A printed, optical, or electronic document designed to record all of the protocol required information to be reported to the sponsor on each trial subject.
Source: ICH Guideline E6: Good Clinical Practice.
Glossary
Case report form (CRF)
Resources
Take advantage of the knowledge and best practices gained from more than 20 years of research, innovation and development for the health and life sciences sectors.
Glossary
The Life Sciences glossary with terminology, acronyms, for regulatory, quality, compliance, clinical trials, and pharmacovigilance software.
Found 371 Results
Page 1 of 2
Page 1 of 2
Page 1 of 2
Page 1 of 2