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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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The eClinical Forum is pleased to offer a recording of our free public webinar – the same as was presented to the FDA CDER Health IT Board on 6-April-2021 – to provide information on our 2 free tools: The “eCF Requirements”...

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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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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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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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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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