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3 Important Takeaways from DIA 2017

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As explained in our previous blog titled 5 Tips to Make the Most of the DIA 2017 Annual Meeting, it’s important to plan appropriately when aiming to utilize and benefit from the information gleaned at conferences like DIA 2017.  Just like the theme of this year’s show – Driving Insights into Action…

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The Convergence of Reporting Standards and the Clinical Trial Industry

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The Clinical Data Interchange Standards Consortium (CDISC), FDA and the clinical trial industry are converging on ways to streamline and “…modernize the clinical research system.” With increasing adoption among clinical trials, research sponsors and investigators, clinical trial operations are taking note and heeding more clearly defined standards around collecting data…

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Consider the Cloud for Your Clinical Trial Systems

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While leveraging the cloud for advanced clinical trial systems once seemed like a “pie-in-the-sky” concept (pun definitely intended), with today’s technology, cloud computing is a practical and pragmatic way to approach housing, managing, analyzing, and sharing clinical trial data.  And even though technology has caught up to make cloud clinical…

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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.

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