Empower your trial management
Our system equips clinical trial managers with the tools they need to excel. cubeCTMS offers real-time monitoring, efficient team communication, and swift status updates to stakeholders.
Detect signals early
Notification of issues that may impact data quality
Milestones and status tracking
Study budget management
Follow a plan
Workflow-led activities
Monitoring visit report tracking
Alerts for plan deviations
Simplify your workflow, amplify your impact
Micro tracking, macro reporting
Monitoring visit compliance
Define monitoring reports and track submissions
Progress tracker
Manage schedules and tasks with our calendar view
Study documents
Keep tabs on document submissions
Reports library
Access 10+ standardized reports
Study dashboards
Easily identify areas of focus with our study overview dashboards
EDC and TMF Integration
Get cleaner data with cubeCDMS and simplify document storage with cubeTMF
Monitor adverse events in CTMS
Discover the power of integration between cubeCDMS and cubeCTMS, with adverse events and other critical data automatically synchronizing.
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
Frequently asked questions (FAQs)
CRScube responds quickly to user requirements and incorporates relevant changes through regular updates, ensuring that users benefit from the latest features and improvements.
Junseok P.
Manager Clinical Data Management
Featured case studies
Optimizing clinical trial setup through intelligent automation and cubeCDMS integration
Discover how SevenTwoOne, a CRO, uses AI, RPA, Microsoft Office, and cubeCDMS to transform EDC development, reducing manual effort across specification creation, test data generation, EDC builds, QC, and paper survey processing.
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