Science Advisor

Svetlana Lyapustina, Ph.D. is a senior science advisor in the Government & Regulatory Affairs Practice Group and a member of the Pharmaceutical Team.

Svetlana counsels individual companies and consortia comprised of industry, government and academia representatives on a wide range of topics related to medical product development, quality control, manufacturing, regulatory compliance, patient adherence, regulatory submissions and intellectual property.  She has represented clients before the U.S. Food and Drug Administration (FDA), U.S., Japanese and European Pharmacopoeias (USP, JP and EP), Health Canada, European Medicines Agency (EMA), International Organization for Standardization (ISO) and other regulatory, governmental and scientific agencies in the United States and other world regions.  Her specialty is helping people address complex regulatory and technical problems constructively.