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Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - monitor: Difference between revisions

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{{#set:
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|HasDocument=Document:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
|has_document=Document:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
|RefScope=HM
|module=4
|RefDocPart=Glossary - monitor
|unit=4.3.1
|RefLanguage=EN
|scope=HM
|RefTags=TAG-00020-Cli-nit ++ TAG-00244-Def-ini ++ TAG-00137-Mon-che ++ TAG-00017-Spo-die ++ TAG-00148-Con-rsc
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|entry_by=Florian Adragna
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|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
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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.
}}
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{{:Document:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995}}
{| class="wikitable gplx-infobox"
|-
! colspan="2" class="gplx-infobox-header" | Reference Details
|-
! Module
| Module 4 — Unit 4.3.1
|-
! Scope
| HM
|-
! Document part
| Glossary - monitor
|-
! Language
| EN
|-
! Original entry by
| Florian Adragna
|-
! Contributors
|
|-
! Tags
| [[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
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== 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.

Revision as of 12:56, 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.

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