CTMS Master
CTMS Master is a specialized clinical trial management system that enhances trial efficiency by improving user accessibility and communication. It features an integrated Site Visit Report tool that automates workflows, eliminates duplicate entries, and maintains customizable templates for project documentation. With over 100 metrics and 80 standard reports, it streamlines budget tracking and compliance management, ensuring informed consent tracking and effective communication throughout the trial process.
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Top CTMS Master Features
- Integrated Site Visit Report tool
- Automated workflow for SVRs
- Customizable project templates
- Extensive metrics and statistics
- Seamless integration with TrialMaster
- EDC
- IVRS
- eTMF systems
- Site-specific budget tracking
- Automatic payment approval options
- Manual payment approval options
- Invoicing on behalf of investigators
- Signature status tracking for consent
- Comprehensive trial communication logs
- Automated resolution tracking
- Corrective and preventative action tracking
- Standardized site documents
- Milestones and events tracking
- Ad hoc reporting capabilities
- Notification system for SVR process
- Customizable budgets per study
- Enhanced user accessibility and communication
