clincase

clincase provides a fully featured, 21 CFR part 11 compliant EDC solution, giving both investigators and monitors a powerful yet easy-to-use environment for data entry and monitoring. clincase supports all the steps of the clinical trial process from translation of the clinical trial protocol to the consolidation of all collected trial data, ready for reporting and analysis. All these tasks are integrated within one seamless application.

A proven, off-the-shelf Solution

clincase has been specifically designed to fulfill the pharma industries desire to achieve more control over the EDC-based clinical trial process. As an off-the-shelf product clincase can be easily adopted by pharma companies, CROs and academic institutions of any size, utilizing existing employee skill sets and processes. This allows the sponsor to define their level of involvement in the conduct of the trial according to their existing capabilities. clincase helps drug development companies of any size to realize the cost benefits of EDC whilst minimizing the overhead associated with implementing a new technology.