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For better and faster drug development, clinical trial operations must be managed strategically. That means it must incorporate a plan for – and the delivery of – true data interoperability no easy feat. Staying agile with expanding and evolving global regulations, study models like virtual and adaptive trials , mHealth, privacy and security concerns, and race to market only increase the need to seek a holistic clinical informatics solution. Clinical trial industry experts at Adaptive-Clinical Systems created the only proven technology that lets you quickly go from integration to interoperability across all eClinical tools through cloud-based,intelligent automated middleware that leverages a re-usable connector library, clinical rules engine intelligently moving and transforming data, fully validated and compliant with CFR 21 Part 11.

Clinical trial industry experts at Adaptive Clinical Systems created the only proven technology that lets you quickly go from integration to interoperability across all eClinical tools through cloud-based, intelligent automated middleware that leverages a re-usable connector library, clinical rules engine intelligently moving and transforming data, fully validated and compliant with CFR 21 Part 11.

Across CROs and systems, your teams get the timely information and intelligence they need and want to manage clinical trials holistically.

  • Truly real-time intelligence for risk management, oversight, financial management, and meaningful reporting
  • Operationalize, don’t just visualize – automate clinical processes with our proprietary rules engine
  • Optimize your eClinical investment – you choose your partners and eClinical BUS® brings you ultimate control with empowering insights
  • Imagine the InteroperabilityTM

Our important research and eClinical investments demand a partner like Adaptive Clinical Systems.

We deliver accurate, efficient, and validated data interoperability with the flexibility to use the best software tools for your study.

  • Fully validated platform with detailed audit logs & reports 
  • Fully compliant with HIPAA, GxP, & 21 CFR Part 11 
  • Standards-based for interoperability 
  • Easily implement an eSource data capture workflow 
  • Reusable SaaS components for quick installation 
  • Adaptive rules engine offers built-in clinical intelligence

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