Antoine Guyot

Antoine Guyot is an experienced regulatory affairs professional with extensive expertise in the pharmaceutical industry. Currently serving as MAA Dossiers Manager in the Quality Section at Ceva Santé Animale since March 2018, Antoine oversees the quality aspects of marketing authorization applications (MAAs) for new chemical drug products across multiple regions including the EU, EMEA, LATAM, ASIAPAC, and North America. Prior roles include CMC Manager at Ceva, and Senior Regulatory Scientist at Voisin Consulting Life Sciences, where Antoine managed clinical trial activities and authored critical regulatory documents. With earlier positions at Quintiles, Real Regulatory Ltd, Ellipse Pharmaceuticals, GALENIX, and LCO Santé, Antoine has developed a strong foundation in regulatory processes, dossier preparation, and team management. Antoine holds a Doctor of Pharmacy (Pharm.D.) from Université de Bordeaux and an Inter-university degree in Volunteer Fireman Pharmacist from Université de Limoges.