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NCI CTRP Subject Accrual User's Guide v3.9.1

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Application Support

If you have problems with the program or have suggestions for any of the CTRP User Guides, contact the NCI Clinical Trials Reporting Office using the information and guidelines provided in the Application Support section below.

About this Guide

This guide provides instructions for using the NCI Clinical Trials Reporting Program Accrual site to report accrual data for clinical studies registered with the CTRP (Clinical Trials Reporting Program).

Audience

This guide is designed for authorized users who want to view or submit accrual data for specific trials and sites.

Topics Covered

If you are new to NCI Clinical Trials Reporting Program Trial Registration Site, read this brief overview, which explains what you will find in each section.

Application Support

 

When submitting support requests, please include:

  • Your contact information, including your telephone number
  • The name of the application/tool you are using
  • The URL if it is a Web-based application
  • A description of the problem and steps to recreate it
  • The text of any error messages you have received

Contacting the Clinical Trials Reporting Office

If you have questions or comments regarding this document, or other CTRP topics, contact the Clinical Trials Reporting Office (CTRO) at ncictro@mail.nih.gov.

 

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