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Informed Consent Guidebook P 1 of 68 VAM HCS HUMAN RESEARCH PROTECTION GUIDANCE HIP 03.01G Approval date: 3/11/11 Version: 3.0 RESEARCH INFORMED CONSENT GUIDEBOOK (HIP 03.01G) Veteran Affairs Maryland
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What is informed consent overview?
Informed consent overview is a document that explains the study or procedure to be done, the risks and benefits involved, and the participant's rights.
Who is required to file informed consent overview?
Researchers, doctors, or medical professionals conducting studies or procedures involving human subjects are required to file informed consent overview.
How to fill out informed consent overview?
Informed consent overview is typically filled out by providing detailed information about the study or procedure, explaining risks and benefits, and obtaining the participant's signature.
What is the purpose of informed consent overview?
The purpose of informed consent overview is to ensure that participants are fully informed about the study or procedure they are participating in, and to protect their rights as research subjects.
What information must be reported on informed consent overview?
Informed consent overview must include details about the study or procedure, risks and benefits, confidentiality, voluntary participation, and contact information for questions.
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