IRB Policies & Forms
Â鶹ÊÓƵ's Institutional Review Board Policy
On Sept. 20, 2018, Â鶹ÊÓƵ's Board of Regents approved the new IRB policy which governs human subjects research at Â鶹ÊÓƵ. You can download the policy below.
IRB Required Training
You must have completed CITI training on human subject protection within the past three years to submit an application to the Â鶹ÊÓƵ IRB. Your certificate of completion is required as part of the IRB application. Other training opportunities must be approved by the IRB to be considered as a replacement. If you are a Â鶹ÊÓƵ employee, please follow these instructions to register and complete the CITI training.
If you are a Â鶹ÊÓƵ student and would like to enroll in our free online course, log in to Blackboard via the MyÂ鶹ÊÓƵ portal. Go to Organizations. Click on Organization Catalog in the upper, right-hand corner. Choose ID in the first drop-down menu. In the box, type irb_training. When the IRB_Training appears in the list, click on the down arrow next to the organization ID. Click on Enroll. You will have to have a copy of an approved training certificate of completion from within the past three years to submit with your IRB application.
IRB Application Forms
Other IRB Forms
- Research Sponsor Form
- Research Protocol Modification Form
- Annual Progress/Renewal or Final Report Form
Example Informed Consent Forms
Below are examples of informed consent forms for various types of research conducted at Â鶹ÊÓƵ.
- General Informed Consent Form Template
- Syllabus Opt-In Statement Examples
- Interview Example
- Online Survey Example
- Experimental Design Example Placeholder
- Course Work Used for Research Example Placeholder
- Biomedical or Biospecimen Example Placeholder
- Parental Consent Form for studies involving minors template
- Adolescent Minors (7th grade and above) Assent Form template
- Young Minors (ages 7-10) Assent Form template template