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Margareta Svanholm is an experienced regulatory affairs professional with a career spanning over three decades in the pharmaceutical industry. Currently serving as a Global Regulatory Affairs Manager at Sobi - Swedish Orphan Biovitrum AB since May 2018, Margareta has previously held key regulatory roles, including Consultant at NDA Regulatory Service AB and Regulatory Affairs Manager at AstraZeneca R&D. Prior experience includes senior positions at Pharmacia/Pfizer, managing CMC documentation and quality assurance, as well as an early career at Apoteksbolaget. Margareta holds a B.Sc. in Dispensing Pharmacy from the University of Uppsala.