A CDISC EVENTS EXCLUSIVE PRESENTATION
 

Europe Interchange Keynote Presentation from Dr. Peter Marks, FDA

Watch the 2021 Europe Interchange’s final keynote address featuring Dr. Peter Marks, Director, Center for Biologics Evaluation and Research (CBER), speaking on, Facilitating the Development of COVID-19 Vaccines.

Access to all recorded Europe Interchange presentations are available to attendees for one year after the event.

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Global Regulatory Requirements

CDISC Standards are now required for regulatory submissions to FDA (U.S.) and PMDA (Japan).

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Use Cases for Clear Data

Learn how organizations have applied CDISC Standards to bring clarity to data.

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