UT Arlington wants to assist researchers in every way possible with understanding the requirements for IRB submissions.

Please use the links below to explore the various resources and guidance available to assist you with the preparation of your IRB application.

Conducting Human Subjects Research at UTA

• UTA IRB Policies & Procedures 
  • Recruitment of UTA Students by External Researchers
  • IRB Terms and Definitions
• Coming Soon: Federal Regulations & Policies
• Does Your Research Require IRB Approval? 
• Submitting an IRB Protocol: Step-by-Step Instructions 
  • Principal Investigator Responsibilities
  • Faculty Advisor Responsibilities
  • IRB Forms and Templates
  • Required Documents for Protocol Applications 
  • Types of Research - Protocol Guidance 
  • Human Subjects Data Security
  • HSP Training 
  • IRB Review Pathways
  • IRB's Criteria for Approval
  • Coming Soon: Guide to Mentis (IRB Electronic Submission System)
  • Coming Soon: Tools & Resources Available to Researchers
  • IRB Meeting Schedule and Roster
• Closing a Protocol
• IRB Resources
• Multi-site Research & IRB Reliance 
• NIH Data Sharing and Management Policy
• Report a Concern

Biomedical Research, Clinical Trials, & FDA-Regulated Studies

• Good Clinical Practices
• HIPAA and Research
• ClinicalTrials.gov Guidance 
• Coming Soon: FDA Regulated Research

We welcome your suggestions for additional guidance and resources that we can include on our website!

Send us an email with your ideas to RegulatoryServices@uta.edu.