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Considerations For Compliance With CTIS Submissions Under The EU-CTR
This article outlines the process for sponsors in transitioning from an EU-CTD to an EU-CTR CTIS submission process. It provides guidance on. ....
Alexandra Moylan
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Nelson Mullin Baltimore
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Michael Halaiko
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Clinical Trial Team
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While The European Medicines Agency
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European Economic Area
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Clinical Trial Information System
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Trial Regulation
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Trial Directive
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Data Protection Regulation
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European Medicines Agency
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Personal Data
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Confidential Information
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Plan For Addressing
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Clinical Trial
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