Leverage your proven, internally-developed and proprietary systems and retain your competitive edge. Adaptive Clinical’s eClinical Bus can easily integrate your technology into an interoperable, efficient, and accurate clinical trials system that streamlines your processes and improves data reliability.

A single source of data ensures access to the most up-to-date real-time information. Information is securely shared between systems and solutions. Automatic data checks, validation rules, and optional data-coding features save time and significantly reduce data entry errors resulting from paper CRF’s.

Our platform is available “hosted” for rapid deployment to as many sites as needed without any IT involvement and with the lowest TOC. You pay for access only while your study is in progress, thus enabling you to maintain little to no IT overhead between studies. An optional turnkey packaged software license is also available, if mandated by the sponsor.

Rest easy:  All data – yours and your sponsor’s – are housed in the strictest compliance with all privacy and security provisions of HIPAA, GxP, and FDA 21 CFR Part 11.  Furthermore, detailed audit logs and reports empower your DM and QA staff to maintain rigorous oversight of all data at any time.

Most studies can be set up and operational in less than two weeks using the system’s robust study setup tool. Or, if you prefer, you can import your existing eCRF templates using MS Excel or let us build your most complex field validation rules using our rules-editor.

As decentralized clinical trials become more complex, Adaptive DataVIEW™ provides holistic access to all your data from internal as well as external (CRO) sources via interactive reporting and visualization. Skip the drill downs, Adaptive DataVIEW has a unique “Single Click-Back” feature direct to the data source.