Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 10.7 (e): Difference between revisions
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| | | [[Glossary:TAG-00292-Eme-ent|Emergency unblinding]], [[Glossary:TAG-00123-Bli-ppe|Blinding]], [[Glossary:TAG-00031-Pat-onA|Patient information sheet]], [[Glossary:TAG-00201-Cli-eSt|Clinical investigation]] | ||
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Revision as of 17:29, 15 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 3 — Unit 3.3.1 |
| Scope | MD |
| Document part | 10.7
(e) |
| Language | EN |
| Original entry by | Florian Adragna |
| Contributors | |
| Tags | Emergency unblinding, Blinding, Patient information sheet, Clinical investigation |
| Comment | Subject information on emergency procedures related to trial |
Content
[...] e) provide the subject with [...]