Getting Started
E-IRB
Survival Handbook
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IRB Meeting Dates
IRB Member Rosters
What Needs IRB Review?
Which Institutional Review Board (IRB) will review my research?
Human Subject Protection (HSP) Training FAQs
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
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
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Contact ORI Staff
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