Office of Sponsored Programs and Research Integrity

Research Involving Human Subject IRB

 

Getting Started

Guidance Resources

Training

IRB Forms

Questions? Contact the IRB at IRB@uccs.edu

Research Involving Human Subjects

IRB Meetings

IRB Committee Members

PDF DocumentIRB Standard Operating Procedures (SOPs)
Updated 12/16/2016

PDF DocumentIRB Non-Compliance SOP

PDF DocumentIRB Researcher Manual
Updated 12/16/2016

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

Under
Construction

PDF Document    A Dozen Tips for a Successful IRB Application 
10/3/2016

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

PDF DocumentDeception and Incomplete Disclosure
Guidance

pdf documentScientific Review Handout

pdf documentTips for Classroom Research

Training

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 9/7/16

Word DocumentAddendum for International Research
Version 3/2/16

Word DocumentAddendum for Research Involving Children
Version 8/3/15

Word DocumentAddendum for Research Involving Pregnant Women/Fetuses/Neonates
Version 8/3/15

Word DocumentAddendum for Research Involving Prisoners
Version 7/21/15

Word DocumentRenewal Application
Version 7/15/16

Word DocumentRequest for Change
Version 7/22/16

Word DocumentUnanticipated Event Form
Version 9/5/12

Word DocumentIRB Template Paper Informed Consent Form
Version 7/15/16

Word DocumentIRB Template Electronic Informed Consent
Version 7/15/16

Word DocumentSample Video Consent
Version 6/20/2016

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

Word DocumentIRB Assent Form

 
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