All research protocols involving human subjects must be reviewed and approved by the UIC Institutional Review Board (IRB) prior to initiating the study. We provide:
- consultation on all types of IRB submissions
- preliminary review of IRB application documents
- assistance with drafting specific documents
For questions or assistance, contact Sandra Rahbe, Regulatory Support Coordinator, at firstname.lastname@example.org.
Assistance with submissions is provided in the order that they are received. Because of the complex nature of IRB applications, next day review cannot be accommodated.