Joe De Vito, PharmD

Senior Director, Global Quality Compliance
Teva Pharmaceuticals

Dr. De Vito heads up the Global Quality Audit and Compliance group for Global Compliance with provides compliance support to the Teva Global Operations Manufacturing network, with groups in the Americas, Europe and the Asia/Pacific. Before joining the audits and compliance team, Joe led the Quality Systems team and was the Head of Quality Operations for the Teva US Manufacturing sites.
Dr. De Vito has held positions of increasing responsibility over 30 years in the generic industry which include conducting BA/BE/Clinical studies, leading generic drug development for solid and parenteral dosage forms, executing technical transfer and scale up programs and oversight of pre-approval and surveillance inspections.

Joe holds a B.S. in Pharmacy from the Albany College of Pharmacy, a Doctor of Pharmacy from the Medical University of South Carolina and a Research Fellowship in Pharmacokinetics from the State University of New York at Buffalo.

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