The FDA is interested in clinical data interoperability. Shouldn't you be? Join our November 12th Webinar to learn how to save time and money on your clinical trials through streamlined data integration.
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The FDA is interested in clinical data interoperability. Shouldn't you be?
There's Still Space Available!  Learn how to:
Improve Your Clinical Trial Operation through EHR/EMR Integration
A free webinar on Thursday, November 12, 2015  |  2:00 - 2:30 PM EDT
Dear Camille,

You are invited to attend a free webinar on how to "Improve Your Clinical Trial Operation through EHR/EMR Integration” The webinar takes place on Thursday, November 12th at 2:00 p.m. EDT.
Click Here to Register for this FREE 30-minute Webinar: Thursday, November 12th at 2pm EDT
This 30-minute webinar will show you how easily and effectively the Adaptive eClinical Bus can integrate your clinical trials data and provide you with all of the benefits of a validated, standards-based solution that improves your research.

In 2013, the FDA published a final guidance on ‘‘Electronic Source Data in Clinical Investigations’’ which encourages use of electronic source data in the conduct of clinical trials.  The electronic capture of data from EHRs and healthcare devices, such as electrocardiogram management systems, digital imaging and mobile health devices, as well as electronic Patient Reported Outcomes Instruments has the potential to improve the reliability, quality, traceability, provenance, and integrity of data from electronic source to regulatory submission.

The Adaptive eClinical Bus® provides a cost-effective and seamless integration of EHR/EMR, EDC, CTMS,medical device, and other data that supports the FDA's guidance and provides all of the benefits cited by the FDA including:
  • Eliminating duplication of data by capturing and transmitting electronic source data
  • Auto-populating  electronic study forms from EHRs
  • Reducing transcription errors and improving the quality of data
  • Encouraging entering source data at the point of care
  • Facilitating remote monitoring of data to reduce the number of onsite visits
  • Improving site monitoring to minimize the need for cross-reference data in multiple sources
  • Making it easier for investigators to conduct clinical research
  • Facilitating the inspection and reconstruction of clinical investigations by FDA

Discover how to easily improve the efficiency of your clinical trials, from shortened setup times to streamlined process improvements.


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