IRB Policies and Procedures

All University of North Texas affiliates engaged in human subjects research that is reviewed and/or performed at the University of North Texas must comply with all applicable federal and state laws/regulations and the University of North Texas policies and procedures governing the conduct of human subjects research. Up-to-date standard operating procedures and policies for the IRB program are posted below. Please reach out to untirb@unt.edu with any questions.

IRB SOP 10.01 Roles, Responsibilities, and Composition of the IRB
IRB SOP 11.01 Researcher Roles and Responsibilities
IRB SOP 12.01 Compliance with Regulations and Policies
IRB SOP 13.01 Non-Human Subjects Research Determinations
IRB SOP 14.01 Funded Research Studies
IRB SOP 15.01 Pre-IRB Spending Requests
IRB SOP 16.01 Training and Education
IRB SOP 17.01 International (Transnational) Research
IRB SOP 18.02 Collaborative Research Studies
IRB SOP 19.01 Research with Native American or Alaskan Native Tribes
IRB SOP 20.03 Submission and Review of Requests for Approval

IRB SOP 21.01 Waiver of Informed Consent or Documentation
IRB SOP 22.01 Compensation to Research Participants
IRB SOP 23.01 Reporting Incidents
IRB SOP 24.01 Biohazard and Biosafety Review
IRB SOP 25.01 Research with a Data or Tissue Bank
IRB SOP 26.01 Radiation Safety Review
IRB SOP 27.01 Use or Disclosure of Protected Health Information for Research
IRB SOP 28.01 Conducting Research Using Crowdsourcing Platforms
IRB SOP 29.01 FDA Regulated Research
IRB SOP 30.01 ClinicalTrials.gov Registration
IRB SOP 31.01 Research on Sensitive Information
IRB SOP 32.01 Certificates of Confidentiality