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Deborah Carangella is a Regulatory Affairs Consultant at Pharma D&S, responsible for leading technical documentation for obtaining and maintaining Marketing Authorization for medicinal products in Europe and beyond. With experience in managing drug registration processes with AIFA and international regulatory authorities, Deborah possesses strong knowledge of ICH and EMA guidelines, regulatory strategy development, and eCTD dossier submissions. Previous roles include working as a Scientific Medical Informant in various therapeutic areas, a Beauty Consultant at LloydsFarmacia, and completing internships focused on cancer research and genetics. Deborah is currently pursuing a Master's degree in Pharmaceutical Technologies and Regulatory Activities while holding a Master's degree in Medical and Pharmaceutical Biotechnology and a Bachelor's degree in Biotechnology.