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  • About
  • Compliance
    • Multiracial Hands Making a CircleHuman Research Protections
    • Laboratory experimental mouse on the researcher’s handAnimal Care & Use
    • One dollar bills shaped to resemble the dollar signConflict of Interest
    • Airliner with a globe and autoloader (Export Controls concept image)Export Controls
    • Fingers holding a globe and lines showing network connectionsResearch Security & International Engagement
    • RCR & Research Misconduct
    • Human Stem Cell Research
    • Cannabis Research
    • Dual Use Research of Concern
    • Institutional Biosafety
  • Growth & Collaboration
    • Business People In A Boardroom MeetingCenters & Institutes
    • A group of people meeting against a backdrop of a mapTeam Scholarship Acceleration Lab
    • Planning Ideas Innovation Creativity Knowledge Vision ConceptResearch Development
  • Proposals & Awards
    • Light bulbs hanging downSponsored Projects Administration
    • Doctor pointing to a medical documentClinical Trials
    • Calculator, pen and spreadsheetContracts & Grants Accounting
  • Facilities & Services
    • 2 people looking at a computer screenElectronic Research Administration
    • Lab mice cagesUniversity Laboratory Animal Resources
    • MRI MachineUCI Shared Facilities List
    • Stack of wooden blocks with symbols reflecting health safety and environmentEnvironmental Health & Safety
  • Policy Library
» Human Research Protections » IRB Application Process
Human Research Protections
  • Contact Us
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  • Do You Need IRB Review?
    • Not Human Subject Research Self-Determination
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  • IRB Application Process
    • How to Submit IRB Applications
    • Lead Researcher/Principal Investigator Eligibility
    • Training & Education
    • Ethical Guidelines, Regulations and Statutes
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  • Single IRB (sIRB) Process
    • UCI is the Relying IRB
    • UCI is the Reviewing IRB
  • HRP Toolkit
  • Assessing Risks and Benefits
    • Levels of Review
    • Privacy & Confidentiality
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      • Protected Health Information (HIPAA)
      • General Data Protection Regulation (GDPR)
      • China’s Personal Information Protection Law
  • Subject Enrollment
    • Informed Consent
      • Required Elements of Informed Consent
      • Drafting the Informed Consent Form
      • Consent and Non-English or Disabled Subjects
      • Use Of Surrogate Consent In Research
    • Vulnerable Populations
  • Clinical Research
    • Data and Safety Monitoring for Clinical Research
    • Drugs and Biologics used in Clinical Research
      • Placebo-Controlled Studies
      • Expanded Access to Unapproved Drugs or Biologics
      • Right to Try: Unapproved Drugs or Biologics
      • Use of Controlled Substances
    • Devices Used in Clinical Research
      • Expanded Access to Unapproved Medical Devices
      • Humanitarian Use Devices
    • Human Gene Transfer Research
  • Ethnographic Research
  • Post-Review Responsibilities
  • ClinicalTrials.gov
  • IRB FAQs

IRB Application Process

ZOT IRB TIP! Refer to EQUIP's updated Do You Need IRB Review as a quick-start guide for what IRB review and documents apply to your research when submitting to ZOT IRB!

The PI WORKSHEET - New Study Submission - No Reliance was created to help investigators prepare for their protocol submission in ZOT IRB. Please review it for reference before submitting your IRB application.

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