The cubeCDMS, a recognized solution for compliance with the FDA's 21 CFR Part 11, is the optimal solution to ensure seamless eCRF data collection and simple and efficient data management at the same time. Quickly detect and respond to factors that could reduce the likelihood of success in clinical trials with cubeCDMS, and lead clinical trials that start with data collection to success.
|Fully integrated with all of CRScube's solutions, Creates high quality data more easily and flexibly.|
|Reduce the time required for clinical trials.|
|It provides high efficiency through high risk mitigation.|
|Perfect security and data backup prevent the risk of data corruption and loss.|
|Short training time allows you to start clinical trials more quickly.|
Real-time data retrieve & download
Efficient and easy data management
Fast and accurate medical coding
Various Imports & Exports
Randomization and IP allocation.
Data interlocking based on shared database.
Risk-based monitoring based on eCRF data.
Case synced from eCRf data.
One-platform solution to build up cubeCDMS / cubeIWRS / cubePRO.