Our mission is constant data quality improvement and clinical trials management process optimization to help you manage your trials in the most efficient way.
Total control of your trial from eCRF design to final data export
Various reports generation
Database setup and data verification with manual and automated tools
Detailed eCRF design in accordance with study protocol
Team of data management specialists with profound experience in clinical trials
Quick adjustments to protocol alterations
Use EDC and IWRS system to gain total control of your data. Increase data quality while reducing risks and costs on randomization, data capture and management with Electronic Data Capture and IWRS system. Data capture and management within e-system.
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The system is validated and 21 CFR Part 11 compliant
Constant project progress control in real time
Data security: secure data storage in qualified data centers, data backups, access control to the system
EDC&IWRS system significantly saves time, efforts and financial resources in comparison to IVRS and paper CRF usage
Individual system adjustment for each study
User-friendly system does not require advanced technical skills. Access to the system from any device at any time
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