IRB Committee 1
IRB Committee 1 is responsible for the full review of human subjects research protocols submitted by faculty/staff for:
- Health & Human Performance (HHP) Department of CLASS
- College of Education
- College of Medicine
- College of Natural Sciences & Mathematics
- College of Nursing
- College of Optometry
- College of Pharmacy
- College of Technology
- Cullen College of Engineering
Full Committee
Submission Deadlines | IRB 1 Meeting Dates |
Friday, August 7, 2020 | Friday, August 21, 2020 |
Friday, September 4, 2020 | Friday, September 18, 2020 |
Friday, October 2, 2020 | Friday, October 16, 2020 |
Friday, November 6, 2020 | Friday, November 20, 2020 |
Wednesday, November 25, 2020 | Friday, December 11, 2020 |
Friday, January 8, 2021 | Friday, January 22, 2021 |
Friday, February 5, 2021 | Friday, February 19, 2021 |
Friday, February 26, 2021 | Friday, March 12, 2021 |
Friday, April 2, 2021 | Friday, April 16, 2021 |
Friday, May 7, 2021 | Friday, May 21, 2021 |
Friday, June 4, 2021 | Friday, June 18, 2021 |
Friday, July 2, 2021 | Friday, July 16, 2021 |
Friday, August 6, 2021 | Friday, August 20, 2021 |
*Dates are subject to change without notice if circumstances require rescheduling.
Expedited Review
Protocols falling under an expedited category and involving no more than minimal risk, as well as minor changes in approved full board protocols, may be reviewed under an expedited process. The Chair of IRB 1 either reviews or delegates the review to one or more experienced IRB members, who review the protocol under applicable regulations and either approve or require modifications to the protocol prior to approval. An expedited reviewer may not disapprove a protocol, but may forward to the fully convened committee for further determination if warranted. Expedited submissions are considered on a rolling basis, thus turnaround time for these submissions is expected to be quicker than for protocols undergoing full board review.
Exempt Status
Protocols falling under an exempt category defined under the federal regulations require administrative review by the IRB office to ensure that basic ethical principles, such as confidentiality of data and obtaining informed consent where applicable, are addressed. Applications for exempt protocols are reviewed by IRB staff on a rolling basis, thus turnaround time for these submissions is expected to be quicker than for protocols undergoing full board review.