Visit Staff-Only Access for IRB Procedures Manual ; Email Templates; Other

Checklists

• Consent Observation Checklist
• Continuing Review
• Exemption Eligibility
• Expedited Modification (job aid to verify review procedure)
  
  
• Informed Consent (medical: clinical studies)
• Informed Consent (medical: expedited/minimal risk)
• Informed Consent (nonmedical: surveys, social, behavioral, education research)
• Informed Consent (CIRB)
  
  
• Neonates
• Other Federal Agency Requirements:
  • Dept. of Defense (DoD), Dept. of Navy (DON)
  • Dept. of Education (ED)
  • Dept. of Energy (DOE)
  • Dept. of Justice (DOJ)
  • Environmental Protection Agency (EPA)
    
    
• Protocol - Medical
• Protocol - Expedited (initial review)
• Protocol - Chart Review (initial review)
• Protocol - Nonmedical
• VA Research; see Reviewing VA Research for additional requirements

Forms Concerning IRB Membership and Meetings

• Consultant Conflict of Interest Declaration
• IRB Member Conflict of Interest Declaration
  
  
• Confidentiality Agreement
  
  
• Determining if IRB Public Members are Unaffiliated
• Determining if IRB Members are Non-Scientists
  
  
• IRB Chair and Member Evaluation forms 

Other

• Exemption from IRB Review: Emergency Use of a Test Article
  
  
• HSR: Human Subject Research (HSR) Determination
• HSR: Determining when Organization is Engaged
  
  
• Meeting Preparation - Protocol Notes
• Procedure for Observation of Consenting Process
   
• Review of Scientific and Scholarly Validity, and Oversight - Academic Sponsor
• Review of Scientific and Scholarly Validity
• Scientific Review Protocol (for projects not otherwise undergoing scientific review)
  
  
• SIR Requirements for New, Continuing Review, Final Report
• VA: Reviewing VA Research