Fernanda Coello is a pharmaceutical biologist specializing in regulatory affairs, with over 12 years of experience in the pharmaceutical and consumer industries. Currently, they serve as the Leader of Regulatory Affairs for Latin America at Lundbeck, following roles at Procter & Gamble, Teva Pharmaceuticals, Johnson & Johnson, and Schering-Plough-MSD. Throughout their career, Fernanda has successfully managed the registration process for more than 50 products and has driven initiatives to optimize approval times in highly regulated markets. They are dedicated to shaping policies around access to innovative treatments by bridging science, public health, and advocacy.
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