Glossary:TAG-00203-Cli-lin

Glossary > Investigation plan

Investigation plan
Tag-ID	TAG-00203-Cli-lin
English	Clinical investigation plan / Clinical investigation protocol
EN Abbr.	CIP
French	Plan d'investigation clinique / Protocole d'investigation clinique
German	Klinischer Prüfplan / Klinisches Prüfprotokoll

References

	Scope	Document part	Language	Document
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex XV Chapter I Section 2	MD	Annex XV Chapter I Section 2	EN	EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023
GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021 2.-001	MD	2.	EN	GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021
GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021 2.-002	MD	2.	EN	GBR Clinical investigations of medical devices – compiling a submission to MHRA May 2021
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 10.6	MD	10.6	EN	ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 6.1	MD	6.1	EN	ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020
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
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A - CIP	MD	Annex A - CIP	EN	ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020
USA 21 CFR Part 812 09-Apr-2025 § 812.25	MD	§ 812.25	EN	USA 21 CFR Part 812 09-Apr-2025
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.4 - Introduction	HM	4.4 - Introduction	EN	WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995