Glossary:TAG-00037-End-ung

Glossary > Trial end

Trial end
Tag-ID	TAG-00037-End-ung
English	End of a clinical trial / Trial completion / Last patient last visit
French	Fin d'un essai clinique / Fin de l'étude / Dernier patient dernière visite
German	Ende einer klinischen Prüfung / Prüfungsende / Studienende

References

	Scope	Document part	Language	Document
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 77 Paragraph 4 – 5	MD	Article 77 Paragraph 4 – 5	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 5	IVD	Article 73 Paragraph 5	EN	EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 77 Paragraph 4 – 5	IVD	Article 77 Paragraph 4 – 5	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 37 Paragraph 1 – 7	HM	Article 37 Paragraph 1 – 7	EN	EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 37 Paragraph 4	HM	Article 37 Paragraph 4	EN	EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022
GBR Directive 2001/20/EC 04-Apr-2001 Article 10 (c)	HM	Article 10 (c)	EN	GBR Directive 2001/20/EC 04-Apr-2001
GBR The Medical Devices Regulations 2002 11-Feb-2021 Article 16 (11)	MD	Article 16 (11)	EN	GBR The Medical Devices Regulations 2002 11-Feb-2021
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 27	HM	Article 27	EN	GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 3 Part 1 1. (p)	HM	Schedule 3 Part 1 1. (p)	EN	GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004