Human Subjects		The IRB at UNH: Responsibilities (cont.)				13 of 14
Introduction Case Study Brief History Ethical Principles & Key Issues The IRB at UNH Case Study Review			Assure that research personnel under their supervision are adequately trained and act in an ethical manner Provide a copy of the IRB-approved, signed informed consent document to each subject at the time of consent (unless the IRB has specifically waived this requirement) Forward to the IRB any proposed modification(s) prior to initiation; changes must not be initiated prior to receipt of written approval without contingencies from the IRB
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