The regulatory division of the Office of Clinical Trials Research has been established to handle both the regulatory needs for the institution as well as provide support for individual investigators needs. The regulatory division can provide assistance in IRB submissions, VCC/PRC submissions and GCRC submissions as well as sponsor regulatory document submissions.
Office of Clinical Trials Research
UHC Campus, Arnold 3436
All clinical trial agreements, confidentiality agreements, and amendments requiring institutional sign-off by our institution official will be reviewed by the Office of Clinical Trials Research prior to signature.
Please send contracts and amendments to Mark Tomase at the Office of Clinical Trials Research.
Last modified November 13 2015 09:35 AM