CRScube Inc. software

cubeBUILDER® provides an intuitive interface for sponsors, CROs, and academic institutions to access and rapidly build cubeCDMS®, cubeIWRS®, and cubePRO® system environments to conduct clinical trials electronically and securely on the cloud. cubeBUILDER® is free, easy-to-learn, and easy-to-use.

cubeCONSENT® provides a learning environment for subjects and ensures that the subject completely understands the trial prior to signing the Informed Consent Form (ICF). cubeCONSENT® is interoperable and integrated with the cubeCDMS® with subjects being automatically enrolled in cubeCDMS® upon signing the ICF.

cubeRBM® is a real-time monitoring solution that helps mitigate risk by planning and ensuring the quality of clinical trials by identifying, evaluating, monitoring and alleviating the risks that may affect the quality and safety of clinical trials. cubeRBM® collects the risks of each site participating in the clinical study in real-time through the EDC and evaluates and compares it with a unique index called SPI (Site Performance Index score). The data collected through cubeRBM® is visualized with charts and graphs, allowing users to identify clinically problematic sites through formal indicators.

cubePRO® is a mobile application used to collect ePRO (electronic Patient Reported Outcomes) data. Data is entered directly by participating patients which leads to a minimization in data reconciliation as the data is automatically synced with cubeCDMS®` database. cubePRO® is setup using cubeBUILDER® and can be equipped with edit checks which results in a reduction in errors and ensures that clean data is entered.

cubeCDMS® is a recognized compliant solution with the FDA`s 21 CFR Part 11. It ensures seamless accurate eCRF data collection with simple and efficient data management.