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Medical research / Medical ethics / Research / Health / Autonomy / Clinical research ethics / Food and Drug Administration / Informed consent / Expanded access / Investigational New Drug / Consent / Clinical trial


Instructions Questions? Contact the IRB Education Specialist atSee guidance GUI-6 and HRPP Policy Manual Chapter 5.9. Report to IRB The protocol director must submit the following to the IRB within five (
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Document Date: 2016-04-12 01:21:50


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