Skip to main
University-wide Navigation
Office of Research Integrity

Researchers

Getting Started    E-IRB    IRB Survival Handbook    Request A Consult

Frequently Asked Questions (FAQs)

What Needs IRB Review?
What Needs IRB Review? (Video)

Which Institutional Review Board (IRB) will review my research?

Human Subject Protection (HSP) Training FAQs

Guidance for Protocol Review

IRB Review Types

Informed Consent/Assent

FDA-Regulated Research

Clinical Trials

FDA Emergency Use (EU)

Single IRB Reliance for Research Collaborations

A Principal Investigator's Guide to Responsibilities, Qualifications, Records and Documentation of Human Subjects Research
(PDF)

HIPAA in Human Research

Data and Safety Monitoring

Other Human Research Review Committees

Quality Assurance/Improvement Program for Human Research Protections

Samples and Forms

Medical IRB Submission Prep Checklist [D152.0100]
(PDF)

Non-Medical IRB Submission Prep Checklist [D152.0000]
(PDF)

Sample Human Research Forms

Sample Applications and Protocol Development Resources

IRB Meeting Dates

IRB Membership Rosters

Disclaimer: Please note that due to recent unauthorized actions of others, the IRB rosters have been modified for posting effective 5/9/2024. If your sponsor or funding source requires a non-modified version, please contact Pam Stafford at pastaf3@uky.edu.

Interactive Tools

Dictionary of Institutional Review Board and Human Research terms

Acronyms and Abbreviations

Contact Us

Subscribe to the UK ORI/IRB Listserv

Contact ORI Staff

Email ORI

Request a Consult

Office of Research Integrity

Contact us

405 Kinkead Hall
University of Kentucky
Lexington, KY 40506-0057
Phone: 859-257-9428
University of Kentucky Homepage A link to return to the University of Kentucky Homepage
An Equal Opportunity University
Accreditation
Directory
Email
Privacy Policy
Accessibility
Disclosures
© University of Kentucky
Lexington, Kentucky 40506