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Stefanie de Lange has a strong background in regulatory affairs within the medical industry. Stefanie has served as a Senior Manager in both Regulatory and Medical Affairs roles at Lohmann & Rauscher GmbH & Co.KG. Additionally, Stefanie has previous experience as a Project Manager at IFOM, University Witten/Herdecke. In their current role, Stefanie oversees the approval of medical products in accordance with EU regulations and leads the transition from MDD to MDR for the company's entire product portfolio.