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   IRB GUIDEBOOK & INFORMATION RESOURCES



Federal Government Resources:
 

1. IRB Guidebook

2. Food and Drug Administration - Guidance for Institutional Review Boards and Clinical     Investigators

Other Resources:
 

1. Public Responsibility in Medicine and Research (PRIM&R)

2. On Being A Scientist: Responsible Conduct In Research (from the National Academy of Sciences)

Download Forms

  • Initial Application  Initial Application form
  • Consent Forms  Consent form
  • Addendum Application  Addendum Application form
  • Renewal Application  Renewal Application form
  •   Closure Application form
  •   Authorization Agreement form
  •   Non-Human Subject Research form
  •   HIPAA Authorization form

Quick Links

  • When is IRB required?
  • Initial Application
  • Addendum Application
  • Renewal Application
  • Full Board Meeting Dates
  • IRB Departmental Liaisons


External Links

  •  

    HIPAA
  • NIH
  • Federal Wide Assurance
  • Food an Drugs Administration: IRB guide
  • Public Responsibility in Medicine & Research

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