Trial Master File

Trial Master File

Welcome to MAESTRO Help: Trial Master File.  This section provides information on the document tracking features in the MAESTRO Clinical Trial Management System (CTMS).  Features covered include:

• Understanding the document tracking module capabilities
• Configuration/setup (creating Master Documents)
• Defining study-specific rules for documents using flags
• Entering/updating documents
• Standard reports in this module

Every clinical trial has associated regulatory documents that need to be tracked by the teams managing the trial (a.k.a. study).  The Trial Master File Module of MAESTRO provides study sponsors (and other team members with access rights to the module) with an efficient, centralized management tool for tracking regulatory compliance of, and providing access to e-copies of, those study-related documents.