UCLA Office of the Human Research Protection Program Menu
  • The UCLA IRB Office
    • Contact the UCLA IRB Office
    • About the UCLA IRB Office
      • UCLA Human Research Protection Program
      • IRB statistics (ORA Portal)
      • Close
    • About UCLA IRBs
    • IRB Descriptions
    • Meeting Calendars
    • Member Checklists
    • Member Rosters
    • IRB Member and Staff References
    • Review Fees
    • FWA & IRB Registrations
    • Human Research Policy Board
    • Human Research News
    • Close
  • For Researchers
    • Getting Started
    • Assessing Risks
    • Clinical Research Toolkit
    • HIPAA
    • Informed Consent Templates
    • IRB Reliance
    • Letter for Sponsor (PDF)
    • Bill of Rights
    • Policies and Guidance
    • Post Approval Reporting
    • Revised Common Rule
    • Electronic Submission Systems
    • Close
  • Quality Improvement and Education
    • Quality Improvement
    • Education and Training
    • CITI
    • Other Resources
    • Close
  • For Research Participants
    • Information For Research Participants
    • Información para Participantes en Investigaciones
    • Survey
    • Close
    • Close

About the OHRPP

  • Overview and Purpose
    • Three Units within the OHRPP
    • The Mission of the OHRPP
  • UCLA Human Research Protection Program
    • Overview of UCLA
    • Mission and Purpose of the Human Research Protection Program
    • Organization
    • Types of Research Reviewed
    • Concerns or Suggestions
    • Improving Human Research Protections at UCLA
    • Sufficient Resources

Search OHRPP Website

  • UCLA
  • OVCR
  • ORA
  • OCGA
  • EFM
  • OHRPP
  • ORDM
  • ORIS
© 2010 UCLA Office of Research Administration. All rights reserved  •   Contact Webmaster