Elsa Grangier is a toxicologist currently serving as a non-clinical assessor at the ANSM (French Medicines Agency) and as a member of the Scientific Advice Working Party at the European Medicines Agency. They have a wealth of experience, having previously evaluated toxicological files for phytopharmaceutical products at ANSES and led the in vitro toxicology department at SEDIFA Laboratoire. Elsa holds a Doctorate in Pharmacy with a specialization in Toxicology from the Faculté de pharmacie in Lyon and obtained a Master's degree in Toxicology and Vigilance from UFR Pharmacie in Paris. Their expertise includes the assessment of toxicity studies and risk evaluation for medicinal products.
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