Submit your IRB Application in a Fast, Easy & Efficient way with our AI Assistant to get your IRB Approval Quickly.
Institutional Review Board Committee for the Protection of Human Subjects at Gannon University is the established authority assigned to review research proposals in which humans are the subjects of research.
Policies established by the Department of Health and Human Services (HHS) in the Code of Federal Regulations require that Institutional Review Boards (IRB) be established to review and act on all research proposals involving human subjects at colleges and universities to safeguard and protect human subjects' health, well-being, and rights. Gannon University's special identity recognizes the dignity and sacredness of all human beings and thus endorses such safeguards and protection.
All research proposals that include the use of human subjects for research whether conducted by faculty or students should be reviewed by the IRB. Research proposals that include the use of non-human animals with backbones whether conducted by faculty or students should be reviewed by the IACUC. Research proposals that do not use humans or other animals with backbones as subjects are not reviewed by either IRB or IACUC.
Second and last Tuesday of the month during the fall and spring semester.
10 Submitted all year round
10 working days to meeting.
IRB meets to discuss Standard Reviews on the last Tuesday of the month that Gannon University. Due to spring break and Easter holidays, spring meetings may take place on the second to last Tuesday. Standard Reviews must be submitted at least 10 working days prior to the meeting. Non-standard reviews may be submitted throughout the year. More information here.
IRB Committee Members
Click the Video Link to watch a brief tutorial.
Standard
A standard (full committee review) application is required if: Research involves greater than minimal risk OR Target population is a federally protected group
Expedited
An expedited application should be submitted if a study involves less than minimal risk, does not target a federally protected population, and meets one of the expedited categories.
Exempt
An exempt application should be submitted if a study involves less than minimal risk, does not target a federally protected population, and meets one of the exempt categories.
Required Application Attachments
Find the documents are required to be attached (if applicable to your study).
Register your institution or get in touch to learn more about the IRB System
If you don't see an answer to your question, you can send us an email from our contact form
This depends on whether or not the project meets the criteria of human subject research. To determine whether an IRB is needed, please complete the "How to determine if your project requires IRB approval" form above under the "Other Resources" tab.
Your Gannon network ID is the first part of your Gannon University e-mail address (all the characters before the "@").
The following attachments are required (if applicable to your study):
1. Citi training certificate for all investigators and faculty advisor
2. Informed consent
3. Any recruitment material (e.g., flyer, e-mail scripts, etc.)
4. Outcome measures (e.g., survey, interview questions, etc.)
Save all documents into a folder and then compress or zip the folder. Then attach the zipped/compressed folder to the application.
When completing your IRB application, input the name and Gannon e-mail address of the faculty member advising your research study. When you application is completed, your faculty advisor will need to log into their IRB account and approve your application. Once your advisor approves the application, log into your IRB account and click on "submit" application.
***Your application will not be submitted until your faculty advisor approves your application
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