Glossary:TAG-00124-Cas-Prü

Glossary > Case report form

Case report form
Tag-ID	TAG-00124-Cas-Prü
English	Case report form / Electronic case report form
EN Abbr.	CRF / eCRF
French	Cahier d'observation / Cahier d'observation électronique
FR Abbr.	CO / eCO
German	Prüfbogen / Elektronischer Prüfbogen / Beobachtungsbogen
DE Abbr.	CRF / eCRF

References

	Scope	Document part	Language	Document
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Case Report Form (CRF)	G	GLOSSARY - Case Report Form (CRF)	EN	ICH ICH E6 Guideline R3 (2025)
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.12.5 – 2.12.9	G	III. Annex 1 2.12.5 – 2.12.9	EN	ICH ICH E6 Guideline R3 (2025)
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 6.6	MD	6.6	EN	ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020
USA 21 CFR Part 312 09-Apr-2025 § 312.62 (b)	HM	§ 312.62 (b)	EN	USA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 314 09-Apr-2025 § 314.50	HM	§ 314.50	EN	USA 21 CFR Part 314 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.140 (a) (3)	MD	§ 812.140 (a) (3)	EN	USA 21 CFR Part 812 09-Apr-2025
USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025 Page 3 - CRF	G	Page 3 - CRF	EN	USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025
USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025 Page 3 - Note	G	Page 3 - Note	EN	USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025
WHO WHO - Guidance for best practices for clinical trials 2024 2.1.8	G	2.1.8	EN	WHO WHO - Guidance for best practices for clinical trials 2024
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - case -report form (CRF)	HM	Glossary - case -report form (CRF)	EN	WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995