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SUN DOWNSTATE MEDICAL CENTER UNIVERSITY HOSPITAL OF BROOKLYN POLICY AND PROCEDURE No: RAD 20A Page Subject:INFORMED CONSENTOriginal Issue Date:12/2009Prepared by: James ShanahanSupersedes:12/2009Reviewed
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RAD-20A informed consent.docx is a document used to obtain formal consent from individuals participating in research or clinical studies, ensuring they are aware of the nature of the study and any potential risks involved.
Researchers, academic institutions, or organizations conducting studies that require informed consent from participants are required to file the RAD-20A informed consent document.
To fill out the RAD-20A informed consent.docx, individuals must provide participant details, description of the study, risks involved, benefits, and signature lines for both the participant and the researcher.
The purpose of the RAD-20A informed consent.docx is to ensure that participants are fully informed about the study and voluntarily agree to participate, protecting their rights and well-being.
The RAD-20A informed consent.docx must report participant information, study objectives, procedures, risks, benefits, confidentiality provisions, and contact information for questions.
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