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consent to clinical research  

Definition

  • Informed consent practices have evolved over time after instances were documented in which research participants were not treated fairly or respectfully, were not informed, or were subjected to unnecessary harm. Current federal regulations support the ethical treatment of persons in the research setting in that the participation is voluntary, that the risks outweigh the benefits, and that all people are given an equal chance to participate. [Source: Encyclopedia of Psychology and Law; Consent to Clinical Research]

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https://concepts.sagepub.com/social-science/concept/consent_to_clinical_research

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