Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A A.17: Difference between revisions
From GxPlex
Migrate to Template:ReferenceData for PageForms (GxPlexBot) |
Gxplex admin (talk | contribs) m 1 revision imported |
(No difference)
| |
Latest revision as of 13:50, 16 July 2026
| Document information | |
|---|---|
| Reference | ISO ISO 14155 -
Clinical investigation of medical devices for human subjects 2020 |
| Validity area | ISO |
| Scope(s) | MD |
| Document name | ISO 14155 -
Clinical investigation of medical devices for human subjects |
| Version / Revision | 2020 |
| Status | Current |
| Document type | International guideline |
| Language(s) | EN |
| Description | ISO 14155:2020
Clinical investigation of medical devices for human subjects — Good clinical practice |
| Official source | Official link |
| Restricted access | Yes |
| Submitted by | Florian Adragna |
| Contributors | |
| Reference Details | |
|---|---|
| Module | Module 6 — Unit 6.5.0 |
| Scope | MD |
| Document part | Annex A
A.17 |
| Language | EN |
| Original entry by | Florian Adragna |
| Contributors | |
| Tags | Publication, ClinicalTrials.gov, Investigation plan, Clinical investigation |
Content
A.17 Publication policy […]
