Complete oversight of your trial documentation
Our eTMF solution provides trial teams with a user-friendly platform for efficient management of trial master files. With real-time tracking and quality check processes, teams can ensure compliance across the lifecycle of their clinical trials.
Stay in control
Real-time notifications for overdue or missing files
Full audit trail for inspection readiness
Automated workflows for reviews and signatures
Enhanced efficiency
Batch uploads for faster document handling
Seamless collaboration between sponsors, CROs and sites
Instant access to essential trial documents
Simplify your workflow, amplify your impact
Simplify your sites’ day-to-day operations
Managing Site Master Files (SMF) has never been easier. cubeTMF enables site staff to access, update and collaborate on documents in real-time, without the hassle of outdated and complex systems. Seamlessly connect sites and trial teams in one centralized platform, enhancing transparency and operational efficiency.
Why choose our eTMF solution?
Quality first
Enable quality checks and electronic signature processes, all fully traceable
Fully compliant
Built to meet global regulatory requirements and compatible with the DIA TMF reference model
Audit-ready
Quickly share relevant documents with auditors using a dedicated document storage area
Adapted to your needs
Customize review and signature workflows to match your requirements
Increased transparency
Visual indicators provide a quick overview of document status across your study
Centralized monitoring
Check compliance with easy-to-track progress
Spend less time configuring your TMF
Set up new studies in no time by reusing existing binder structures.
The CRScube difference
Developed with study managers
We carefully craft our solutions to address your challenges, simply
Continuous innovation
We’re always pushing boundaries to serve you better
Simple setup
Our solutions are easy to use and set up
Featured case studies
