Glossary:TAG-00038-Ear-tig

Glossary > Early termination

Early termination
Tag-ID	TAG-00038-Ear-tig
English	Early termination of a clinical trial / Premature termination / Early stop
French	Arrêt anticipé d'un essai clinique / Arrêt prématuré de l'essai / Terminaison anticipée de l'essai
German	Abbruch einer klinischen Prüfung / Vorzeitiger Abbruch / Frühzeitiger Studienabbruch

References

	Scope	Document part	Language	Document
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77	MD	Article 77	EN	EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 Paragraph 1 – 3	MD	Article 77 Paragraph 1 – 3	EN	EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 Paragraph 1, 3 & 4	MD	Article 77 Paragraph 1, 3 & 4	EN	EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 73 Paragraph 1, 3, 4	IVD	Article 73 Paragraph 1, 3, 4	EN	EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 26 - 29	HM	Article 2 Paragraph 26 - 29	EN	EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 38	HM	Article 38	EN	EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022
GBR Directive 93/42/EEC 11-Oct-2007 Article 15 6. - 7.-001	MD	Article 15 6. - 7.	EN	GBR Directive 93/42/EEC 11-Oct-2007
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 31	HM	Article 31	EN	GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.6	G	III. Annex 1 2.6	EN	ICH ICH E6 Guideline R3 (2025)
ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.17.1	G	III. Annex 1 3.17.1	EN	ICH ICH E6 Guideline R3 (2025)
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 8.2	MD	8.2	EN	ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020
USA 21 CFR Part 312 09-Apr-2025 § 312.44	HM	§ 312.44	EN	USA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 312 09-Apr-2025 § 312.44 (d)	HM	§ 312.44 (d)	EN	USA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 312 09-Apr-2025 § 312.56	HM	§ 312.56	EN	USA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.3 (q)	MD	§ 812.3 (q)	EN	USA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.46 (b) - (c)-002	MD	§ 812.46 (b) - (c)	EN	USA 21 CFR Part 812 09-Apr-2025
USA 45 CFR Part 46 09-Apr-2025 § 46.123	G	§ 46.123	EN	USA 45 CFR Part 46 09-Apr-2025
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.15	HM	4.15	EN	WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 5.14	HM	5.14	EN	WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995