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Institutional Review Board for the Protection of Human Subjects 
(Internal Use Only)

• IRB General Information
• IRB Consent Form Template
• IRB Consent Form Template (MS Word version)
• IRB Retrospective Review Template
• IRB Retrospective Review Template (MS Word version)
• IRB Committee Dates & Deadlines
• IRB Manual
• IRB Submission Guidelines
• Federal Wide Assurance Letter (FWA)
• Good Clinical Practice Letter
• Research Consent Policy & Procedure for limited English proficient patients
  • Research Consents
• Food and Drug Administration

Other Helpful Links

• Office for Human Research Protections (OHRP)
• Issues to Consider in the Research Use of Stored Data or Tissues.
• Are You Conducting Research Using Human Subjects?
• Research Repositories, Databases, and The HIPAA Privacy Rule
• OER Human Subjects Web Site