• Investigator instructions
• Policies & Procedures
  • Statement of Authority and Purpose
  • General Administration (100)
  • IRB Organization (200)
  • Functions and Operations (300)
  • Review of Research (400)
  • Reviews Requiring Special Considerations (500)
  • Noncompliance (600)
  • Informed Consent/ Authorization (700)
  • Quality Assurance (900)
  • Other IRB Reviewed Protocols (1100)
  • Confidentiality/ Privacy (1200)
  • Emergency Use (1300)
• RSPP-sponsored workshops
• Send us your suggestions
• IRB Registration
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RSPP/IRB Policies and Procedures – Functions and Operations

• Research Submission Requirements (FO 301)
• Research Exempt from IRB Review (FO 302)
• Administrative Review & Distrubition of Meeting Materials (FO 303)
• IRB Meeting Administration (FO 304)
• Documentation & Document Management (FO 305)
• Review of Medical Records and/or Databases for Research Purposes (FO 306)