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ClinicalTrials.gov Record Maintenance Where the Institution is the Sponsor/Responsible Party

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This document provides a process for ClinicalTrials.gov Records Maintenance. Access to a CTMS, IRB applications, and their reporting tools are critical to ClinicalTrials.gov records maintenance. The Planning Report in the ClinicalTrials.gov Protocol Registration and Results System (PRS) Administrative console is critical for proactive maintenance of records.

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Disclaimer: This website was developed by members on the Clinical Trials Registration and Results Reporting National Taskforce to provide helpful information about registration and reporting of clinical trials. Taskforce members do not accept any responsibility or liability for the accuracy, content, legality, or reliability of the information contained on this website.