Galderma
Emma Lundberg is an accomplished professional in regulatory affairs and medical device strategy, currently serving as the Head of Medical Devices Regulatory Strategy at Galderma since August 2005. Emma has held various significant positions at Galderma, including Head of Regulatory Affairs for Restylane NASHA and CMC & Compliance, as well as Regulatory Affairs Manager for CMC. Prior to joining Galderma, Emma gained valuable experience as a Laboratory Engineer at Biovitrum and Läkemedelsverket. Emma holds a Master of Science degree in Chemical Engineering from Uppsala University, obtained in 2004.
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