Informed consent
A suggested process for how informed consent may be obtained from competent adults in a typical antimalarial clinical trial
Publication Version
2.0
Publication Code
AD06
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).