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Title Location Functional Area Informed Consent and Authorization in Research ALL Beaumont Health Research Institute Policy Owner Document Type Effective Date Administrative Director Policy 10/21/2016
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Who needs informed consent and authorization?

01
Any individual who wishes to participate in a research study or medical procedure may need to provide informed consent and authorization.
02
Patients undergoing medical treatments or procedures often require informed consent and authorization.
03
Participants in clinical trials, scientific research, or surveys may need to provide informed consent and authorization.
04
Minors or individuals lacking decision-making capacity usually require consent from their legal guardian or representative.
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Informed consent is when a person agrees to allow something to happen, such as a medical procedure, with full knowledge of all the facts. Authorization is the act of giving someone permission to do something.
Individuals receiving medical treatment or participating in research studies are required to provide informed consent and authorization.
To fill out informed consent and authorization, individuals must carefully read and understand all information provided, ask any questions they may have, and then sign the document to indicate their agreement.
The purpose of informed consent and authorization is to ensure that individuals are fully informed about their medical treatment or participation in research studies and to protect their rights.
Informed consent and authorization forms typically include information about the treatment or study being conducted, potential risks and benefits, alternatives, and the individual's rights.
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