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.
12/15/2020
In an effort to improve efficiency, the UC Human Research Protection Program (HRPP) is rolling out a new process to collect and report financial relationships related to study sponsors. HRPP has developed a new fillable PDF financial disclosure form that can easily be completed and signed using electronic signature. Read the full announcement for more information.
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.
11/29/2018
See the full announcement for more details on what is needed and how to apply.
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.
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
11/01/2018
FEE INCREASE for Externally Funded Studies
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
Effective January 18, 2017 more studies require registration in clinicaltrials.gov and the reporting requirements have increased.
Human Research Protection Program (ML0567) University of Cincinnati University Hall, Suite 300 P.O. Box 210567 Cincinnati, OH 45221-0567
University Hall, Suite 300 51 Goodman Drive Cincinnati, OH 45221-0567
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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