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Institutional Review Board (by sub category)
Overview   File Name
  • Human Subjects Research Guidelines for Investigators
  • Administrative Contacts
  • IRB Meeting Dates and Submission Deadlines
     
Policies and Procedures   File Name
     
Protocol Guidelines and Requirements   File Name
  • Clearance Sheet (used with all IRB submissions)
     
Adverse Events   File Name
     
Informed Consent Templates   File Name
     
Appendices   File Name
  • Belmont Report: Ethical Principles and Guidelines for the Protection of Human Subjects of Research
  • OHRP - Office for Human Research Protections Web Site
  • 45 CFR 46 - Protection of Human Research Subjects
  • FDA Web Site
  • 21 CFR 50 FDA Regulations -- Protection of Human Subjects
  • 21 CFR 56 FDA Regulations -- Institutional Review Boards
     
Other Forms   File Name
     

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