Margareth Jorvid has over 30 years of experience in Regulatory Affairs and has worked at the Swedish Medical Products Agency (MPA) as well as large and small pharmaceutical companies, such as Roussel Nordiska, Hoechst Marion Roussel (Stockholm and Paris, France) and Neopharma. Since 2006, consultant in regulatory affairs and QA for pharmaceuticals, advanced therapies and medical devices through her company Methra Uppsala AB, LSM group. She is a member and honorary member of TOPRA (Organisation for Professionals in Regulatory Affairs), board member and TOPRA president from 2005-2006. MSc Pharm, MSc MTRA and MBA.
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