Reference:EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022 2.5-002: Difference between revisions
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| | | [[Glossary:TAG-00018-Inv-die|Investigator]], [[Glossary:TAG-00017-Spo-die|Sponsor]], [[Glossary:TAG-00340-Req-nfo|Requirements]] | ||
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Revision as of 17:29, 15 July 2026
| Document information | |
|---|---|
| Reference | EU EMA/786433/2022
Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022 |
| Validity area | EU |
| Scope(s) | G |
| Document name | EMA/786433/2022
Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units |
| Version / Revision | 15-Nov-2022 |
| Status | Current |
| Document type | Official guideline |
| Language(s) | EN |
| Description | EMA/786433/2022
Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units |
| Official source | Official link |
| Restricted access | No |
| Submitted by | Florian Adragna |
| Contributors | |
| Reference Details | |
|---|---|
| Module | Module 4 — Unit 4.5.2 |
| Scope | G |
| Document part | 2.5 |
| Language | EN |
| Original entry by | Florian Adragna |
| Contributors | |
| Tags | Investigator, Sponsor, Requirements |
| Comment | Repeated entry: 4.5.2 ++ 2.4.0
Personnel requirements: investigator-sponsor relationship |
Content
2.5. Personnel Points to consider: […] • Relationship of the Investigator with the Sponsor company. […]
