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Office of Research Integrity

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Initial IRB Submission & Beyond

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Electronic IRB Submission System

E-IRB

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Survival Handbook

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Medical & Nonmedical IRB

IRB Meeting Dates

Medical & Nonmedical IRB

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Frequently Asked Questions (FAQs)

What Needs IRB Review?

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)

Nonmedical IRB Submission Prep Checklist [D152.0000] (PDF)

Sample Human Research Forms

Sample Applications and Protocol Development Resources

Interactive Tools

Dictionary of Institutional Review Board and Human Research terms

Acronyms and Abbreviations

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Office of Research Integrity

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405 Kinkead Hall
University of Kentucky
Lexington, KY 40506-0057
Phone: 859-257-9428
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