Medical Products Agency Läkemedelsverket
Elisabeth Widmark currently serves as Gruppchef Parallellimport at Läkemedelsverket since April 2025. Prior experience includes roles as Senior Regulatory Affairs Consultant at RegFile AB and Senior Regulatory Manager at LINK Medical Research. Elisabeth held the position of Head of Regulatory Affairs and Medical Writing and served as both a Regulatory Affairs and GDP Consultant at Pharm Assist Sweden AB from January 2018 to March 2023. At Fresenius Kabi, Elisabeth functioned as National Safety Officer and Regulatory Affairs Manager from April 2005 to January 2018, where responsibilities included pharmacovigilance training and overseeing regulatory activities for medicinal products on a global scale. Elisabeth holds a Master of Science degree from Uppsala University, completed in January 2005.
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Medical Products Agency Läkemedelsverket
The Swedish Medical Products Agency is the Swedish national authority responsible for regulation and surveillance of the development, manufacturing and sale of pharmaceuticals, cosmetics and medical devices. The main task is to ensure that both the individual patient and healthcare professionals have access to safe and effective products and that these are used in a rational and cost-effective manner. The Swedish Medical Products Agency is one of the leading regulatory authorities in the EU. Together with these other EU authorities, we work to progress and develop the control of medicines within Europe. The Medical Products Agency is a government body under the aegis of the Ministry of Health and Social Affairs. Its operations are largely financed through fees.