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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 , Nelson Mullin Baltimore , Michael Halaiko , Clinical Trial Team , While The European Medicines Agency , European Economic Area , Clinical Trial Information System , Trial Regulation , Trial Directive , Data Protection Regulation , European Medicines Agency , Personal Data , Confidential Information , Plan For Addressing , Clinical Trial ,

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. ....

Michael Halaiko , Alexandra Moylan , European Economic Area , Clinical Trial Information System , Trial Regulation ,