Reference:IMDRF IMDRF โ Guidelines - -: Difference between revisions
From GxPlex
gxplex>GxPlexBot Import from GxPlex Excel |
Gxplex admin (talk | contribs) m 1 revision imported ย |
||
| (4 intermediate revisions by 4 users not shown) | |||
| Line 1: | Line 1: | ||
{{ | {{ReferenceData | ||
| | |has_document=Document:IMDRF IMDRF โ Guidelines - | ||
| | |module=4 | ||
| | |unit=4.5.1 | ||
| | |scope=MD | ||
| | |doc_part=- | ||
| | |language=EN | ||
| | |entry_by=Florian Adragna | ||
|contributors= | |||
ย | |tags=TAG-00113-Aud-tQu ++ TAG-00155-Med-Med ++ TAG-00218-Har-pรคi | ||
|tags_display=[[Glossary:TAG-00113-Aud-tQu|Audit]], [[Glossary:TAG-00155-Med-Med|Medical device]], [[Glossary:TAG-00218-Har-pรคi|Harmonised standard]] | |||
ย | |comment=IMDRF/GHTF: international medical device regulatory standards | ||
|content=IMDRF: International Medical Device Regulators Forum ; Global Harmonization Task Force (GHTF) | |||
|- | |||
|- | |||
|- | |||
| ย | |||
| | |||
| | |||
ย | |||
= | |||
IMDRF: International Medical Device Regulators Forum ; Global Harmonization Task Force (GHTF) | |||
GHTF Study Group 4 โ Auditing | GHTF Study Group 4 โ Auditing | ||
| Line 50: | Line 17: | ||
No final document (01-Feb-2024), but archived documents available. | No final document (01-Feb-2024), but archived documents available. | ||
}} | |||
Latest revision as of 13:50, 16 July 2026
| Document information | |
|---|---|
| Reference | IMDRF IMDRF โ Guidelines - |
| Validity area | IMDRF |
| Scope(s) | MD |
| Document name | IMDRF โ 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 | |
| Reference Details | |
|---|---|
| Module | Module 4 โ Unit 4.5.1 |
| Scope | MD |
| Document part | - |
| Language | EN |
| Original entry by | Florian Adragna |
| Contributors | |
| Tags | Audit, Medical device, Harmonised standard |
Content
IMDRF: International Medical Device Regulators Forum ; Global Harmonization Task Force (GHTF) GHTF Study Group 4 โ Auditing
https://www.imdrf.org/documents/ghtf-final-documents/ghtf-study-group-4-auditing
No final document (01-Feb-2024), but archived documents available.
