Stephanie ZEDET

Stephanie ZEDET has worked in the regulatory affairs field since 2000. Stephanie began their career as a Registration Manager at Cerexagri (now UPL). In 2006, they joined Novozymes as a European Regulatory Affairs Manager, where they were responsible for writing national and European registration dossiers for microbial plant protection products, as well as for writing national registration dossiers for fertilizers. Stephanie was also responsible for coordinating regulatory projects for all product lines, budget supervision, regulatory follow-up in European countries, and coordination of consultants at national levels. In 2009, they moved to Nufarm as an EU Regulatory Affairs Specialist. From 2017 to 2020, they worked at Albaugh Europe Sarl as a Regulatory Affairs Manager and European project coordinator. In this role, they were responsible for defining the regulatory strategy and ensuring the coordination of the studies to be done, the writing of the dossier, and the follow-up after submission. Stephanie was also the budget supervisor for projects and studies in connection with allocated molecules, and monitored toxicological studies. In 2020, they were appointed Head of Regulatory Affairs Department at Bioline Agrosciences.

Stephanie Zedet obtained their Doctorate in Pharmacy and DESS in Toxicology from Universit\u00e9 Paris Cit\u00e9 in 1999. Stephanie also obtained their Doctorat de Pharmacie and DESS de Toxicologie from Facult\u00e9 de Pharmacie Universit\u00e9 Ren\u00e9 Descartes \u00e0 Paris in the field of Sceinces biologiques et pharmaceutiques, Toxicologie.