Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - monitor: Difference between revisions
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{{ | {{ReferenceData | ||
| | |has_document=Document:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 | ||
| | |module=4 | ||
| | |unit=4.3.1 | ||
| | |scope=HM | ||
| | |doc_part=Glossary - monitor | ||
| | |language=EN | ||
| | |entry_by=Florian Adragna | ||
|contributors= | |||
|tags=TAG-00020-Cli-nit ++ TAG-00244-Def-ini ++ TAG-00137-Mon-che ++ TAG-00017-Spo-die ++ TAG-00148-Con-rsc | |||
|tags_display=[[Glossary:TAG-00020-Cli-nit|CRA / Monitor]], [[Glossary:TAG-00244-Def-ini|Definition]], [[Glossary:TAG-00137-Mon-che|Monitoring]], [[Glossary:TAG-00017-Spo-die|Sponsor]], [[Glossary:TAG-00148-Con-rsc|CRO]] | |||
|comment=Definition of monitor | |||
|content=monitor | |||
A person appointed by, and responsible to, the sponsor or Contract Research Organization (CRO) for the monitoring and reporting of progress of the trial and for verification of data. | |||
}} | }} | ||
Latest revision as of 13:50, 16 July 2026
| Document information | |
|---|---|
| Reference | WHO WHO - Guidelines for GCP for trials on
pharmaceutical products* 1995 |
| Validity area | WHO |
| Scope(s) | HM |
| Document name | WHO - Guidelines for GCP for trials on
pharmaceutical products* |
| Version / Revision | 1995 |
| Status | Current |
| Document type | International guideline |
| Language(s) | EN |
| Description | World Health Organization
WHO Technical Report Series, No. 850, 1995, Annex 3 Guidelines for good clinical practice (GCP) for trials on pharmaceutical products* |
| Official source | Official link |
| Restricted access | No |
| Submitted by | Florian Adragna |
| Contributors | |
| Reference Details | |
|---|---|
| Module | Module 4 — Unit 4.3.1 |
| Scope | HM |
| Document part | Glossary - monitor |
| Language | EN |
| Original entry by | Florian Adragna |
| Contributors | |
| Tags | CRA / Monitor, Definition, Monitoring, Sponsor, CRO |
Content
monitor A person appointed by, and responsible to, the sponsor or Contract Research Organization (CRO) for the monitoring and reporting of progress of the trial and for verification of data.
