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See OHRS Information Sheet Outside Interest Disclosure for guidance on submission requirements. DFCI IRB and the DFCI Office of Research Integrity ORI. I agree to report to the sponsor IRB FDA OHRP NIH all site-responsible investigators and any other required sponsor or agency the adverse experiences that occur in the course of the investigation s. If any required training is incomplete or expired this submission will be returned and/or disapproved. If Human Subject Protection training will...
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