If you have any questions pertaining to the policies, please contact the IRB Coordinator.
Links to applicable guidance documents, policies, forms, and websites can be found in the footnotes of the PH IRB Policy & Procedures Manual.
Children Participation in Research
Prisoner Participation in Research
Protocol Deviations and Noncompliance
Responding to Allegations of Research Misconduct
Unanticipated Problems and Adverse Events
Compensating Research Participants
Financial Conflicts of Interest in Federally Sponsored Research
Transportation of Information Assets
The PH IRB does not have the clinical expertise to review research protocols involving the criteria discussed in the below listed policies. PHD policies have been developed for these studies, however, the Division directs the PH IRB to cede oversight on such requests to a commercial or central IRB knowledgable in such research and the FDA regulations with which they must comply.
Research involving Investigational Medical Devices
Treatment Use of an Investigational New Drug (IND)
Emergency Use of an Investigational Drug
Emergency Research - Exception to Informed Consent