Roberta Distefano is an experienced R&D Manager at IBSA Group since January 2021, with a strong background in regulatory affairs and clinical studies within the medical device sector. Prior roles include Regulatory Affairs Specialist and QA at NUTRILINEA S.R.L. and 1MED SA, providing regulatory support focused on borderline medical devices, as well as conducting clinical evaluations and post-market clinical follow-up in compliance with EU directives. Additional experience includes coordinating oncological clinical trials at Azienda Ospedaliera Universitaria San Martino and managing data for oncohematological clinical trials at Istituti Ospitalieri di Cremona. Roberta holds a Laurea magistrale in Biotecnologie mediche e farmaceutiche and multiple degrees from prestigious institutions, demonstrating a solid educational foundation in biological sciences.
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