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EU Hybrid Workshop Announced

Oct 15-17 2024

  • 20 August 2024
  • Author: Adam Perkins
  • Number of views: 137
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Event date: 15/10/2024 - 17/10/2024 Export event

EU Hybrid Workshop Announced

Come join us for discussions on “How new and evolving technology is changing the roles in clinical research” at the eClinical Forum Hybrid Workshop, kindly hosted by Boehringer Ingelheim in Ingelheim am Rhein, Germany on October 15-17, 2024. The workshop will provide the usual updates and discussion on the eCF project teams and recent regulatory issues, as well as a day to focus on how the roles of the different participants in the clinical research path (from patient through to regulatory submission) have and will continue to change as technology evolves.

This workshop will be available for in-person and remote participation. There will be networking/social events on both evenings.  eCF Member companies can register up to 2 seats at this workshop. For those wishing to register for the US workshop  you can do so here : Oct 22-24: eCF US Workshop

2024 Autumn Workshop Topics: 

  • Regulatory updates: eCF meeting with EMA IWG
  • eCF Project Team updates and break-out discussions, including Audit Trail Review Analytics, Digital Health Technologies Governance, and Essential Metadata
  • Validation/Continuous Learning in AI products
  • Changing roles in e-clinical for: Patients, Sites, Clin-ops, Safety, Supply/logistics, Data managers, Statisticians, IT Support, Training dept, Auditors/QA, Medical Writing, Archivists.
    • We are looking for people to present their perspective on their changing role -- Please contact us!!

Workshop will take place at:

Boehringer Ingelheim:  Binger Str. 173, 55218 Ingelheim am Rheim, Germany

eCF Member companies may register up to 2 seats at this workshop by Oct 1; additional seats can be registered for a waiting list.  For more information or to register: eCF EU Hybrid Workshop Ingelheim, Germany Oct 15-17 2024 (eclinicalforum.org)

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eCF Free Public Webinar: Regulatory Requirements for Electronic Data/Systems for Clinical Trials, and associated site system assessments

eCF Free Public Webinar: Regulatory Requirements for Electronic Data/Systems for Clinical Trials, and associated site system assessments

The eClinical Forum is pleased to offer a free public webinar – to provide information on our 3 free tools: The “eCF Requirements” (Requirements for electronic data for regulated clinical trials), eSRA (Site eSource-Readiness Assessment), and ISF (Investigator Site File System) Assessment. 18-Sept-24: Registration Required.

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