Ditea Sallaku is a professional in regulatory affairs with extensive experience in the pharmaceutical sector. Currently serving as a Senior Expert in Regulatory Affairs Lifecycle Management at Dompé since October 2020, Ditea focuses on global regulatory affairs. Prior roles include Regulatory Affairs Senior Expert for the Balkan countries and Regulatory Affairs Officer at Farmacia Italiane “Mike.” Additional experience encompasses positions as an International Trade, Logistic & Regulatory Affairs Specialist at ViniPharma Medical Group and Medical Information Specialist at Edra S.p.A. Educational qualifications include a degree in Pharmaceutical Sciences and Professional Qualification from Università degli Studi di Milano.
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