In order to support all study types and budgets, CROS NT boasts an EDC portfolio of both proprietary and industry leading technologies suitable for:
- Phase I studies where rapid study set-up time and low license fees makes it worthwhile considering EDC for small studies of short duration
- Phase II-III studies more comprehensive technologies that include integrated modules such as CTMS, randomization, drug supply management, RBM facilitation, reporting and medical coding
- Phase IV studies – simple EDC options with an intuitive interface and limited, adequate functionality and a cost that suits post-market budgets
- Medical Device studies – simple, low-cost but very robust with attractive interface for Investigators
We can provide IVR, eCOA and EDC integration solutions including data storage, HelpDesk and eLearning.
CROS NT can also offer a cloud-based eClinical application which is an integrated platform of EDC/eCOA/IWRS/CTMS. Combining an eClinical platform in the cloud with a centralized approach to clinical data, Sponsors can reduce set-up, training and HelpDesk costs and allow for easy data integration. A cloud-based solution allows for real-time study management access to data from mobile devices. This platform also allows Sponsors to facilitate Risk-Based Monitoring through Risk Management Metrics which is a series of reports to monitor data taking into account risk factors and categories in order to track study progression and solve critical situations.