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Joint MHRA/DIA Excellence in Pharmacovigilance

This course is designed to provide a firm grounding in key aspects of European Clinical Pre- and Post-Marketing Safety regulatory requirements.

KEYNOTE PRESENTATION

Speaker(s)

Mick Foy

Keynote Presentation

Mick Foy

  • Deputy Director of Patient Safety Monitoring
  • Medicines and Healthcare products Regulatory Agency (MHRA), United Kingdom

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+41 61 225 51 51

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+41 61 225 51 55