Speakers
Hugo Stephenson, President, Quintiles Strategic Research Services
Christopher-Paul Milne, Associate Director, Tufts Centre for the Study of Drug Development
Osamu Doi, Chief Executive, Society of Japanese Pharmacopoeia
Vicki Edwards, Director, European Pharmacovigilance, Abbott Laboratories
Sabina Straus, Head of Drug Safety Department, Medicines Evaluation Board, The Netherlands
Charles Beasley, Chief Scientific Officer Global Product Safety, Eli Lilly
Juhanna Idänpään-Heikkilä, Senior Adviser, CIOMS c/o WHO
Tjeerd Van Staa, GPRD, MHRA
Carmen Bozic, VP Drug Safety and Risk Management, Biogen Idec
John Ferguson, VP Global Head of Pharmacovigilence and Medical Safety, Novartis
Songlin Xue, VP Global Head of Epidemiology, Novartis
Shelly Ghandi, Pharmacovigilance Information Unit Manager, MHRA
Guy Pawson, Manager Electronic Submissions, Genentech
Phil Berry, Global Medicines Director, Reckitt Benckiser
John Balian, SVP Global Pharmacovigilance and Epidemiology, Bristol-Myers Squibb
Michael Bone, Association of Research Ethics Committees
Dr John Talbot, Director, Clinical Drug Safety an, Processes and Standards, AstraZeneca R&D
Vivianne Arencibia, Global Head Compliance and Audit, Group Quality Operations, Novartis
Magda Daudin, Head of Pharmacovigilance Inspections, Afssaps
Stewart Jessamine, Interim Manager, Medsafe, New Zealand
Georg Ferber, Group Head Biostatistics Cardiovascular, Novartis
Katia Yamasaki, Pharmacovigilance Manager, Stiefel R&D Latin America
Kasia Petchel MD, VP & Global Head Safety Risk Management, Roche
Dana Bagan, Head of Drug Safety, GlaxoSmithKline
William Maier, Senior Director Epidemiology, Elan Pharma Ltd