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Sheraton Philadelphia University City

14 oct 2019 7:45 a.m. - 16 oct 2019 4:00 p.m.

3549 Chestnut Street, Philadelphia, PA 19104

Drug Safety and Pharmacovigilance Across the Product Lifecycle

Build a solid foundation in the key concepts of drug safety and pharmacovigilance throughout the medical product development lifecycle. Learn how to comply with regulatory requirements.

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Session 22: Safety Data Coding

Session Chair(s)

Jill W. Buckley, PharmD

Jill W. Buckley, PharmD

Adjunct Assistant Professor

Rutgers, the State University of New Jersey, United States

This session will focus on the use of MedDRA for coding of adverse events. Other dictionaries used in drug safety (WHO Drug Dictionary and EudraVigilance Medicinal Product Dictionary) will be introduced.

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