Addressing the key challenges for drug safety professionals

The regulatory environment is fast changing and the drug safety industry is facing significant hurdles in implementing standards globally. It is becoming increasingly challenging to meet all regulatory requirements effectively in the current globalised marketplace. Stay on top of pharmacovigilance requirements with updates directly from the regulators, agencies and industry who will show you how to implement regulatory standards globally.

Learn from:

  • Dr Shigeki Tsuda, Senior Managing Director, Pharmaceutical and Medical Device Regulatory Science Society of Japan (PMRJ)
  • Rebecca Webb, Senior Pharmacovigilance Inspector, MHRA
  • Berit Nautrup Andersen, QPPV Senior Director, Merck Serono
  • Betina Østergaard Eriksen, Deputy QPPV, Novo Nordisk
  • Tanja Peters, Head PV Intelligence & Deputy EU-QPPV, Boehringer-Ingelheim
  • Phil Tregunno, Signal Management and Quality Standards Unit Manager, MHRA

Meet patients, physicians, pharma and health authorities to discuss effective drug safety strategies at World Drug Safety EU Congress 2015

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Finding this interesting? You might be interested in Drug Safety USA 2016 Congress. Find out more HERE