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A UL EduNeering course

This course reviews the history and evolution of drug safety. An exploration of US pharmacovigilance, this course introduces learners to the regulatory requirements in the clinical trial and post-marketing environments and to international drug safety monitoring efforts.

Featured topics

  • History and evolution of drug safety in the United States
  • Developments in drug safety monitoring and adverse event reporting
  • Drug safety monitoring efforts in the nonclinical trial environment
  • Clinical reports
  • Postmarketing
  • Postmarketing reports
  • International safety

Who should attend?

Professionals and experts in the pharmaceutical, biotechnology, and medical device fields

Contact us

Linda Belmont, DIA
Phone +