Human Research Protection Program

The Human Research Protection Program provides training and support for research involving human subjects including Institutional Review Board (IRB) protocols and FDA submissions and supports the IRB.

  • 21st Annual Human Subject Protection Conference

    07/16/2019

    This year’s conference will address issues of critical importance to human subject protections. See full announcement for registration information and further details.

    Full Announcment >
  • Board Members Needed to Help Review Human Subject Research

    11/29/2018

    See the full announcement for more details on what is needed and how to apply.

    Full Announcment >
  • New Electronic System

    11/29/2018

    The IRB electronic protocol system is changing to facilitate research and comply with new regulations. The shift out of ePAS and into RAP (Research Administrative Portal) will occur in January of 2019. All research submissions must be in an approved state for IT to move them over into the new system. To facilitate the migration of the data and prevent delays, researchers are strongly encouraged to send any new research submissions (i.e., new studies, amendments, continuing reviews, reportable events) by December 7, 2018. Submissions that are not in an approved state at the time of migration must be re-entered and submitted in the new system.

    Full Announcment >
  • User Survey

    11/07/2018

    The University of Cincinnati Human Research Protection Program (HRPP) and Institutional Review Board (IRB) are moving to a new electronic system and would like you to fill out a survey to collect a snapshot of your personal experience. Click "See Full Announcement" for more information

    Full Announcment >
  • New IRB Review Fees Effective January 1, 2019

    11/01/2018

    FEE INCREASE for Externally Funded Studies

    Full Announcment >
  • Exempt Study Amendments

    04/19/2018

    Amendments are only necessary for exempt studies when the proposed modification are substantive or change the study procedure such that the study no longer qualifies for exempt review

    Full Announcment >
  • Clinicaltrials.gov

    04/19/2018

    Effective January 18, 2017 more studies require registration in clinicaltrials.gov and the reporting requirements have increased.

    Full Announcment >

Contact

Mailing Address

Human Research Protection Program (ML0567)
University of Cincinnati
University Hall, Suite 300
P.O. Box 210567
Cincinnati, OH 45221-0567

Street Address

University Hall, Suite 300
51 Goodman Drive
Cincinnati, OH 45221-0567

View on map

General Inquiries

Phone: 513-558-5259

Email: irb@ucmail.uc.edu

To report compliance concerns: Email: research.compliance@uc.edu or Call - 513-558-5034

Toll-Free Anonymous Compliance Hotline - (800) 889-1547

You may also file a report via the web: Anonymous Online Reporting