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Section 5. Informed Consent This section provides information on informed consent procedures for MTN016. Sites may choose to enroll each woman infant pair using a single consent form; alternatively,
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Read through the informed consent form carefully, paying attention to the V20 version.
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Provide personal information, such as your full name, date of birth, and contact details.
03
Understand the purpose and nature of the study or procedure for which you are giving your consent.
04
Review any potential risks or benefits associated with participating in the study or procedure.
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Make sure to ask any questions or seek clarification for any concerns before signing the consent form.
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If applicable, have a witness sign the form as well to validate the process.
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Who Needs Informed Consent V20:

01
Individuals who are planning to participate in a research study.
02
Patients undergoing medical procedures that require informed consent.
03
Participants in clinical trials or experimental treatments.
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