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DIA Direct: Clinical Trials Regulation (EU) 536/2014: A Missed Opportunity? Assessing the Impact on EU Competitiveness in Global R&D Clinical Trials

Analyze the Clinical Trials Regulation 536/2014 and its impact on the European Union’s global clinical research.

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Overview

Join DIA's Clinical Research Community for this upcoming webinar. Analyze the Clinical Trials Regulation 536/2014 and its impact on the European Union’s global clinical research. At this webinar we will use clinical trial data to explore trends in market share, policy impacts, and the role of regulatory frameworks.

Featured topics

    • Analysis of the Clinical Trials Regulation (EU) 536/2014 (CTR) and its real-world impact
    • Explore trends in market share, policy impacts, and the role of regulatory frameworks such as GDPR and IVDR
    • Contrast EU performance with the post-Brexit UK and sheds light on the prospects for Europe’s clinical research sector

Who should attend?

The webinar is designed for clinical research professionals, clinical investigators, regulatory affairs professionals, and anyone interested in learning about clinical research regulations in the EU.

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