Nadine is a former FDA Regulatory Scientist and Project Manager. She has over 10 years of experience with FDA regulated products, including drugs, biologicals, combination products, and food ingredients. She is a Regulatory and Medical Science Professional with clinical research and pharmaceutical experience. Additionally, Nadine’s areas of expertise also include regulatory body, key opinion leader, and stakeholder engagement; regulatory, and business planning; technical data organization and analysis; and written and verbal communication and presentation. Nadine continues to write scientific commentaries and review biomedical research manuscripts and abstracts submitted to scientific journals. Her Ph.D. and M.S. are in Medical Science from the University of South Florida College of Medicine and her Master of Public Heath (MPH) is from Johns Hopkins Bloomberg School of Public Health.