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November 9-11, 2020 | Virtual Conference
Joyce has over 30 years of experience in the pharmaceutical industry, primarily in the generic sector, having started out in the analytical laboratory (Research and Development as well as Quality Control) and then moving into Regulatory Affairs. Now working with Teva Pharmaceuticals Inc., USA as a Sr. Director, Regulatory Affairs, she is responsible for regulatory launch execution, labeling and drug listing, and certain post approval submissions. Her past responsibilities included regulatory strategy, submission and maintenance of FDA submissions developed both internally and externally. She has experience with a variety of dosage forms, including solid oral dose immediate and extended release, sterile injectables, nasal sprays, sterile ophthalmic, creams, liquids, ointments, drug device combos and complex drug products. Joyce is a graduate of the state University of New York at Stony Brook with a Bachelor of Science degree in Biology.