MATRIX CTMS

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