Sarah Hood Hagberg is a seasoned professional in regulatory affairs, currently serving as a Regulatory Affairs Manager at Vitrolife since August 2011. Prior experience includes a similar role at Pharmacure and a significant tenure at AstraZeneca as a Senior Patient Safety Specialist, where responsibilities included the preparation and reporting of serious adverse events and regulatory documentation for clinical studies. Sarah also held a position as Associate Regulatory Affairs Manager at Hässle Läkemedel AB, focusing on line extensions and labelling. Educationally, Sarah holds a Master of Science in Pharmacy from Uppsala University, completed in 1996.
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