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Informed Consent

Date of Publication:

9/5/2019

Definition:

Patients have the right to any and all necessary information in nonclinical terms to make knowledgeable decisions on consent or refusal for treatments, or participation in clinical trials or other research investigations as applicable.  Such information is to include any and all complications, risks, benefits, ethical issues, and alternative treatments as may be available.

Source of Definition:

Medical Program Support For Detainee Operations

Related Glossary Terms:

Informed Consent

Last Updated: September 14, 2022
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