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The process whereby people are given the key facts about a clinical trial before deciding whether or not to participate. This is a continuing process throughout the study to provide further information for participants. Informed consent is not a contract, and the participant may withdraw from the trial at any time.
See also:
Clinical trial
Eligibility criteria
Drop out
Trial endpoint
Informed consent document
Bias, Committee for Medicinal Products for Human Use (CHMP), Quality of life trials, Clinical trial, Defined daily dose (DDD), Drug-drug interaction, Randomised trial, Responsiveness, Treatment Investigational New Drug (IND), Toxicity, Recruitment status, Pharmacokinetics, Methodology, Baseline, Field experiments,
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