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Medical Device CRO Blog

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IRB Reporting Compliance - Whose Job is it?

Posted by Sandra Maddock on Wed, Nov 07, 2012 @ 07:25 AM

Recently, when discussing Institutional Review Board (IRB) adverse event reporting, a Project Manager for a leading medical device Contract Research Organization (CRO) brought up a valuable question regarding reporting compliance- whose job is it to ensure an investigator is compliant with IRB reporting policies?

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