University of North Texas 
IRB Forms and Templates
- About Human Subjects (IRB)
- IRB Protocol Submission
- IRB Forms and Templates
- Training and Education
- Multi-Institutional or Collaborative Research
- IRB Deadlines, Review, and Roster
- Human Subjects Research Determinations
- IRB Policies and Procedures
- External Resources
- Reporting a Concern
- Student Research Guidance
- Participant Compensation
- Human Subjects Recruitment
- External Resources
Unaffiliated Investigator Agreement Template
Unaffiliated Investigator Agreement Template
For use when a member of the research team is not part of an institution that has its own IRB.
Exempt Study Informed Consent Template
Expedited/Full board Consent Templates
Please click here for more details on review categories
Informed Consent Form - Adults - The consent form used for most studies that require a signature.
Informed Consent and Assent Forms - Parents and Minors - Parental consent/permission and child assent forms that are used for studies enrolling minors.
Informed Consent Form- With HIPAA Authorization - A consent form used when medical information (HIPAA) will be collected.
Informed Consent Notice - Electronic Consent - Consent form used for electronic surveys.
Recruitment Templates
Recruitment Message - An example of an email used to recruit participants for a human subjects research study. All elements of the template must be included but you may format the email as you wish.
Recruitment Flyer - A recruitment flyer seeking participation in a human subjects study. All elements of the template must be included but you may format the flyer as you wish.
Request for Consent Alteration/Consent Waiver
Request for Consent Alteration/Consent Waiver - Required form if you are using the Informed Consent Notice- Electronic Consent
form
Final Report
IRB Final Report - Request to terminate an active study. This form should be attached to a Cayuse "Closure" request.
Cayuse submission help document
Cayuse submission help - Cayuse IRB Initial Submission Guide