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Last Approval Date: Stanford Hospital and Clinics Name of Policy: Informed Consent for Procedures and Treatments Departments Affected: All Departments I. October 12, 2011-Page 1 of 8 PURPOSE: This

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What is informed consent - medical?

Informed consent - medical is a process where a patient is provided with all relevant information about a medical treatment or procedure, including its purpose, potential risks and benefits, alternatives, and the patient's right to refuse or withdraw consent.

Who is required to file informed consent - medical?

The healthcare provider or medical professional performing the treatment or procedure is responsible for obtaining and filing the informed consent - medical.

How to fill out informed consent - medical?

Informed consent - medical forms typically require the patient or their legal representative to read and understand the provided information, ask questions if necessary, and then sign the form to indicate their voluntary agreement and understanding.

What is the purpose of informed consent - medical?

The purpose of informed consent - medical is to ensure that patients are able to make informed decisions about their medical care, understanding the risks, benefits, and alternatives involved, and to protect their right to autonomy and self-determination in healthcare decisions.

What information must be reported on informed consent - medical?

Informed consent - medical forms should include information about the specific treatment or procedure, its purpose, potential risks and benefits, alternatives, confidentiality, the patient's right to refuse, and any additional information that may be relevant to the specific case.

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