For more than a decade, Adaptive Clinical Systems has delivered a data interoperability solution for clinical trials. With the intelligent middleware of the Adaptive eClinical Bus®, customers can add new systems while still retaining legacy data sources to maintain flexibility in selecting the best partners for any given trial.

Adaptive Clinical Systems is an eClinical Technology Solutions Company providing data flow

Integration Optimization Interoperability Innovation

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Simplified Workflow


Adaptive Rules Engine


Adaptive Connectors


Take eSource to the Next Level


Seamless Web & Voice Interface


Reduce Data Management Overhead


Imaging Integration


Leverage Real-time Analytics


Direct Data Capture

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® provides connections to roughly three quarters of all Public Health Information found in electronic health records and electronic medical records managed by Epic Systems Corporation and Cerner Corporation, and we can quickly connect to any other source of digital information. 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 Systems has been named as a Top eClinical Trial Management Solution Provider by PharmaTech Outlook. See the story here.

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

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