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Healthcare Glossary
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Informed consent document
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
Related terms
Data Protection Act, Effectiveness, Fair balance, Inclusion/exclusion criteria, Drug-drug interaction, Phase II trials, Interventions - clinical, New product development (NPD), Controlled trial, Cohort, Risk-benefit analysis, ABPI Code of Practice, Treatment Investigational New Drug (IND), Prescription only medicine (POM), Placebo-controlled trial,
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