Getting Started
E-IRB
Survival Handbook
Request a Consult
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
Principal Investigators (PI) Guide for Human Research (Responsibilities, Qualifications, Records, and Documentation)
HIPAA in Human Research
Data and Safety Monitoring
Other Human Research Review Committees
Quality Assurance/Improvement Program for Human Research Protections
IRB Application Submission Prep Checklists
Sample Human Research Forms
Protocol Development Resources
View the Dictionary
View Acronyms & Abbreviations
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Contact ORI Staff
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