Daniel Levy

Daniel Levy, PharmD, MBA, is an experienced Senior Regulatory Affairs Professional, currently serving as a Regulatory Affairs Senior Manager for Submission Management at AbbVie. With a robust history in the pharmaceutical and medical devices industry, they have developed expertise in various areas, including biotechnology, vaccines, and worldwide regulatory requirements, particularly concerning U.S. FDA and European Medicines Agency regulations. Daniel earned a Bachelor’s degree in Pharmacy from Universidade de Santo Amaro, a specialization in Business Management with an emphasis on the pharmaceutical market, and is pursuing an MBA focused on Business Process Management at FIAP. Their prior roles include significant responsibilities at prominent companies such as Johnson & Johnson and Sanofi, where they managed regulatory strategies and compliance for diverse product portfolios.