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The presentation will begin at 1:15 pm on Monday, November 15 and will examine the storage, handling and distribution of drugs through an update on the USP general chapter .
Dr. Foster is a 28-year veteran of the pharmaceutical/biotechnology industry, with specialized expertise in the area of regulatory compliance, regulatory affairs, quality control and quality assurance roles in the manufacturing, packaging, holding and transportation of product encompassing global operations. She has worked for Catalent for 20 years at various sites and in roles of increasing responsibility within the quality and regulatory function. Today, she serves as the Vice President of Quality for Catalent working on global external relationships with worldwide regulatory agencies, pharmacopeias, academia and industry organizations in standards and guidance setting. Dr. Foster is also responsible for the global cGMP education process.
For a follow-up interview with Dr. Foster, please contact Patricia McGee at [email protected].
Dr. Foster is a 28-year veteran of the pharmaceutical/biotechnology industry, with specialized expertise in the area of regulatory compliance, regulatory affairs, quality control and quality assurance roles in the manufacturing, packaging, holding and transportation of product encompassing global operations. She has worked for Catalent for 20 years at various sites and in roles of increasing responsibility within the quality and regulatory function. Today, she serves as the Vice President of Quality for Catalent working on global external relationships with worldwide regulatory agencies, pharmacopeias, academia and industry organizations in standards and guidance setting. Dr. Foster is also responsible for the global cGMP education process.
For a follow-up interview with Dr. Foster, please contact Patricia McGee at [email protected].
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