Top of page
Skip to main content
Emory University home
Emory UniversityInstitutional Review Board
  • Research Administration
  • About

    About

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

    Learn About IRB
    • Services
      • Teams and Meeting Schedules
      • IRB Target Turnaround Times
      • Outreach and Help Clinics
    • Frequently Asked Questions
    • Contact Us
      • Meet the Staff Leadership
      • Meet the Faculty Leadership
      • Meet the Research Protocol Analysts
      • Meet the Reliance Team
      • Meet the Education and Quality Assurance Team
      • Meet the IRB Members
    • AI/ML/Big Data Updates and News
    • Email Blasts
  • 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
      • Participant Facing Materials
    • Research Types
      • Clinical Trial Studies
      • Collaborative Research/Single IRBs/Reliance Agreements
      • Food and Drug Administration
      • International Research
      • Sponsor Investigator Studies
      • Sociobehavioral Research/Minimal Risk Studies
    • 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
Main content
  1. Home
  2. Forms and Templates
  3. eIRB
  4. Smart Forms

Smart Forms


  • New Study Submission (DOCX)
  • External Site submission (DOCX) (for WIRB/CIRB specific information, see Collaborative Research and External IRBs)
  • External Site addition (DOCX)
  • Modifications (DOCX) (aka Amendments)
  • Continuing Reviews (DOCX)
  • Combined Modification and Continuing Reviews (DOCX)
  • Reportable New Information (DOCX) (aka REs)
Back to main contentBack to top
Emory University home
  • Animal Care & Safety
  • Clinical Research
  • Conflict of Interest and Commitment
  • Environmental Health and Safety
  • Export Control
  • Institutional Review Board
  • Research Administration IT
  • Research Administration Services
  • Research Business Operations
  • Research Compliance and Regulatory Affairs
  • Research Grants and Contracts
  • Research Integrity and Compliance
  • Sponsored Programs
  • Strategic Operations and Training
  • Technology Transfer
  • Senior Vice President for Research
  • Research Administration
  • Emory Home
  • Emergency
  • Give to Emory
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
Copyright © Emory University
EO/AA Statement | Copyright | Privacy Statement
Back to top