Property:RefUnit
From GxPlex
Unit number this reference belongs to.
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 1 Part 2 7 +
2.4.0 +
E
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 +
2.4.0 +
U
USA FDA Guidance for Industry Investigator Responsibilities — Protecting the Rights, Safety, and Welfare of Study Subjects Oct-2009 III. B. +
2.4.0 +
I
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - informed consent +
3.1.1 +
3.1.1 +
C
CIOMS CIOMS - International Ethical Guidelines for Biomedical Research Involving Human Subjects 2016 Page 23 +
3.1.1 +
I
E
