Glossary:TAG-00083-Enr-enr

Glossary > Enrolment

Enrolment
Tag-ID	TAG-00083-Enr-enr
English	Enrolment / Recruitment / Patient enrolment
French	Inclusion / Recrutement / Recrutement des patients
German	Einschluss / Rekrutierung / Patientenrekrutierung / Patienteneinschluss

References

	Scope	Document part	Language	Document
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40 Absatz 2	G	§ 40 Absatz 2	DE	DEU AMG - Arzneimittelgesetz 19-Jul-2023
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 33 Absatz 2	MD	§ 33 Absatz 2	DE	DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022
EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022 2.9	G	2.9	EN	EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX I Section K No. 59-60	HM	ANNEX I Section K No. 59-60	EN	EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.2	G	III. Annex 1 2.2	EN	ICH ICH E6 Guideline R3 (2025)
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 3.42 - recruitment	MD	3.42 - recruitment	EN	ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020
USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023 II. Advertising-001	G	II. Advertising	EN	USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023
USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023 II. Advertising-002	G	II. Advertising	EN	USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.3	HM	4.3	EN	WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995