Office of the Vice President for Research - Research Administration
Trial Sponsor's, CRO's and External Investigators, Contact us as you look to place your clinical trial.
Accredited since 2009
OCR Concierge Services
OCR Support & Regulatory Guidance
|March 22, 2017
|April 4, 2017
|April 5, 2017
|April 19, 2017
|May 2, 2017
|May 3, 2017
|May 17, 2017
|May 31, 2017
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Office of Clinical Research
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Thursday, May 18, 2017
3:00 p.m. – 4:00 p.m.
Long Campus, Med Room 309L
FDA Submissions – What Is The Process?
& Velos eResearch Training
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Get Ready for the AAHRPP Site Visit
Updates to OCR Website, Forms, Policies
As of March 20, 2017:
new content: External IRB Prompt Reporting and External IRB Inactivations/Progress Report
updated Scope of Practice form
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.