Important Note: As of April 1, 2014, the IRB will NOT accept applications from students. Faculty members supervising students must sign and submit the IRB application on the student's behalf. Applications, modifications, amendments, continuing reviews, termination/completion reports, etc. submitted by students will not be processed by the IRB.
The CSU Institutional Review Board (IRB) reviews research protocols involving the use of human subjects.* No research project involving human subjects can begin until written authorization is received by the investigator from the CSU IRB. Deadline dates for IRB submissions are indicated on the Meeting Schedule link.
Three types of review can be requested depending on the type of study. These are as follows:
- Exempted (Administrative) Review
- Expedited Review
- Full Committee Review
The type of review will depend on the nature of the proposed research. Descriptions of criteria for exempt and expedited review are contained in the "Application for Initial Review", accessed through the "Forms" link. Researchers should indicate which type of review they are requesting; the final determination is made by the IRB.
Please note: If the proposed research involves more than minimal risk to the potential subjects or involves a vulnerable class of persons under the federal code, the project does not qualify for exempt review. If the protocol involves collecting audiotape or videotaped data sets, the project does not qualify for exempt review. Finally, if the protocol involves minors, prisoners, pregnant women, handicapped or mentally disabled persons, it is the policy of the CSU IRB to require a full committee review.
The following definitions from the Federal Code should be use to determine whether your project must be submitted to the IRB for review.
"Any living individual(s) about whom an investigator (whether professional or student) conducting research obtains (1) data through interaction or intervention with the individual, or (2) identifiable private information."
45 CFR 46 §102 (f)
"Any systematic investigation, including research development, testing, evaluation, designed to develop or contribute to generalizable knowledge."
45 CFR 46 §102 (d)Any data collection activity from human subjects, including surveys,interviews, focus groups, assessments or evaluations, that is designed to contribute to generalized knowledge requires IRB review. The definition of generalized knowledge is broad, and includes theses, dissertations, publications, or public presentations. If you are uncertain if your proposed research falls within the categories listed above, please contact the IRB at (773) 995-5078 or email@example.com for assistance.
For all research and research-related activities involving human subjects, please download the "Application for Initial Review" under the "Forms" link at left. This document also contains a set of application instructions, and an "Investigator Agreement" form. Please submit an electronic copy of your application (PDF is preferred) to: firstname.lastname@example.org. In addition, please submit a signed hard copy of your application to the IRB office in Cook Administration Building 304A. Submission of both an electronic and hard copy application is needed before the Institutional Review Board can review your application. Once a study has been assigned a protocol #, please use this # in the subject line of all email correspondences with the IRB. If you have questions concerning the submission process or the status of your application please contact Daniel Gibboney Jr, IRB coordinator, at email@example.com or at (773) 995-5405.
Please allow AT LEAST two weeks for review and notification. Written notification will be sent by email to the prinicipal investigator. As noted, final approval must be received before initiating the research study.
Please note that the above specified timelines for protocol approval are contingent upon completion and receipt of all protocol application materials including initial application form, investigator agreement, consent forms, completion certificates, surveys, tests, and advertisements (where applicable), approval notices from outside institutions (where applicable) and letters of access from agencies or institutions other than Chicago State University.