A trial master file checklist can help ensure that the content required for regulatory compliance is included in your organization’s TMF and that all requisite activities are effectively monitored and recorded.
MasterControl offers a complimentary downloadable trial master file template above in Excel spreadsheet format. The TMP template is designed to streamline the management and collection of TMF documentation from study initiation to study closeout.
MasterControl developed the TMF template to aid companies that have not yet invested in a TMF management software solution and/or are looking to augment inefficient paper-based TMF processes. It includes a complete listing of all TMF artifacts found in the TMF Reference Model and an explanation of the purpose of each item. The TMF template is based on the TMF Reference Model Version 3.0, which was released by the Drug Information Association’s TMF Working Group in June 2015.
A TMF software solution can facilitate the real-time management of a trial master file checklist and improve visibility into the status of all TMF activities. If you’re looking to implement a reliable TMF software solution, there are critical functionalities that must be considered. At minimum, an effective and dependable TMF solution should offer:
- A TMF Reference Model-based trial master file checklist.
- A document management configuration of TMF document types, trial master file checklist templates, metadata, version control, lifecycle management, routes and user roles for all TMF artifacts.
- A secure collaboration environment for sharing and exchanging clinical trial master file content with both internal teams and external contributors (i.e., sponsors, CROs, study sites, etc.).
- System notifications that are triggered after trial master file checklist milestones have been met and/or when task assignments have been completed.
The cloud-based MasterControl Clinical Excellence™ software solution suite streamlines the management of clinical trial master file documents and tasks and maximizes the connectivity and reuse of clinical research data. MasterControl clinical solutions are specifically engineered to facilitate: - Streamlined collection and control of TMF documents, artifacts, processes, tasks and site data on a single platform throughout the clinical lifecycle.
- Integrated study management.
- Seamless harmonization with quality management processes.
- Product lifecycle excellence through every stage of your clinical research and product development lifecycle.
- Adherence to the TMF Reference Model industry standard configuration.
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