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Clinical research / Pharmaceutical industry / Medical ethics / Design of experiments / Human subject research / Clinical trial / Office for Human Research Protections / Food and Drug Administration / Public Responsibility in Medicine and Research / Clinical research coordinator


See Does My Project Need IRB Review? If there is any question whether your project is human subject research you must submit this form to the IRB. Complete all sections then email to . Th
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Document Date: 2016-01-27 16:54:35


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