Informed-consent meaning

Consent by a person to undergo a medical procedure, participate in a clinical trial, or be counseled by a professional such as a social worker or lawyer, after receiving all material information regarding risks, benefits, and alternatives.
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Consent, normally written, to surgery, experimental treatment, etc., given as by a patient after having been informed of the potential medical risks.
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Consent by a person to undergo a medical procedure, participate in a clinical trial, or be counseled by a professional such as a social worker or lawyer, after receiving all material information regarding risks, benefits, and alternatives.
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See consent.
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