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JOB General Consent Form Scripting General Consent, Treatment and Release of Information Page 1 Beaumont Health does not discriminate on the basis of race, color, national origin, age, disability
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Who needs informed consent and authorization?

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Anyone participating in a research study or clinical trial.
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Patients undergoing medical treatments or procedures.
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Individuals receiving healthcare services or treatments.
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Informed consent is a process for getting permission before conducting a healthcare intervention on a person, while authorization is the act of giving someone permission or power to do something.
Healthcare practitioners, researchers, or organizations are required to file informed consent and authorization.
Fill out the necessary forms with the required information and ensure that the participant fully understands and agrees to the terms.
The purpose of informed consent and authorization is to protect participants' rights and ensure they are fully informed about the risks and benefits of the intervention.
Information such as the nature of the intervention, potential risks and benefits, alternative treatments, confidentiality, and the right to withdraw from the intervention.
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