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eCF Americas Autumn Workshop 2024 Announced

October 22-24 2024

Event date: 22/10/2024 - 24/10/2024 Export event

eCF Americas Autumn Workshop 2024 Announced

Come join us for discussions on “How new and evolving technology is changing the roles in clinical research” at the eClinical Forum workshop, hosted by eClinical Solutions in Mansfield, MA on October 22-24, 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.

The workshop will be available for in-person participation only. 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 attend a remote eCF workshop, the eCF European workshop will have similar topics and will be live-streamed.  See information on that workshop here: EU Hybrid Workshop Announced (eclinicalforum.org)

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:

eClinical Solutions:  603 West St, Mansfield MA 02048

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 Workshop Mansfield MA Oct 22-24 2024 (eclinicalforum.org)

 

 

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eCF Webinar November: FDA warning letters for audit trail analytics

FDA warning letters tell us what went wrong, but what could your audit trail analytics program have caught earlier? Join our upcoming webinar for a practical, in-depth look at an FDA warning letter and learn how to identify missed signals, uncover blind spots, and strengthen your audit trail review program.

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