Search

Informed consent

Author:
WWARN

Freely-given informed consent obtained from every participant prior to their clinical trial participation is one of the principles of ICH GCP. This procedure describes how informed consent may be obtained from competent adults for clinical trials with a template information and consent form for a typical malaria efficacy trial (for adaptation).

Informed consent

zip
13 April 2018
Informed consent
2.0
zip
726.12 KB