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  • For Institutions
    • IRBManager Basics
    • Overview of the Study Review Process
    • Becoming A Signatory Institution
    • Navigating The CIRB For NCI Division of Cancer Prevention (DCP) Consortia Sites And Cancer Prevention Clinical Trial Network (CP-CTNET) Organizations
    • Create and Update the Signatory Institution Worksheet
      • Completing The Annual Signatory Institution Worksheet
      • Establishing Your Signatory Institution
      • Short Form Q & A
    • Creating and Updating the Annual Principal Investigator Worksheet
      • Establishing a Principal Investigator
    • How to Open a Study
      • Opening a Study
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      • Changing the PI on a Study
    • Submit a Study Closure
    • Report A Potential Unanticipated Problem Or A Serious Or Continuing Noncompliance
    • Request an Assent Waiver
      • Completing The Assent Waiver Worksheet
    • Notify the CIRB about the participation of an incarcerated participant
      • Completing The Notification of Incarcerated Participant Worksheet
      • Institution Q & A
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      • Finding Information Q & A
      • Guidelines For Permitted Boilerplate Language Additions
      • Individual Roles Within The CIRB
      • Institutions' Roles With The CIRB
      • Managing Your CTEP Registration
      • Oversight Q & A
      • Updating Your CIRB Institution Roster using RUMS
      • Updating Your CIRB Person Roster using RUMS
      • Viewing Your CIRB Roster
  • For Networks
    • Overview of the Study Review Process
    • CIRB Document Posting
    • Submitting Studies
      • Completing The Translation Application
      • Completing The Unanticipated Problem And/Or Serious or Continuing Noncompliance Submission Application
      • Completing The Waiver Of Consent Application
      • Completing the Amendment Review Application
      • Completing the Continuing Review Application
      • Completing the Initial Review Application
      • Determining Waiver Of Consent Requirements
      • End User Licensing Agreement (Eula) Consent Form Language Q & A
      • Review of Translated Consent Forms, PROs, and Other Patient-Facing Documents
      • Submitting Recruitment/participant Materials For Review
    • CIRB Meeting Schedules
  • For Board Members
    • Become A Board Member
    • Overview of the Study Review Process
    • Resources
      • Helpful URLs
      • IRBManager Training for Board Members
    • CIRB Meeting Schedules
  • Contact Us

IRBManager Training for Board Members

  • Read more about IRBManager Training for Board Members

ID.me Integration Guidelines for Existing CTEP-IAM Users

  • Read more about ID.me Integration Guidelines for Existing CTEP-IAM Users

Change Memo to SOPs

  • Read more about Change Memo to SOPs

How to Setup Your Computer for a Board Meeting

  • Read more about How to Setup Your Computer for a Board Meeting

CIRB Final Video Submission Form

  • Read more about CIRB Final Video Submission Form

CIRB CR Application

  • Read more about CIRB CR Application

Unanticipated Problem and/or the Serious or Continuing Noncompliance (UP/SCN) Submission Application

  • Read more about Unanticipated Problem and/or the Serious or Continuing Noncompliance (UP/SCN) Submission Application

Assent Waiver Worksheet

  • Read more about Assent Waiver Worksheet

Translation Application

  • Read more about Translation Application

CIRB_SOPs_31MAY2023

  • Read more about CIRB_SOPs_31MAY2023

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The NCI Central Institutional Review Board

401 N. Washington Street, Ste. 700
Rockville, MD 20850

The Central Institutional Review Board for the National Cancer of Institute is fully accredited by the Association for the Accreditation of Human Research Protection Program, Inc.