Sara Richardson is currently the Associate Director of Clinical Regulatory Writing at AstraZeneca, where they lead regulatory submissions and ensure quality compliance. They have extensive experience in pharmaceutical drug product development, focusing on formulation and analytical development across various clinical phases. Prior to their role at AstraZeneca, Sara served as a VP of CMC & Regulatory Affairs at Stayble Therapeutics and gained valuable experience as an R&D Scientist/Product Developer at AstraTech. Sara holds both a Master's and a PhD in Chemistry from Lund University.
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