LEVERAGING KNOWLEDGE - DRIVING PERFORMANCE - DESIGNING THE FUTURE

Clinical Forum Teams work extensively with industry, healthcare organisations, academia regulators to link stakeholders and to facilitate the development of the environment for electronic clinical research. We have conducted surveys, developed tools, built an extensive base of knowledge of information relevant to the successful implementation of eClinical solutions.

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