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July 10, 2018
Next Social Behavioral IRB meeting
July 12, 2018
Next Biomedical IRB meeting
Research in the News
Check out various news items related to human subjects research here.
New Forms Introduced
On March 14, new versions of all our submission forms were introduced. Effective March 28, current versions of IRB forms (version dated, 03/14/2018) will be required for all new submissions. New submissions on previous versions of IRB 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.
Delays in Common Rule Revisions
The revisions to the Common Rule have been delayed until January of 2019.
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.
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.