Institutional Review Board (IRB) Suppport for CCVR Investigators

In conjunction with the Center for Clinical and Translational Research, the CCVR offers administrative assistance for IRB protocol development, submission, and review. We are very pleased to have Lynn Podraza, Regulatory Knowledge and Support Coordinator, serve as the dedicated IRB specialist for CCVR faculty engaging in human studies and clinical trials.

For more information, contact Lynn Podraza. Telephone: 312-996-2102 Email: podrazal @