Office of Research IRB Standard Operating Procedures - Office of Research

IRB Standard Operating Procedures

Standard Operating Procedures for Researchers

  • HRP-013
    Legally Authorized Representatives, Children, and Guardians
  • HRP-055
    Financial Conflicts of Interests
  • HRP-090
    Informed Consent Process for Research
  • HRP-091
    Written Documentation of Consent
  • HRP-092
    Clinical Trials Recruitment Websites
  • HRP-093
    Requirements for Investigators Conducting Clinical Trials and Clinical Investigations

Standard Operating Procedures for IRB Administration

General

  • HRP-001
    Definitions
  • HRP-012
    Observation of the Consent Process
  • HRP-013
    Legally Authorized Representatives, Children, and Guardians

Management of Incoming Information

Non-Committee Review

  • HRP-030
    Designated Reviewers
  • HRP-031
    Non-Committee Review Preparation
  • HRP-032
    Non-Committee Review Conduct
  • HRP-033
    Designated Faculty Reviewers
  • HRP-034
    Designated Faculty Review Conduct

Committee Review

Review Process

  • HRP-050
    Conflicting Interests of IRB Members
  • HRP-051
    Consultation to the IRB
  • HRP-052
    Post-Review
  • HRP-054
    Institutional Conflicts of Interest
  • HRP-055
    Financial Conflicts of Interests
  • HRP-056
    PPM 230-05 Public Health Service Regulations on Objectivity in Research
  • HRP-057
    University of California Policy on Financial Conflicts of Interest
  • HRP-058
    IRB Reliance When UC Davis Relies on an External IRB
  • HRP-059
    IRB Reliance When UC Davis is the IRB of Record

Periodic Tasks

Records

Committee Management