Tracking log

The Tracking Log feature allows clinical trial teams to create and manage customized tracking logs for key regulatory documents, such as Financial Disclosure Forms (FDF), Form 1572, debarment statements, and more. It supports consistent record of documentation across study sites by using standardized tracking log templates created in LIBRARY.

With the Tracking Log functionality, teams can create and update documentation logs, maintain version history, analyze the details of who last modified each entry and when, and more. This helps monitor document status, identify missing or outdated records, and ensure regulatory compliance. It also contributes to readiness for audits and submissions to authorities like the FDA.

This section outlines the various actions available for tracking log setting and managing tracking log entries throughout the clinical trial lifecycle.