Researchers

Getting Started Website

What Needs IRB Review?Video

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

IRB Review Types

Informed Consent/Assent

FDA-Regulated Research

Clinical Trials

Single IRB Reliance for Research Collaborations

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

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

Human Research Forms

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

HIPAA in Human Research

Human Subject Protection (HSP) Training FAQs

Data and Safety Monitoring

Sample Applications and Protocol Development Resources

Other Human Research Review Committees

IRB Survival Handbook (IRB Guidance from A to Z)

Quality Assurance/Improvement Program for Human Research Protections

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.