | Document part | Language | Preview | |
|---|---|---|---|---|
| IMDRF IMDRF – Guidelines - - | MD | - | EN | IMDRF: International Medical Device Regulators Forum ; Global Harmonization Task Force (GHTF)
GHTF Study Group 4 – Auditing https://www.imdrf.org/doc… |
