HIPAA & PHI: Institutional Review Board (IRB) Office

• About
  • • About Overview
    • Contact Us
    • IRB Information
    • IRB Fees
    • News
    • Events
    • For Panel Members
    • IRB Metrics
• Submitting to the IRB
  • • Submitting to the IRB Overview
    • eIRB+
    • Getting Started
    • Study Team Members
    • Initial Studies
    • Modifications
    • Continuing Review & Closure
    • Reportable New Information (RNI)
    • Types of Reviews
• Resources & Guidance
  • • Resources & Guidance Overview
    • Protocol Templates & Forms
    • Consent Templates & HIPAA Requirements
    • Study Support Resources
    • Recruitment Materials & Guidelines
    • Policies & Guidance
    • Checklists & Worksheets
    • SOPs
• Compliance & Education
  • • Compliance & Education Overview
    • Education
    • Human Research Protections Training
    • Post-Approval Monitoring
    • Directed Reviews (For-Cause Audits)
    • Corrective and Preventive Action (CAPA) Plans
    • FDA Site Inspections
    • eIRB+ Compliance Workspace
• Reliance
  • • Reliance Overview
    • Single IRB Planning
    • Northwestern Serving as the IRB of Record
    • Northwestern Relying on an External IRB
    • SMART IRB & IREx
    • Northwestern Affiliates & Chicagoland Partners
    • Research at Northwestern Qatar
• For Participants
  • • For Participants Overview
    • Find a Research Study
    • Participant Resources
    • Participant Rights
    • Participant FAQs

Page Not Found

Unfortunately, the page you requested is not available.

Please visit the home page or use the search box in the header to find the page you are seeking.