Regina Kumar is a regulatory professional with extensive expertise in US, EU, and international regulations for medical devices. They previously served in various roles at Abbott from 2008 to 2010, including Associate Director of Regulatory Affairs, where they managed toxicology and product labeling, and RA Manager, overseeing regulatory filings and team training. Regina's experience includes leading cross-functional teams, ensuring compliance for IVD products, and supporting product development and regulatory strategy. With a strong commitment to fostering collaborative environments, Regina aims to enhance patient care by aligning healthcare innovations with regulatory standards.
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