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Is your electronic health record system suitable for originating records that will be used in regulated clinical trials?

  • 2 March 2016
  • Author: Webmaster1
  • Number of views: 2075
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Is your electronic health record system suitable for originating records that will be used in regulated clinical trials?

Nearly 200 attendees participated in a webinar delivered by the eClinical Forum for ACRP.

The objective of the webinar was to allow attendees to:

  • Recognize the need to assess their electronic healthcare system to determine its appropriateness for originating and/or housing data that could be used in a regulated clinical research trial
  • Access a free tool to assist in assessing electronic health record systems

The presentation covered:

  • The rationale for assessing EHR / EMR Systems
  • The need for a standard mechanism to assess GCP compliance while minimizing burden for busy sites
  • The background to eSRA: Investigator Site System eSource-Readiness Assessment
  • How to access and use eSRA for free

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About this topic:  The final piece of the GCP renovation puzzle, revision 3 of ICH GCP.  Understand the background to the renovation, key changes and the philosophy of the changes in this one hour webinar.

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