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December 11, 2018
Next Social Behavioral IRB meeting
December 13, 2018
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.
Revisions to the Common Rule
On December 3, new versions of our Protocol and Exempt Forms were updated to be compliant with the revisions to the Common Rule. Beginning January 9, 2019, current versions of the Protocol and Exempt Forms (version dated, 12/03/2018) will be required for all new submissions. New submissions on previous versions of the Protocol or Exempt Forms will be returned to the PI with instructions to resubmit on current forms. All applications must be type written and signed by the PI. New forms can be accessed here.
Illinois is now a member of SmartIRB, an online reliance system to aid in collaborative agreements across campuses.
Research in the News
Check out various news items related to human subjects research here.
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.
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.