Institutional Review Board
The use of human subjects in research is extremely important to the development of new knowledge in many areas. However, careful attention must be given to questions of ethics and human dignity whenever human subjects participate in research.
All research involving human subjects (including course projects, capstone projects, master’s theses, and independent student research) must be formally reviewed and approved before any data are collected.
Types of Applications
Research protocols should be submitted to Mail Stop PAC 525, Attention: Office of Research & Sponsored Programs or email@example.com. The level of review required for each protocol (exempt, expedited, or full IRB review) will be determined by the UIS Human Subjects Review Officer.
Unless a waiver is requested, subjects must be informed before they can consent to participate in the research.
Please plan for 1-2 weeks for HSRO review, and 4-6 weeks for full board review.
All investigators involved with the collection and/or analysis of human subjects research must complete training before the project can begin. The training is free for members of the UIS community and can be completed online, following the instructions on our Required Training page.
Please be advised that we accept protocols on a rolling basis, but the deadline date for protocol submissions that may require full Board approval is two weeks prior to the scheduled IRB monthly meeting.
The Fall 2019 meeting schedule and protocol submission deadlines are posted below. All meetings will be held in PAC 457.
|Fall 2019 Meeting Dates||Time||Deadline date for protocol submission|
|Sept. 17, 2019||11:00AM – 1:00 PM||Sept. 3, 2019|
|Oct. 24, 2019||11:00AM – 1:00 PM||Oct. 10, 2019|
|Nov. 21, 2019||11:00AM – 1:00 PM||Nov. 7, 2019|
IRB Did You Know…?
how to apply for an anonymous online survey
or getting an Exempt Protocol approved in 15 easy steps At UIS, anonymous online surveys qualify for Exempt status. The application form is on the Forms, Templates, and Checklists tab of Institutional Review Board page. A video describing the procedure for applying for an Exempt protocol is now loaded onto the Resources and Training page […]
what are the new categories of Exempt research
As described in the prior post, the revised Federal Common Rule includes many burden-reducing changes. The amended regulations revise and clarify the categories of research that are exempt from full board review. There are eight categories of exemptions, which expand on the prior six categories. If the research involves pregnant women, fetuses, neonates, prisoners, or […]
For additional explanation and instructions please view the Introduction to the IRB Presentation (PDF). Further training materials are available in the IRB section of the Resources page. Note that the new EU General Data Protection Regulation may apply to your research. Please consult the University of Illinois system GDPR Information page, which contains a section for Researchers.
UIS’ IRB is authorized by a Federalwide Assurance for the Protection of Human Subjects, #FWA00013968, through 12/13/2021. Our Human Research Protections Policy is available on our Policy page.