Features
Complete EDC Platform
Everything you need to run clinical trials efficiently and compliantly.
eCRF Builder
Design electronic Case Report Forms with an intuitive drag-and-drop builder. Support for text, number, date, dropdown, radio, checkbox, file upload, calculated fields, and more.
Data Validation
Built-in validation rules ensure data quality at the point of entry. Range checks, required fields, format validation, and cross-field edit checks.
Query Management
Raise, track, and resolve data discrepancies. Full audit trail of all query activity with a complete workflow: Open, Answered, Closed, Reopened.
Audit Trail
21 CFR Part 11 compliant immutable audit trail. Every data change, login, export, and action is logged with timestamp, user identity, old/new values, and reason.
Role-Based Access
Granular permissions for PI, CRC, CRA, Data Manager, Statistician, Monitor, and Viewer roles. Site-level data segregation for multi-site studies.
Data Export
Export data in CSV or JSON format. CDISC ODM-compliant data structure for easy SDTM mapping and regulatory submission preparation.
Visit & Event Scheduling
Define study events and visits with day offsets. Automatically generate form instances for each subject-event-form combination.
Multi-Site Support
Manage multiple sites within each study. Site-level data segregation ensures that each site only sees its own subjects.
Reports & Analytics
Monitor enrollment, form completion rates, query resolution times, and data quality with comprehensive reports and visual dashboards.