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Svetlana Lyapustina, Ph.D., is a Science Advisor in the Health Practice Group and a member of the group's Pharmaceutical and Medical Device Team.
Svetlana counsels individual companies and pharmaceutical consortia on a wide range of topics related to drug product development, quality control and quality assurance, pharmaceutical manufacturing, regulatory compliance, regulatory submissions and intellectual property. She has represented clients before the U.S. Food and Drug Administration, U.S. Pharmacopoeia and other regulatory and scientific agencies in the United States and internationally. Her specialty is helping people address complex regulatory and technical problems constructively. | 