Skip to content
Office of Research Wordmark
Skip Navigation
  • About
  • Compliance
    • Multiracial Hands Making a CircleHuman Research Protections
    • Laboratory experimental mouse on the researcher’s handAnimal Care & Use
    • AdobeStock 47352970 PreviewConflict of Interest
    • export-controls-conceptExport Controls
    • Undue Influence SquareUndue Foreign Influence
    • Responsible Conduct of Research
    • Human Stem Cell Research
    • Cannabis Research
    • Dual Use Research of Concern
    • Institutional Biosafety
  • Growth & Collaboration
    • Business People In A Boardroom MeetingCenters & Institutes
    • Stylized image depicting a group of people meetingTeam Scholarship Acceleration Lab
    • Planning Ideas Innovation Creativity Knowledge Vision ConceptResearch Development
  • Proposals & Awards
    • BulbsSponsored Projects Administration
    • Clinical TrialsClinical Trials
    • AccountingContracts & Grants Accounting
  • Facilities & Services
    • ERA Menu Image. 2 people looking at a computer screenElectronic Research Administration
    • Experimental Laboratory Mice Are Raised In The IVC, Individually Ventilated Cages System Protecting From Bacterial InfectionUniversity Laboratory Animal Resources
    • Tmf MiceTransgenic Mouse Facility
    • MRI MachineUCI Shared Facilities List
Office of Research Wordmark
Generic filters
Search in title
Search in content
Skip Navigation
  • About
  • Compliance
    • Multiracial Hands Making a CircleHuman Research Protections
    • Laboratory experimental mouse on the researcher’s handAnimal Care & Use
    • AdobeStock 47352970 PreviewConflict of Interest
    • export-controls-conceptExport Controls
    • Undue Influence SquareUndue Foreign Influence
    • Responsible Conduct of Research
    • Human Stem Cell Research
    • Cannabis Research
    • Dual Use Research of Concern
    • Institutional Biosafety
  • Growth & Collaboration
    • Business People In A Boardroom MeetingCenters & Institutes
    • Stylized image depicting a group of people meetingTeam Scholarship Acceleration Lab
    • Planning Ideas Innovation Creativity Knowledge Vision ConceptResearch Development
  • Proposals & Awards
    • BulbsSponsored Projects Administration
    • Clinical TrialsClinical Trials
    • AccountingContracts & Grants Accounting
  • Facilities & Services
    • ERA Menu Image. 2 people looking at a computer screenElectronic Research Administration
    • Experimental Laboratory Mice Are Raised In The IVC, Individually Ventilated Cages System Protecting From Bacterial InfectionUniversity Laboratory Animal Resources
    • Tmf MiceTransgenic Mouse Facility
    • MRI MachineUCI Shared Facilities List
» Human Research Protections » IRB Application Process
Human Research Protections
Human Research Protections Section Menu
  • Contact Us
    • HRP Staff Directory
    • Office Hours
  • Do You Need IRB Review?
    • Quality Improvement Project vs. Research
    • Case Reports
    • Self Exempt & UROP
  • Single IRB (sIRB) Process
    • UC IRB Reliance
    • How & What to Submit
    • Existing IRB Reliance Agreements
    • National Cancer Institute Central IRB (CIRB) Independent Review Process
    • NIH single IRB (sIRB) Review Policy for Multi-Site Research
  • IRB Application Process
    • Submitting the Application
    • Lead Researcher Eligibility
    • Training & Education
    • Ethical Guidelines, Regulations and Statutes
    • Other Institutional Requirements
    • Department of Defense Research Requirements
  • Assessing Risks and Benefits
    • Levels of Review
    • Privacy & Confidentiality
      • Data Security
      • Protected Health Information (HIPAA)
      • China’s Personal Information Protection Law
      • European Union General Data Protection Regulation (EU GDPR)
  • 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
    • ClinicalTrials.gov
    • Data and Safety Monitoring for Clinical Research
    • Drugs and Biologics used in Clinical Research
      • Placebo-Controlled Studies
      • Use of Controlled Substances
      • Expanded Access to Unapproved Drugs or Biologics
      • Right to Try: Unapproved Drugs or Biologics
    • Devices Used in Clinical Research
      • Humanitarian Use Devices
      • Expanded Access to Unapproved Medical Devices
    • Human Gene Transfer Research
  • Post-Review Responsibilities
  • IRB FAQs
  • IRB Forms

IRB Application Process

The below Protocol Preparation Checklist, was created to help investigators prepare for their protocol submission.  Please review this and other content under this section of the website before submitting your IRB application.

Download this PDF

protocol-preparation-checklist

© 2022 UC Regents
Scroll To Top