Human Subjects - IRB
IRB Resources
- Submitting an IRB Protocol: Step-by-Step Instructions
- IRB Forms and Templates
- Does Your Research Require IRB Approval?
- Guidance for Researchers
- Human Subjects Data Security
- HSP Training
- Principal Investigator Responsibilities
- Faculty Advisor Responsibilities
- Good Clinical Practices
- UTA IRB Policies & Procedures
- Recruitment of UTA Students by External Researchers
- IRB Meeting Schedule and Roster
- Report a Concern
The University of Texas at Arlington, by action of the President, has established an Institutional Review Board (IRB) to review human subject research. This board is supported by Regulatory Services. The IRB reviews all research involving human subjects that is conducted or supported by the University of Texas at Arlington faculty, students or staff in order to determine that the rights and welfare of the human subjects are adequately protected. The IRB is guided by the ethical principles described in the 'Belmont Report' and by the regulations of the U.S. Department of Health and Human Services found at Title 45 Code of Federal Regulations, Part 46. The University of Texas at Arlington maintains an approved Federalwide Assurance (FWA) of Compliance with the Office for Human Research Protection (OHRP).
The University of Texas at Arlington's Federalwide Assurance (FWA) number is FWA00001762, expiring November 10,2027.
Please visit the electronic IRB submission system at https://mentis.uta.edu/public/#irb/index/index to submit all IRB applications, modifications, & continuing reviews.
You can report your concern or issue anonymously at:
https://www.uta.edu/php-lib/machform/view.php?id=4706.
Contact the Office of Regulatory Services for assistance or additional information: 817-272-3723 or regulatoryservices@uta.edu