Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Sub-Investigator
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| Document information | |
|---|---|
| Reference | ICH ICH E6 Guideline R3 (2025) |
| Validity area | ICH |
| Scope(s) | HM |
| Document name | ICH E6 Guideline |
| Version / Revision | R3 (2025) |
| Status | Current |
| Document type | International guideline |
| Language(s) | EN |
| Description | GUIDELINE FOR GOOD CLINICAL PRACTICE |
| Official source | Official link |
| Restricted access | No |
| Submitted by | Florian Adragna |
| Contributors | |
| Reference Details | |
|---|---|
| Module | Module 2 — Unit 2.3.1 |
| Scope | G |
| Document part | GLOSSARY - Sub-Investigator |
| Language | EN |
| Original entry by | Florian Adragna |
| Contributors | |
| Tags | Sub-investigator, Definition, Investigator oversight |
Content
Sub-Investigator Any individual member of the clinical trial team designated and under the oversight of the investigator to perform significant trial-related procedures and/or to make important trial-related decisions (e.g., associates, residents, research fellows).
