How do I know if I am conducting research with human subjects?
Why is my research subject to review?
How do I decide which application to use?
What training am I required to do before submitting my application?
Where can I get assistance?
How do I submit my application for review by the IRB?
When do I submit my application?
How will my application be reviewed?
Who will review my application?
What if my research project will be conducted at another institution?
What if I am not a UNT faculty member, but I want to conduct my research at UNT?
What happens if I don’t comply with UNT policy or federal regulations?
IRB Guidelines
Administration of the UNT IRB
Minimal Review Application
Expedited or Full Board Review Application
IRB Informed Consent Forms and Notices
Template A: Faculty/Staff Investigator and Adult Subjects
Template B: Faculty/Staff Investigator and Minor Subjects
Template C: Student Investigator and Adult Subjects
Template D: Student Investigator and Minor Subjects
Template E: Informed Consent Notice — Faculty/Staff Investigator and Adult Subjects
Template F: Informed Consent Notice — Student Investigator and Adult Subjects
Template G: Faculty/Staff Investigator with HIPAA Authorization
Template H: Student Investigator with HIPAA Authorization
Modification Request Form
Renewal Request and Progress Report Form
Final Report Form
IRB Guidance re Data and Safety Monitoring Plans
IRB 101 - Human Subjects Research and the UNT IRB
For information regarding availability of IRB 101, contact Boyd Herndon, Director of Research Compliance, at boyd.herndon@unt.edu.
Patricia Kaminski, Ph.D., IRB Chair, Psychology
Kathleen Duffy, Community Member
Rebecca Glover, Ph.D., Educational Psychology
Paolo Grigolini, Ph.D., Physics
Lisa Henry, Ph.D., Anthropology
David Hill, Ph.D., Kinesiology, Health Promotion, and Recreation
Debbie Rohwer, Ph.D., Music Education
Richard Smith, Ph.D., Behavior Analysis
Chad Trulson, Ph.D., Criminal Justice
Mark Vosvick, Ph.D., Psychology
*Brian Gladue, Ph.D., UNT Health Science Center
(*member for review of IRB applications with biomedical issues)