Alice K. Larsen is a skilled regulatory affairs professional with over 25 years of experience in the medical device and pharmaceutical industries. Currently serving as a Senior Global Regulatory Affairs Specialist at MagVenture, Alice K. Larsen focuses on improving regulatory procedures and driving submissions, while ensuring practical regulatory processes across the company. Previous roles include positions at Phillips-Medisize, ORIGIO, and Novo Nordisk A/S, where Alice K. Larsen contributed to the creation and maintenance of product design dossiers and global STED files for various medical devices. Educated at the University of Pharmacy in Copenhagen, Denmark, Alice K. Larsen holds a Master’s Degree in Pharmacy.
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