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Program Committee

  • Peter  De Veene, MD
    Peter De Veene, MD Executive Director, Clinical Safety and Pharmacovigilance Daiichi Sankyo Pharmaceuticals, United Kingdom
  • Margaret Anne Walters
    Margaret Anne Walters Director & Deputy EU Qualified Person for Pharmacovigilance Merck Sharp & Dohme Ltd., United Kingdom
  • Elspeth  McIntosh
    Elspeth McIntosh Director Castle Pharmacovigilance Ltd, United Kingdom
  • Doris Irene Stenver, MD, MPA
    Doris Irene Stenver, MD, MPA Chief Medical Officer Danish Health and Medicines Authority, Denmark
  • Vicki  Edwards, RPh
    Vicki Edwards, RPh QPPV and Head of Affiliate Vigilance Excellence AbbVie Ltd., United Kingdom
  • Michael  Richardson, MD, FFPM
    Michael Richardson, MD, FFPM International Head GPV&E and EU QPPV Bristol-Myers Squibb, United Kingdom
  • Brian David Edwards, MD, MRCP
    Brian David Edwards, MD, MRCP Principal Consultant, Pharmacovigilance and Drug Safety NDA Group, United Kingdom
  • Natalia  Kocankova, MD, MBA
    Natalia Kocankova, MD, MBA Head of Pharmacovigilance Boehringer Ingelheim RCV GmbH & Co KG , Austria
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