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C. PARTICIPANT INFORMED CONSENT FOR HIV TESTING TEMPLATEProtocol No. Protocol Title. Subject No: Name of Investigator: Dear Participants part of the above research study, you are being asked to undergo
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Participant informed consent is obtained to ensure that individuals are fully aware of the risks and benefits of participating in a research study before they agree to take part.
Researchers conducting a study involving human subjects are required to obtain and file participant informed consent.
Participant informed consent forms should be filled out by providing all relevant information about the study, risks, benefits, and participant rights in a clear and understandable manner.
The purpose of participant informed consent is to protect the rights and welfare of research participants by ensuring they have all necessary information to make an informed decision about participating.
Participant informed consent forms should include information about the study purpose, procedures, risks, benefits, confidentiality, voluntariness, and contact information for questions.
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