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DHRHealth Institute for Research and Development

Office of Human Research Protection Program

The Office of Human Research Protection Program (OHRPP) manages all clinical research conducted under the guidance of DHR Health Institute for Research & Development. OHRPP in partnership with the research community is responsible for ensuring the safety and welfare of participants in clinical trials conducted under the aegis of the DHR Health Institute for Research & Development.

The DHR Health Institute for Research and Development currently follows the AAHRPP Accreditation Standards as it prepares to apply for accreditation. Accreditation from the Association for the Accreditation of Human Research Protection Program (AAHRPP) demonstrates the excellence of a research program which provides the most comprehensive protections for research participants.

OHRPP also provides administrative support to the Institutional Review Board (IRB), DHR Health Institute for Research & Development. It is also involved in facilitating the submission of clinical protocols by physician-investigators, fellows, residents, students and staff in various service lines at DHR Health System.
OHRPP is also responsible for ensuring compliance with Federal Wide Assurance (FWA 0014304) provided by the DHR Health Institute for Research & Development to the Office of Human Research Protection, Department of Health & Human Services. Below are some resources for investigators interested in conducting clinical research at DHR Health Institute for Research & Development:

CITI Training Program Registration Guide

CITI Training Program Registration Guide

[pdf-embedder url='https://dhrresearch.org/wp-content/uploads/2023/03/1.CITI-Training-Program-Registration-Guide.pdf']
Is my study considered Human Subject Research?

Is my study considered Human Subject Research?

[pdf-embedder url='https://dhrresearch.org/wp-content/uploads/2023/03/2.Is-my-study-considered-Human-Subject-Research.pdf']
What Review does my Human subject Research fall under?

What Review does my Human subject Research fall under?

[pdf-embedder url='https://dhrresearch.org/wp-content/uploads/2023/03/3.What-Review-does-my-Human-Subject-Research-fall-under.pdf']
Process for new study submission for research collaborators

Process for new study submission for research collaborators

[pdf-embedder url='https://dhrresearch.org/wp-content/uploads/2023/03/4.Process-for-new-study-submiission-for-research-collaborators.pdf']
Process for Submitting Application to use a Humanitarian Use Device

Process for Submitting Application to use a Humanitarian Use Device

[pdf-embedder url='https://dhrresearch.org/wp-content/uploads/2023/03/7.Process-for-Submitting-Application-to-use-a-Humanitarian-Use-Device.pdf']
DHR Guide to Waiver of Informed Consent

DHR Guide to Waiver of Informed Consent

[pdf-embedder url='https://dhrresearch.org/wp-content/uploads/2023/03/8.DHR-HIRD_Guide-to-Waiver-of-Informed-Consent.pdf']
Credentialing Form for Non-DHR Partners, RMF Physicians and Medical Staff

Credentialing Form for Non-DHR Partners, RMF Physicians and Medical Staff

[pdf-embedder url='https://dhrresearch.org/wp-content/uploads/2023/03/9.Credentialing-Form-for-Non-DHR-Partners-RMF-Physicians-and-Medical-Staff-.pdf']
DHR Expedited Reviewer Calendar

DHR Expedited Reviewer Calendar

[pdf-embedder url='https://dhrresearch.org/wp-content/uploads/2023/03/12.DHR-HIRampD-Expedited-Reviewer-Calendar.pdf']
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