Glossary:TAG-00328-Com-egu

Glossary > Compliance

Compliance
Tag-ID	TAG-00328-Com-egu
English	Compliance / Regulatory compliance / Adherence
French	Conformité / Conformité réglementaire / Respect des exigences
German	Compliance / Einhaltung / Regulatorische Konformität

References

	Scope	Document part	Language	Document
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 1 Part 2 6.	HM	Schedule 1 Part 2 6.	EN	GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004
ICH ICH E6 Guideline R3 (2025) Appendix B 12.3	G	Appendix B 12.3	EN	ICH ICH E6 Guideline R3 (2025)
ICH ICH E6 Guideline R3 (2025) Appendix B 2.5	G	Appendix B 2.5	EN	ICH ICH E6 Guideline R3 (2025)
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Compliance (in relation to trials)	G	GLOSSARY - Compliance (in relation to trials)	EN	ICH ICH E6 Guideline R3 (2025)
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.5	G	III. Annex 1 2.5	EN	ICH ICH E6 Guideline R3 (2025)
ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.12	G	III. Annex 1 3.12	EN	ICH ICH E6 Guideline R3 (2025)
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
USA 21 CFR Part 812 09-Apr-2025 § 812.110 (b)	MD	§ 812.110 (b)	EN	USA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.30 (b) - (c)	MD	§ 812.30 (b) - (c)	EN	USA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.46 (a)	MD	§ 812.46 (a)	EN	USA 21 CFR Part 812 09-Apr-2025
USA 45 CFR Part 46 09-Apr-2025 Subpart E	G	Subpart E	EN	USA 45 CFR Part 46 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