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Facility:NYC Health+Hospitals Kings CountyINFORMED CONSENT FOR INVASIVE, DIAGNOSTIC, MEDICAL & SURGICAL PROCEDURESChart No. Name Unit (Patient Imprint Card)FORM B1 I hereby permit ___ (Name of Attending
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Who needs rethinking informed consent form?

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Researchers conducting studies or experiments involving human subjects.
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Healthcare providers obtaining consent for medical procedures or treatments.
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Legal professionals when seeking consent for legal matters.
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Anyone involved in activities that require informed consent to ensure transparency and protection of individuals' rights.
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The rethinking informed consent form is a document that outlines the details of a research study, including the risks and benefits involved, and allows the participant to make an informed decision about participation.
Researchers conducting a study are required to provide participants with a rethinking informed consent form.
The rethinking informed consent form is typically filled out by the participant, after reviewing the information provided by the researcher.
The purpose of the rethinking informed consent form is to ensure that participants understand the risks and benefits of participating in a research study and can make an informed decision.
The rethinking informed consent form must include details about the study, risks and benefits, participant rights, and contact information for the researcher.
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