End-to-end electronic data capture, validation, discrepancy handling, SDV, and export capabilities for regulatory-compliant clinical trials.
Explore our documentation or contact our support team for questions about our solutions.
Centralized repository for reusable forms, controlled terminology, and CDISC variables to ensure consistency.
A graphical drag-and-drop CRF builder with full version control and real-time preview.
Powerful rule builder for edit checks, field dynamics, calculations, and real-time notifications.
Intuitive interfaces for site users to enter CRF data with real-time validation and status tracking.
End-to-end lifecycle management for both automatic and manual data discrepancies.
Dedicated workflow for SDV monitoring, including remote verification with source document upload.
A secondary review layer for Data Managers with PIN validation and discrepancy-raising capabilities.
21 CFR Part 11 compliant electronic signatures for CRFs with automatic revocation on data change.
Securely freeze forms to prevent updates or apply a final lock before database export for analysis.
Flexible engine to define and export customized, analysis-ready datasets in various formats.
Conclusion
Ensure your data is compliant, validated, and ready for regulatory submission at any stage of the trial.