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IRB Policies & Procedures

This page is under construction and is incomplete.
This notice will be removed when the page is finalized.
Please contact the IRB office if you have any questions.

  • 1: Introduction
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  • 5: Informed Consent
  • 6: Initial IRB Review of Research
  • 7: Continuing Review of Human Subject Research
  • 8: Amendment of Human Subject Research
  • 9: Unanticipated Problems
  • 10: Research with Investigational Devices
  • 11: Vulnerable Populations
  • 12: Community-Based Research
  • 13: Transnational Research
  • 14: Deceptive or Incomplete Disclosure
  • 15: Research Using Surveys and Internet Research
  • 16: Health Record Research
  • 17: Genetic Materials
  • 18: Human Tissue and Data Repositories for Research Use
  • 19: Data and Safety Monitoring in Research
  • 20: Protocol Deviations and Noncompliance
  • 21: Suspensions and Terminations
  • 22: Institutional Reporting Requirements
  • 23: Cooperative and Collaborative Research
  • 24: Clinical Research