Join Adaptive Clinical at the 7th Annual Clinical Data Integration and Management Conference

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Adaptive Clinical Systems is pleased to attend this year’s Clinical Data Integration and Management Conference. Designed specifically for heads, directors and VPs of Data Management and Clinical Operations, this year’s Clinical Data Integration and Management conference will focus on data mining, dealing with data standards, the pros and cons of risk-based monitoring, and the…

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Adaptive Clinical will be at the 7th Annual Crown Congress in Philadelphia on January 23 – 25. We welcome you to join us!

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Adaptive Clinical Systems is pleased to attend the upcoming Crown Congress Conference in Philadelphia, PA.  The Conference will be held on January 23rd through the 25th, 2018, at the Westin Philadelphia and will include numerous workshops to help senior-level decision-makers learn how clinical trials are evolving and how to be…

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Going to SCOPE Summit 2018? Adaptive Clinical Systems will see you there!

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Adaptive Clinical Systems is pleased to be an exhibitor in Cambridge Healthtech Institute’s Ninth Annual SCOPE Summit 2018, being held February 13-215, 2018 in Orlando, Florida. The 9th Annual SCOPE Summit, taking place February 13-15, 2018 in Orlando, FL, will offer three stimulating days of in-depth discussions in 18 different conferences,…

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Interested in improving your clinical trial data integration?  Click here to learn about our Adaptive eClinical Bus Solution, or contact us to learn more.

Improving clinical trials interoperability with the Adaptive eClinical Bus Solution

Our Adaptive eClinical Bus Solution is a secure, validated, compliant (FDA CFR 21 Part 11 and GxP), and cost-effective solution for clinical data integration – specifically designed to improve the way EHR and EMR systems communicate with each other to save you time and money.

Our software helps:

  • Eliminate duplication of data by capturing and transmitting electronic source data
  • Auto-populate electronic study forms from EHRs
  • Reduce transcription errors and improve the quality of data
  • Encourage entering source data at the point of care
  • 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

Discover how to easily improve your clinical trials interoperability and increase the efficiency of your operation, from shortened setup times to streamlined process improvements. Click here to learn more or contact us today.