Office of the Vice President for Research - Research Administration
Office of Clinical Research
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Thursday, February 23, 2017
11:00 a.m. - 12:00 p.m.
Long Campus, Med Room 311C
Preparation for AAHRPP Site Visit
Investigator’s Role for Meeting Human Research Protection Standards
Learn More about Forums
Get Ready for the AAHRPP Site Visit
Updates to OCR Forms & Policies
As of June 8, 2016:
new policy: Quality Assurance and Improvement Program
Make sure to always download forms from the OCR and IRB websites to ensure you are using the most current versions!
The OCR is committed to supporting the research community in the conduct of ethical clinical research and human subject protection in compliance with the required federal, state, and local regulations. The office provides consultation on questions related to regulations and standards of practice governing human research. The OCR provides education and training; develops policy and processes; and leads quality improvement efforts in areas of clinical trial management. It endeavors to create an interdisciplinary collaborative environment among the research teams, fostering best practices.