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