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Sophie Poirette is a Regulatory Affairs Manager with extensive experience in medical device regulation and clinical affairs. Since August 2014, Sophie has been with Lohmann & Rauscher, initially serving as a Regulatory Affairs Coordinator, focusing on CE marking technical dossiers and risk management in accordance with ISO 14971. Prior roles include Clinical Affairs Engineer at CEREPLAS, where Sophie authored clinical documents and technical dossiers, and various internships in research and quality control. Sophie's education includes a Master's degree in Biology and Biotechnologies from the University of Lille 1, supplemented by leadership training.