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Veronica Musso is an experienced Regulatory Affairs professional with a robust background in managing pharmaceutical product submissions and post-approval maintenance. Currently serving as the Regulatory Affairs Project Manager Team Leader and Consultant at Pharma D&S since April 2016, Veronica has overseen national and international regulatory procedures. Previously, at Meda Rottapharm from May 2012 to April 2016, Veronica worked as a Regulatory Affairs Officer, focusing on various regulatory submissions. At Pfizer, from June 2010 to May 2012, responsibilities included preparing marketing regulatory applications and collaborating with cross-functional teams on regulatory matters, while earlier experience at Allergan Italy involved supporting marketing applications and performing pharmacovigilance activities. Veronica holds a 5-Year Degree in Pharmacy from Università di Pavia, completed in 2009.