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August 9, 2016
Next Social Behavioral IRB meeting
August 11, 2016
Next Biomedical IRB meeting
Submissions are pre-reviewed by OPRS before IRB review. Items requiring full board review must be determined to be ready, with pre-review issues resolved, no less than two weeks prior to the meeting date. This allows adequate processing time and ensures sufficient review time for the IRB members.
We are excited to launch the new OPRS web-site and hope the additional guidance and resources will help our research community. We welcome any thoughts or comments you may have regarding the site. Provide feedback.
All research involving human subjects that is conducted at or sponsored by the University of Illinois at Urbana-Champaign, whether funded or unfunded and whether conducted by Illinois faculty or others, must comply with applicable policies for the protection of human subjects.
Getting started with the IRB
I'm a researcher, what should I know?
What should I know before becoming a research participant?
The Office for the Protection of Research Subjects (OPRS), while performing administrative functions of the Institutional Review Board (IRB), serves as the official oversight office for human subject research at Illinois. The office is the central point of contact for investigators, research subjects, and regulatory agencies. OPRS organizes and documents the IRB review process, monitors research regulations, produces educational resources for faculty and staff, and provides assurance that the Urbana campus is in compliance with federal, state, and campus policies. Contact OPRS.