Skip to content
Main Menu
About
Compliance
Human Research Protections
Animal Care & Use
Conflict of Interest
Export Controls
Research Security & International Engagement
RCR & Research Misconduct
Human Stem Cell Research
Cannabis Research
Dual Use Research of Concern
Institutional Biosafety
Growth & Collaboration
Centers & Institutes
Team Scholarship Acceleration Lab
Research Development
Proposals & Awards
Sponsored Projects Administration
Clinical Trials
Contracts & Grants Accounting
Facilities & Services
Electronic Research Administration
University Laboratory Animal Resources
UCI Shared Facilities List
Environmental Health & Safety
Policy Library
Search
Search
Generic filters
Search in title
Search in content
Main Menu
About
Compliance
Human Research Protections
Animal Care & Use
Conflict of Interest
Export Controls
Research Security & International Engagement
RCR & Research Misconduct
Human Stem Cell Research
Cannabis Research
Dual Use Research of Concern
Institutional Biosafety
Growth & Collaboration
Centers & Institutes
Team Scholarship Acceleration Lab
Research Development
Proposals & Awards
Sponsored Projects Administration
Clinical Trials
Contracts & Grants Accounting
Facilities & Services
Electronic Research Administration
University Laboratory Animal Resources
UCI Shared Facilities List
Environmental Health & Safety
Policy Library
»
Human Research Protections
»
IRB Members
Human Research Protections
Page Menu
Contact Us
HRP Staff Directory
Office Hours
I-GREAT
Do You Need IRB Review?
Quality Improvement Project vs. Research
Self Exempt & UROP
Case Reports
Single IRB (sIRB) Process
UCI as the Relying IRB
UCI as the Reviewing IRB
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
Artificial Intelligence and Human Subject Research
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
Data Security
Protected Health Information (HIPAA)
European Union General Data Protection Regulation (EU GDPR)
China’s Personal Information Protection Law
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
ClinicalTrials.gov
Post-Review Responsibilities
IRB FAQs
IRB Forms
IRB Members
Scroll To Top