Site Map

• Home
• Who Needs to Apply
• The Application Process
  • Understanding the Purpose of the Review Process
  • Required Online Training
  • Preparing and Submitting a Proposal
  • Review Procedures
  • Next Steps and Responsibilities
• Writing a Proposal
  • The IRB Research Proposal Form
    • Additional Methods Considerations
      • Justification of Sample Size
      • Women and Minority Populations
      • Vulnerable Populations
      • Payments to Subjects
      • Recruitment & Advertisements
      • Deception in Research
      • Gathering Information About Individuals or Research on “Secondary Subjects”
      • Use of Biological Agents & Radioactive Isotopes
  • Documentation of Informed Consent
    • Informed Consent
      • Introduction
      • Function of the Consent Document
      • Required Elements
      • Additional Considerations
      • Consent Document Toolbox
        • Information About the Research
        • Additional Information
        • Risks
        • Benefits
        • Costs
        • Alternatives
        • Payment
        • HIPAA language at a 7th Grade Reading Level (where applicable)
        • Compensation for Injury
        • Voluntary Participation
      • Study-specific Concerns
        • Consent and Assent from Minors
        • Special Populations
        • Video and Audio Recording
        • Consent in Foreign Countries
        • Barriers to Consent
        • Waivers of Written Consent
        • Certificate of Confidentiality
• Compliance and Complaints
  • Complainant Protection Policy
  • Investigator Non-Compliance
  • Investigator Conflict of Interest
• Forms and Templates
  • IRB Research Proposal Form
  • Consent Forms
    • Participant Consent Template (with sample language)
    • Parental/Guardian Consent Template (with sample language)
    • Sample Child Assent Form (ages 7-13)
    • Sample Debriefing Form
    • Audio/Video Recording Signature Section
    • Sample Research Follow-Up Section
  • Research Project Change in Protocol Form
  • Research Project Continuation/Completion Form
  • Deviations from Approved Protocol
    • Adverse/Unanticipated Events Report
    • Protocol Deviation Report
  • Research Participant Complaint Form
• Useful Information and Links
• IRB Members and Schedule
• Contact the IRB
• Site Map