An Institutional Review Board (IRB) is an appropriately constituted group that has been formally designated to review and monitor research involving human subjects. An IRB has the authority to approve, require modifications in (to secure approval), or disapprove research. This review serves an important role in the protection of the rights and welfare of human research subjects.
The purpose of IRB review is to assure, both in advance and by periodic review, that group appropriate steps are taken to protect the rights and welfare of humans participating in the research. To accomplish this purpose, IRBs use a group process to review research protocols and related materials (e.g., informed consent documents and protocols) ensure protection of the rights and welfare of human subjects.
To access ePAS - click on link below, or copy and paste into browser: https://epas.research.cchmc.org/ePAS_PRD
U.C. and affiliated sites, login by clicking on the U.C. logo at the
bottom of the page. You will then login using your U.C. credentials.
For study specific questions, please contact the IRB Office member responsible for your department using the following link: Departmental Dedication - find your IRB representative
For ePAS specific questions or to set up ePAS training, please contact Claudia Norman, 558-5784.
Click here to identify the person dedicated to serving your research group
Angela Braggs-Brown, RAC, CIP, MA
Kareemah Mills, CIP
Claudia Norman, CIP
Sr. Regulatory Compliance Specialist
558-5784 email@example.com Human Protection Administrators
Jo Ann Behrle
558-6915 firstname.lastname@example.org Quality Assurance Auditors
Jackie Glass, CCRP
Tammy Stiver, CCRP
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