Because of the growing complexity and sophistication of the drug products our companies manufacture, regulatory authorities around the world
have been challenged to continue expanding the requirements for marketing safe and effective products. These trends have impelled companies
to put greater emphasis, and at an earlier stage, on developing an effective regulatory strategy for bringing new products to the marketplace and keeping them there. This situation has shined a new light on the importance of the skills of the regulatory team member as a key player in the development process.
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Associate Director of Pharmacy / Instructor - College of Medicine - Stony Brook Unive
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QA Compliance Auditor
Professor, TAPMI