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    About

    Learn how the Institutional Review Board (IRB) can help you.

    Learn About IRB
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      • Meet the Staff Leadership
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  • Guidance

    Guidance

    Access current guidelines, policies, and other information needed to complete your tasks and projects.

    Browse Guidance
    • Reportable Information
    • Revised Common Rule
    • COVID-19
    • Getting Started
      • Does My Project Need IRB Review?
      • IRB Review Types
      • Study Submission Guidance
      • eIRB Page-level Help
      • Consent Toolkit
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    • Research Types
      • Clinical Trial Studies
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    • Other Guidance
      • Treating a Patient with an FDA Unapproved Drug or Device
      • Federal Policy for the Protection of Human Subjects (Common Rule)
      • Office for Human Research Protections (OHRP)
      • Health Insurance Portability and Accountability Act of 1996 (HIPAA)
      • US Department of Veteran Affairs (VA)
      • PHI Identifiers (PDF)
      • Belmont Report
      • Council for International Organizations of Medical Sciences (CIOMS)
      • Declaration of Helsinki (World Medical Association)
      • ICH Guideline for Good Clinical Practice (GCP)
      • Nuremburg Code
      • Conducting Research at the Atlanta VA
    • Frequently Asked Questions
  • Forms and Templates

    Forms and Templates

    Find the documents you need to support your research efforts.

    Browse Forms and Templates
    • Protocol Templates
    • Consent Toolkit
      • Instructions and Guidance
      • Short Forms
    • Waivers
      • Waiver of Consent
      • Waiver of Documentation of Consent
      • Waiver or Alteration of HIPAA
      • Waiver of Assent
      • Waiver of Parental Permission
      • Frequently Asked Questions
    • Food and Drug Administration
    • Other
  • Resources

    Resources

    We've compiled helpful resources to support you.

    Browse Resources
    • Log In to eIRB
    • Research Tools
      • Clinical Trial
      • Cancer Studies
      • FWA Registration Info
    • Training
      • Courses
      • Webinars
      • eIRB Training
    • Frequently Asked Questions
  • Members

    Members

    Find what you need for your research project.

    View Members Resources
    • 2018 Common Rule
    • eIRB Guidance and Videos for Member Review
    • Take 5 Training
    • Reviewer Checklists and Other Guidance
  • Participants

    Participants

    Are you a participant of a research trial or study? Access helpful information here.

    View Participant Resources
    • Participant Bill of Rights
    • Guidebook for Clinical Trial Participants
    • Looking for a Study?
    • Participant Frequently Asked Questions
    • Glossary
    • Información en Español
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Emory University Research Administration Institutional Review Board

Office of Research Administration
Emory University
1599 Clifton Road NE - 4th Floor
Atlanta, GA 30322

 404-727-3889
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