Research Involving Human Subject (IRB)


Getting Started Guidance Resources Training IRB Forms

Questions? Contact the IRB at

Research Involving Human Subjects

IRB Meetings IRB Committee Members
IRB Standard Operating Procedures (SOPs)
Updated 7/15/2016
IRB Non-Compliance SOP
IRB Researcher Manual
Updated 7/15/2016
HHS International Compilation of Human Subject Research Protections
45 CFR Part 46: Protection of Human Subjects HHS The Belmont Report

Guidance Resources

Frequently Asked Questions About the IRB IRB Research Summary Instructions
IRB Submission Procedure Research with Local School Districts
Video (IRB Review Process)
by Dr. Kenny
A Dozen Tips for a Successful IRB Application
Does My Research Require IRB Review
Helpful Flow Charts and Checklists


CITI Course in The Protection of Human Research Subjects
CITI IRB Quick Start Guide CITI IRB Training Instructions

IRB Forms

IRB New Application
Version 9/7/16
Addendum for International Research
Version 3/2/16
Addendum for Research Involving Children
Version 8/3/15
Addendum for Research Involving Pregnant Women/Fetuses/Neonates
Version 8/3/15
Addendum for Research Involving Prisoners
Version 7/21/15
Renewal Application
Version 7/15/16
Request for Change
Version 7/22/16
Unanticipated Event Form
Version 9/5/12
IRB Template Paper Informed Consent Form
Version 7/15/16
IRB Template Electronic Informed Consent
Version 7/15/16
Sample Video Consent
Version 6/20/2016
Letter of Access template/example
Version 6/21/13
IRB Assent Form