Institutional review Board (IRB)
About the board
The University of Akron Institutional Review Board for the Protection of Human Subjects (IRB) is an administrative body established to protect the rights and welfare of individuals recruited for participation in research conducted under the auspices of the university or its affiliates. Its mission is to advance an organizational culture and infrastructure that supports the highest ethical standards in the review and implementation of research with human participants. The University of Akron gives the IRB ultimate authority for approval of research with human participants.
- University of Akron IRB Guidelines
- IRB Forms
- Federal Regulations and Guidance
State of Ohio mandates which impacting “human” (e.g., behavioral or physiological) face-to-face research were lifted as of June 2, 2021. However, the following campus protocols are still in place for your own personal safety and the safety of others while on campus.
The University encourages anyone who is not fully vaccinated, feeling ill or who is immunocompromised to use caution and consider facial coverings for their personal safety.
Masks continue to be required at some campus locations. (See Coronavirus info, scroll down and open Mask Policy.)
The University continues to monitor conditions and guidance from the Centers for Disease Control, the State of Ohio and Summit County Public Health and adjusts masking and other protocols as needed.
Masks must be made available to human research subjects meeting with researchers in-person on campus. Social distancing is not required. Researchers are urged to accommodate a research subject’s request for social distancing while on campus if possible.
It is recommended to clean and disinfect all surfaces touched by multiple people (such as door handles, tables, shared equipment, shared keyboards) between each person’s use.
Wash hands or use hand sanitizer frequently.
If feeling sick, reschedule your in-person on campus meeting for a different date/time or meet virtually.
If you have questions, please email email@example.com and include your IRB number (if you have an active protocol), or call Jandy Hanna, Research Compliance Officer, Office of Research Administration at 330-972-4394.
IRB applications must be submitted electronically, via email to firstname.lastname@example.org.
- Full board review protocols (those greater than minimal risk or not within a category eligible for exemption or expedited review) may take 2-3 months from initial review to approval.
- Some IRB applications can be approved through exempt or expedited review procedures. These applications do not generally require a presentation to the full board.
- IRB applications eligible for exempt or expedited review may be submitted electronically any time and will be reviewed as they are received.
- The process for exempt and expedited review and approval takes about two to four weeks. Expect an additional 2-4 weeks review period if revisions or updates are required.
- IRB registrations for determination that the project is not human subjects research may be reviewed in 1-2 weeks.
- Expect an additional 1-2 weeks review period if clarifications are requested.
In general, the more complete the initial proposal, the less time it takes for approval. Applicants should retain a copy of their protocol for their own records. For questions, please contact the Office of Research Administration, 330-972-4394 or email@example.com.
IRB MEETING SCHEDULE AND APPLICATION DATE
IRB meetings are held as needed during the fall and spring semesters. If needed, additional meeting(s) are scheduled. Applications, which require full board review, are due approximately one month prior to the IRB Meeting.
|Month||Meeting Date (application due ~ one month prior)|
|September 2023||Tuesday, September 12, 12pm-1pm|
|October 2023||Wednesday, October 11, 11am-1pm|
|November 2023||Monday, November 13, 12pm-2pm|
|December 2023||Monday, December 11, 10am-12pm|