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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
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Establishing Your Signatory Institution
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Creating and Updating the Annual Principal Investigator Worksheet
Establishing a Principal Investigator
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Opening a Study
Change the PI on a Study
Changing the PI on a Study
Submit a Study Closure
Report A Potential Unanticipated Problem Or A Serious Or Continuing Noncompliance
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Notify the CIRB about the participation of an incarcerated participant
Completing The Notification of Incarcerated Participant Worksheet
Institution Q & A
Boilerplate Language Q & A
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Individual Roles Within The CIRB
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Updating Your CIRB Institution Roster using RUMS
Updating Your CIRB Person Roster using RUMS
Viewing Your CIRB Roster
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Overview of the Study Review Process
CIRB Document Posting
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Completing The Translation Application
Completing The Unanticipated Problem And/Or Serious or Continuing Noncompliance Submission Application
Completing The Waiver Of Consent 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
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Overview of the Study Review Process
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Sarah Cannon
Nashville
Tennessee
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