Ana Catarina Costa is a USA-Canada Post-Approval Regulatory Affairs Manager at Hikma Pharmaceuticals since January 2021, overseeing regulatory affairs for product registration and lifecycle management in the USA and Canada. With a Master's degree in Pharmaceutical Sciences from the University of Coimbra, Ana has held various roles within Hikma Farmacêutica, including USA Regulatory Affairs Supervisor and USA Regulatory Affairs Officer, where responsibilities included team management, new drug application submissions, and post-approval product management. Prior experience includes trainee positions in pharmaceutical settings, focusing on laboratory knowledge and pharmaceutical services.
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