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Reference:EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022 2.9: Difference between revisions

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Revision as of 17:29, 15 July 2026



Document information
Reference EU EMA/786433/2022

Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022

Validity area EU
Scope(s) G
Document name EMA/786433/2022

Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units

Version / Revision 15-Nov-2022
Status Current
Document type Official guideline
Language(s) EN
Description EMA/786433/2022

Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units

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


Reference Details
Module Module 3 — Unit 3.2.1
Scope G
Document part 2.9
Language EN
Original entry by Florian Adragna
Contributors
Tags Enrolment, Informed consent, Screening, Undue inducement
Comment Recruitment and consent: key considerations

Content

2.9. Recruitment and consent Points to consider: • Recruitment strategies. • Volunteer database. • Collection and verification of the trial participants medical history. • Contact with the trial participant’s primary physician/family doctor. • Procedures to prevent ‘over-volunteering’. • Routine screening procedure (including any counselling or procedures for handling reportable diseases e.g. for positive serology results). • Trial participant records. • Procedures taken to verify the identity of the trial participants. Procedures for payment. • Procedures for taking consent (including verification that trial participants have understood the information).