Patrizia Zanassi is a highly experienced Regulatory Affairs professional who has worked in various roles within the pharmaceutical industry. With a background in pharmacology and toxicology, Patrizia has managed regulatory activities for pharmaceutical products and medical devices, ensuring compliance with local and international regulations. Additionally, Patrizia has conducted research in neuropharmacology and has experience in quality control laboratory analysis. Their expertise spans across different companies and roles, making their a valuable asset in the industry.
January, 2023 - present
May, 2021
Regulatory Affairs Project Manager at Recordati Rare Diseases
Senior Regulatory Affairs Project Manager at Biomapas
Regulatory Affairs Project Manager at Synthon
Regulatory Affairs Project Manager at Dexcel Pharma
International Regulatory Affairs Project Manager at Recordati Rare Diseases
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