Office of Sponsored Programs and Research Integrity

Research Involving Human Subject IRB


Getting Started

Guidance Resources


IRB Forms

Questions? Contact the IRB at

Research Involving Human Subjects

IRB Meetings

IRB Committee Members

PDF DocumentIRB Standard Operating Procedures (SOPs)
Updated 7/31/2017

PDF DocumentIRB Non-Compliance SOP

PDF DocumentIRB Researcher Manual
Updated 7/31/2017

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

PDF DocumentResearch with Local School Districts

PDF DocumentAdvertisement Guidance

PDF DocumentA Dozen Tips for a Successful IRB Application

PDF DocumentDoes My Research Require IRB Review
Helpful Flow Charts and Checklists

PDF DocumentDeception and Incomplete Disclosure

pdf documentScientific Review Handout

pdf documentTips for Classroom Research


CITI Course in The Protection of Human Research Subjects

PDF DocumentCITI IRB Quick Start Guide

PDF DocumentCITI IRB Training Instructions

IRB Forms

Word DocumentIRB New Application
Version 7/1/17

Word DocumentAddendum for International Research
Version 7/1/17

Word DocumentAddendum for Research Involving Children
Version 7/1/17

Word DocumentAddendum for Research Involving Pregnant Women/Fetuses/Neonates
Version 7/1/17

Word DocumentAddendum for Research Involving Prisoners
Version 7/1/17

Word DocumentRenewal Application
Version 7/1/17

Word DocumentRequest for Change
Version 7/1/17

Word DocumentUnanticipated Event Form
Version 9/5/12

Word DocumentIRB Template Paper Informed Consent Form
Version 7/18/17

Word DocumentIRB Template Electronic Informed Consent
Version 7/18/17

Word DocumentSample Video Consent
Version 7/1/2017

Word DocumentLetter of Access template/example
Version 6/21/13

Word DocumentIRB Assent Form
Version 7/1/2017