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QUICK LINKS
  • Research Home
  • Office of the Vice President for Research
  • Research Development
  • Sponsored Programs
  • Export Control
  • Research Integrity
  • Comparative Medicine
  • Research Accounting
  • Technology Development
  • Research Communications
  • Postdoc Affairs
  • Community
  • Clinical Research
  • Research Cores
  • Research Interest Groups
  • Research Administration
  • Economic Development
  • DOR Staff Directory
Research Administration
  • Research Development
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  • Technology Development
  • Export Control
 
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IRB Policies & Procedures

compass pointing toward integrity

10.3 Research Integrity / Institutional Review Board

  • 10.3.1 Human Research Protection Program- Governing Principles, Policy and Organizational Structure
  • 10.3.2 Research Subjects with Cognitive Impairment
  • 10.3.3 Defining Human Subjects Research
  • 10.3.4 International Research
  • 10.3.5 Serious Adverse Event and Unanticipated Problems Reporting
  • 10.3.6 Children in Research
  • 10.3.7 Disclosure and Use of PHI in Research
  • 10.3.8 University Students as Research Subjects
  • 10.3.9 Closing an IRB Approved Study
  • 10.3.10 Informed Consent
  • 10.3.11 Waiver of Informed Consent
  • 10.3.12 Use of Drugs and Biologics in Human Subjects Research
  • 10.3.13 Use of Devices in Human Subject Research
  • 10.3.14 Continuing Review of IRB Approved Studies
  • 10.3.15 Protocol Deviations
  • 10.3.16 Research Registries and Repositories
  • 10.3.18 Institutional Authorization Agreements (IAA) and Reliance Agreements
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