Human Research Protections Office (HRPO)

Naval Medical Center Portsmouth is the IRB of Record for DDEAMC.  EIRB system is required for all submissions.  CITI training should be IAW the DHA guidelines (affiliate with the Office of the Under Secretary of Defense for Personnel and Readiness (OUSD(P&R), in the CITI Program, and complete the associated Human Subjects Research Training appropriate for their research role). All projects being reviewed by NMCP IRB require all investigators to complete the Responsible Conduct of Research (RCR) modules in CITI training in addition to training that is specific to the type of research being conducted.​

Investigator Forms can be found on IKEnet under the DCQS/ Human Research Protections Office(HRPO) site. If submitting an Informed Consent Form (ICF) please use the template on the HRPO site, NMCP template (ICF and HIPAA together) and attach this document in EIRB under the ICF section for submission.
Research Funding/SOW/Budget POC:
Externally funded research requires review by the DDEAMC Department of Clinical Investigations
Chief, Department of Clinical Investigation (DCI)


Contact Us


Chief, HRPO/Human Protections and Compliance Administrator (HPA)

Protocol Coordinator

Senior Compliance Specialist & EIRB Administrator

Research Consults POC

Department of Clinical Investigation


Mon. - Fri. 7:30 a.m. - 4 p.m.


Bldg 38711
Fort Eisenhower, GA 30905

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