Adaptive Clinical Systems offers an industry-leading solution for your most complex clinical trial data interoperability challenges, the Adaptive eClinical Bus® and Adaptive DataVIEW. Decentralized and virtual trials add new data sources and new data types – and new operational complexity. Adaptive Clinical’s platform facilitates data workflows across all study partners and eClinical data sources.
The Adaptive eClinical Bus provides bi-directional data visibility from any eClinical tool in real time, including EDC, eCOA, CTMS, EHR, Medical Imaging, IRT, wearables, RWD and analytics/data visualization systems. Our flexible solution enables proprietary and third-party eClinical Systems to interoperate seamlessly. This saves CROs and Sponsors both time and money in terms of data entry, data verification, data harmonization and aggregated data visualization. With the Adaptive eClinical Bus®, you have actionable data faster. The Adaptive eClinical Bus is fully compliant with FDA CFR 21 Part 11, HHS 45 CFR Part 164, GxP and other regulatory guidelines.
Adaptive Clinical’s interoperability platform includes Adaptive DataVIEW™, a comprehensive, data visualization solution that complements and extends any data source from the Adaptive eClinical Bus to operationalize, gain insights from, exchange and visualize data more quickly. With Adaptive DataVIEW, any data source can be ingested in real-time. Reports and dashboards can be generated at the patient, site, study and program level. Sponsors and CROs can incorporate legacy data into operational dashboards without the need for convoluted data import and harmonization.
Adaptive Clinical has been in operation since 2012, and was founded by the original development team for a major eClinical informatics provider. Over the course of its operation, Adaptive Clinical has established relationships with eClinical vendors and EMR/EHRs covering 90% of all data generated in clinical trials. To date, the company has been able to integrate every digital data source requested by our clients.
Our software helps:
Eliminate duplication of data by capturing and transmitting electronic source data
Encourage entering source data at the point of care and reduce transcription errors
Facilitate remote monitoring of data to reduce the number of onsite visits
Improve site monitoring to minimize the need for cross-reference data in multiple sources
Make it easier for investigators to conduct clinical research
Facilitate the inspection and reconstruction of clinical investigations by FDA