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Excellence in Pharmacovigilance: Clinical Trials and Post-Marketing


Overview

This course is designed to provide a firm grounding in key aspects of European Clinical Pre- and Post-Marketing Safety regulatory requirements. This five-day training course also includes highlights and updates on the pharmacovigilance legislation and the latest news on the international harmonisation and standardisation activities in pharmacovigilance.

Program Committee

  • Gaby L. Danan, MD, PhD
    Gaby L. Danan, MD, PhD Pharmacovigilance Expert
    France
  • Phil  Tregunno
    Phil Tregunno Signal Management Unit Manager
    Medicines and Healthcare products Regulatory Agency (MHRA), United Kingdom
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