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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.

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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