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

{{ReferenceData
|has_document=Document:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
|module=4
|unit=4.2.5
|scope=HM
|doc_part=Glossary - case -report form (CRF)
|language=EN
|entry_by=Florian Adragna
|contributors=
|tags=TAG-00124-Cas-Prü ++ TAG-00244-Def-ini ++ TAG-00033-Pro-oto
|tags_display=[[Glossary:TAG-00124-Cas-Prü|Case report form]], [[Glossary:TAG-00244-Def-ini|Definition]], [[Glossary:TAG-00033-Pro-oto|Protocol]]
|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.
}}