Sabrina Vullo, PhD, is a Senior QA/RA Specialist at Abionic, specializing in regulatory affairs for in vitro medical devices. They graduated with a PhD in Life Sciences and possess strong experience in the management of scientific projects. Previously, Sabrina worked as a Regulatory Affairs Specialist at Bien-Air Medical Technologies, where they successfully navigated MDR audits and managed regulatory submissions. With a solid background in medical biology and a passion for science, they also have extensive scientific writing experience and are fluent in English, French, and Italian.
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