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Reference:EU EMA/INS/GCP/143492/2022 - ANNEX I TO PROCEDURE FOR CONDUCTING GCP INSPECTIONS REQUESTED BY THE CHMP: INVESTIGATOR SITE 2022 Page 6

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Document information
Reference EU EMA/INS/GCP/143492/2022

- ANNEX I TO PROCEDURE FOR CONDUCTING GCP INSPECTIONS REQUESTED BY THE CHMP: INVESTIGATOR SITE 2022

Validity area EU
Scope(s) G
Document name EMA/INS/GCP/143492/2022

- ANNEX I TO PROCEDURE FOR CONDUCTING GCP INSPECTIONS REQUESTED BY THE CHMP: INVESTIGATOR SITE

Version / Revision 2022
Status Current
Document type Official guideline
Language(s) EN
Description EMA/INS/GCP/143492/2022

Good Clinical Practice Inspectors Working Group (GCP IWG)

ANNEX I TO PROCEDURE FOR CONDUCTING GCP INSPECTIONS REQUESTED BY THE CHMP: INVESTIGATOR SITE

Official source Official link
Restricted access No
Submitted by Florian Adragna
Contributors


Reference Details
Module Module 3 — Unit 3.1.1
Scope G
Document part Page 6
Language EN
Original entry by Florian Adragna
Contributors
Tags Consent process, Documentation, Source documents, Assent, Informed consent

Content

[…] Documentation in the source data of the process of obtaining the initial informed consent and subsequent consent to updates, including paediatric assent and emergency consent, if applicable. […]