EU Clinical Trial Regulation

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Presented by

Merete Jørgensen,

About this talk

EU Clinical Trial Regulation: Balancing Requirements Related To Transparency And To Protection Of Personal Private Data And Commercially Confidential Data The session aims to cover an overview of the different requirements on transparency, the data protection regulation for personal private data, and the set-up for how commercially confidential data might be protected. The focus will be on the strategic view of achieving transparency and the utility of data in CTIS while ensuring EU remains attractive for clinical trials by ensuring sponsors commercially confidential information is protected.
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