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Liesbeth Hof is a skilled professional with extensive experience in regulatory affairs and project management within the pharmaceutical industry. Liesbeth has worked at various companies such as AM-Pharma, ProPharma Group, Xendo, and Novartis, where Liesbeth has successfully led key milestones in regulatory processes and product development. Liesbeth has a Master's Degree in Medical Biology from Vrije Universiteit Amsterdam and has also received training at the Ministry of Health.