Informed Consent and Refusal: A Guide to the Fundamentals

Informed consent (IC) is a two-way educational and communication process intended to prevent patients from being treated without their permission and understanding.

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By asking questions and obtaining information about proposed treatments or interventions - especially invasive procedures carrying some possibility of harm - patients become aware of potential benefits, risks and alternatives prior to authorizing care. The IC process is a legal and ethical obligation, serving to enhance decision-making and protect both parties. Read More

Resources

Informed Consent, from the American Medical Association.
Informed Consent, from the National Telehealth Policy Resource Center.
Informed Consent FAQs, from the Office of Human Research Protections, U.S. Department of Health & Human Services.

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