The new guideline impacts sponsors, investigators and service providers involved in running clinical trials. Join this ICON webinar to gain the knowledge required to achieve compliance with the new regulatory regime, with a strong focus on data accuracy, security and operational efficiency of the trial.
Join Vesta Marciulioniene, Director, Global Regulatory Clinical Services, ICON Biotech; Cooper Brown, Senior Project Manager, DCT Solution Enablement, ICON; Berit Gorsøe Kjeldsen, Director, Project Management, ICON Biotech; and George Evgrafov, Senior Manager, Technology Quality Assurance, ICON, for the live webinar on Tuesday, November 28, 2023, at 10am EST (4pm CET/EU-Central).
For more information, or to register for this event, visit Clinical Trial Computerised Systems and Electronic Data – Lessons Learned Implementing the New EMA Guideline.
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