Simplifying the Process and Reducing Expense
Engineered for small- to mid-size CRO’s and Biotechs, Adaptive Clinical’s open source technology components have been used in 300+ clinical trials and are supported by thousands of developers worldwide. The Adaptive eClinical Bus® open architecture offers a rich array of solutions that easily integrate with any technology component of your study and enable seamless clinical systems interoperability.
Validated, Compliant, Standards-Based Tools to Increase Speed & Efficiency
All data – yours and your sponsor’s – are housed in strictest compliance with all privacy and security provisions of HIPAA, GxP, and 21 CFR Part-11. Detailed audit logs and reports allow your DM and QA staff to maintain rigorous oversight of all data at any time.
Data are maintained in native CDISC format at all times, enabling you to analyze content while the study is in progress. No need for costly data conversion expenses post database-lock: you can analyze interim snapshots of data at any time.
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.
Maintain Regulatory Compliance & Close Oversight
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 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.
No Capital Investment & Minimal IT Involvement
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.
Rapid Study Startup
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.