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
- 13.004, Use of Human Subjects in Research*
*All University policies must be followed and can be found in the University Policy Manual