Researchers

E-IRB


Getting Started Website


What Needs IRB Review?


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


IRB Meeting Dates

  • Medical [PDF]
  • Nonmedical [PDF]

IRB Membership Rosters

  • Medical IRB Committee Members [PDF]
  • Nonmedical IRB Committee Members [PDF]
  • Combined Medical and Nonmedical IRB Committee Members [PDF]

Human Research Forms


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

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


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