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Disclaimer:The information presented in these works draws upon the combined understanding and knowledge of the eClinical Forum and is provided as an aid to understanding the environment for electronic clinical research. The opinions of the author(s) and the eClinical Forum do not necessarily reflect the position of individual companies.The content is unconfirmed and users should assess the content and opinions in the light of their own knowledge, needs and experience as well as interpretation of relevant guidance and regulations.

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

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Site Survey Presentation - DIA Clinical Forum Lisbon 13 Oct10 Site Survey Presentation - DIA Clinical Forum Lisbon 13 Oct10
Revisiting the eClinical Paradigm Investigational Site Perspectives on Clinical Trial Information Systems   As the healthcare and pharmaceutical technology spheres move closer together at the clinical research interface, the eClinical...

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EHR4CR: An Innovative Platform and Business Model for Re-Use of EHR for Clinical Research (ACDM UK 10Mar14) EHR4CR: An Innovative Platform and Business Model for Re-Use of EHR for Clinical Research (ACDM UK 10Mar14)
Improved access to patient data is key to managing bottlenecks in clinical research. The presentation gives an overview of one of the largest public-private partnerships aimed at providing adaptable, reusable and scalable solutions for re-using...

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eSRA: A Project to Self-Evaluate the GCP Compliance of Systems Holding Source Data for Clinical Trials (ACDM UK 10Mar14) eSRA: A Project to Self-Evaluate the GCP Compliance of Systems Holding Source Data for Clinical Trials (ACDM UK 10Mar14)

Investigators are frequently asked to complete sponsor-specific assessments of their EHR systems to enable sponsors to evaluate clinical trial data that will be sourced from these systems.

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