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Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - case -report form (CRF): Difference between revisions

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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
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|RefDocPart=Glossary - case -report form (CRF)
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|comment=Definition of case report form (GCP/ICH)
|content=case -report form (CRF)
A document that is used to record data on each trial subject during the course of the trial, as defined by the protocol. The data should be collected by procedures which guarantee preservation, retention and retrieval of information and allow easy access for verification, audit and inspection.
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! colspan="2" class="gplx-infobox-header" | Reference Details
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! Module
| Module 4 β€” Unit 4.2.5
|-
! Scope
| HM
|-
! Document part
| Glossary - case -report form (CRF)
|-
! Language
| EN
|-
! Original entry by
| Florian Adragna
|-
! Contributors
|
|-
! Tags
| [[Glossary:TAG-00124-Cas-PrΓΌ|Case report form]], [[Glossary:TAG-00244-Def-ini|Definition]], [[Glossary:TAG-00033-Pro-oto|Protocol]]
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| Definition of case report form (GCP/ICH)
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== Content ==
case -report form (CRF)
A document that is used to record data on each trial subject during the course of the trial, as defined by the protocol. The data should be collected by procedures which guarantee preservation, retention and retrieval of information and allow easy access for verification, audit and inspection.

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 β€” Unit 4.2.5
Scope HM
Document part Glossary - case -report form (CRF)
Language EN
Original entry by Florian Adragna
Contributors
Tags Case report form, Definition, Protocol

Content

case -report form (CRF) A document that is used to record data on each trial subject during the course of the trial, as defined by the protocol. The data should be collected by procedures which guarantee preservation, retention and retrieval of information and allow easy access for verification, audit and inspection.

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