Data capture and management in electronic and hybrid studies
Data security
21 CFR Part 11 compliance
User-friendly interface
Quick-responding tech support

Electronic case report form of trial subject: the primary tool for data capture.

  • CRF designer: forms, rules, and automatic check adjustment
  • Roles and access levels for trial participants
  • Integration with MATRIX IWRS and other solutions
  • Scheduling and tracking patient visits and detecting protocol deviations
  • Built-in checks of laboratory data according to normal ranges
  • Online reports
  • Automatic data validation
  • External data import from central laboratories, patient diaries and other sources
  • Query management
  • Data coding according to MedDRA, WHO Drug, and project specific dictionaries
  • Presenting data in easy-to-read format
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