Deploy and use in trials of any phase or therapeutic area.
Experience high-powered usability delivered via simple and intuitive design.
Benefit from fully scalable features for optimum data capture and management.
Per Therapeutic Areas
|Blood and blood-forming|
|* IND + Late Phase|
InteroperablecubeSolutions have been designed to perform with high-levels of data interoperability to minimize redundancies and errors.
CompliantcubeSolutions are compliant with industry regulations, such as the FDA’s 21 CFR Part 11.
User-friendlycubeSolutions all share in common simple and intuitively designed user interfaces that are both easy to learn and use.
Electronic data capture (EDC) solution for clinical trial data with additional features for streamlined database management.
Interactive web response system (IWRS) for real-time subject randomization and centralized drug stock/delivery management.
Clinical trial management solution with full and advanced features for centralized monitoring visit report workflow management.
Pharmacovigilance solution for case database management, safety reporting, and risk assessments.
A web and smartphone application for capture and management of electronic patient reported outcomes (ePRO).
A high-functioning, easy-to-use centralized web solution for building cubeCDMS, cubeIWRS, and cubePRO study environments.
cubeCDMS(EDC)-integrated solution for producing risk-based monitoring metrics and scores.
Fully scalable and secure electronic trial master file (TMF) repository and management solution.
Electronic informed consent with electronic signatures and metrics for sponsors.
|Number of clients||262||14||49|