Glossary:TAG-00342-Sit-der

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Site resources
Tag-ID	TAG-00342-Sit-der
English	Site resources / Site facilities / Site equipment / Site infrastructure / Site capacity / Investigational site facilities / Trial site equipment
French	Ressources du site / Équipements du site / Installations du site / Infrastructure du site / Capacités du site / Équipements du centre investigateur
German	Ressourcen der Prüfstelle / Ausstattung der Prüfstelle / Einrichtungen der Prüfstelle / Infrastruktur der Prüfstelle / Kapazitäten der Prüfstelle

References

	Scope	Document part	Language	Document
DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 3 3.9	NIS	Leitlinie 3 3.9	DE	DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018
EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022 2.5-001	G	2.5	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 Article 50	HM	Article 50	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 10.3	MD	10.3	EN	ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.7	HM	4.7	EN	WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995