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A document which describes the rights of participants in a clinical study, as well as explaining details of the study. This includes the study’s purpose, duration, required procedures, and key contacts, while also outlining the risks and potential benefit.
See also:
Clinical trial
Eligibility criteria
Drop out
Trial endpoint
Prevention trials, Phase I trials, Dose-ranging trial, Big pharma, Compassionate use, Treatment Investigational New Drug (IND), Phase III trials, Recruiting, Screening trials, Clinical trial, Over the counter (OTC), Meta analysis, Committee for Medicinal Products for Human Use (CHMP), Defined daily dose (DDD), Controlled trial,
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