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Authorization and Informed Consent for Treatment of a Minor Dear Parent/Guardian: Treatment of minors requires a team effort by USMC\'s medical care provider(s) and the minor\'s parent or guardian.
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Who needs authorization and informed?

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Authorization and informed forms are typically required by healthcare providers, medical researchers, and institutions involved in clinical trials or experimental procedures.
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Additionally, individuals who are granting permission for someone else to make decisions on their behalf may also need to fill out such forms.
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Authorization and informed consent is a process by which a patient or research participant voluntarily agrees to participate in a particular treatment or research study after being informed of the potential risks and benefits.
Authorization and informed consent forms are typically required to be signed by patients, research participants, or legal guardians if the participant is a minor.
Authorization and informed consent forms are typically filled out by the healthcare provider or research investigator and then presented to the patient or participant for review and signature.
The purpose of authorization and informed consent is to ensure that individuals have a thorough understanding of the risks, benefits, and alternatives to a particular treatment or study before agreeing to participate.
Authorization and informed consent forms typically include information about the nature of the treatment or study, potential risks and benefits, confidentiality measures, and the right to withdraw consent at any time.
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