Drug Development Congress
9th & 10th June 2010, le Montreux Palace, Switzerland
Drug Development Congress is administered by Osney Media.
Speakers

Our carefully researched speaker programmes are further enhanced by the opportunity for the delegates and speakers to discuss topics of interest in more detail during panel discussions. This means that the attendees not only benefit from the expertise of the high level speaker panel but also that of the other delegates.

 

If you have a cutting edge case study or a presentation and would like to join the speaker panel at the 2nd Annual Drug Development Congress, please contact Chris Davies at c.davies@oxfordglobal.co.uk

 

Speakers already confirmed for the 2010 Congress:





Wolfgang M. Baiker, Corporate Head of Development, Boehringer Ingelheim
James Bailey, GSK Team Leader, Medicinal Chemsitry, GSK
Sophie Banzet, Head of Safety Science CNS, Roche
Gabriel Bavarel, CEO Metabolys
Carles Callol Massot, Scientific Director Biobide S.L.
Mireille Cantarini, Internal Clinical genetics Expert, Astrazeneca
Annick Cauvin, Senior Principal Scientist, Toxicology, UCB
Gvido Cebers, Principal Scientist, CNSP Research Area Toxicologist, Global Safety Assessment, Astrazeneca
Dominique, Demolle, CEO, Aepodia
Martin Elmlinger, Director Biomarkers, Nycomed
Angela, Flannery Director, R&D Science Policy, Astrazeneca
Catharine Goddard, Translational Scientist, Pfizer, TMRC lab
Chris Goldring, Senior lecturer, MRC Centre for Drug Safety Science, Department of Pharmacology & Therapeutics
Guidp Hannauer, Director, Head of General and Safety Pharmacology, Nycomed GmbH
Dr. Thomas Herget, Senior Director R&D New Technology Evaluation Performance & Life Science Chemicals, Merck
Vicki Ikin, Clinical Biomarker Scientist Group Manager, Astrazeneca
Michael, L. Lim, PharmD, Oncology Medicine Development Centre,
Roy Mansfield, Director Safety and Risk Management, Pfizer
Dr. Julian C. Matthews, Senior Lecturer in the School of Cancer and Imaging Sciences, University of Manchester
Helen Mckeever, Pre-clinical Programme Manager Almac
Howard Mellor, Pre-Clinical Safety Scientist, General Toxicology Sciences, Safety Assessment UK, Astrazeneca
David Nicholson, Senior Vice President and Head, Worldwide Licensing and Knowledge Management, Merck & Co., Inc
Michael O'Connell, Director, Life Sciences, Clinical Practice, Spotfire, TIBCO Software INC.
Elke Persohn, Head of Cellular Imaging Group, Novartis
Marc Princivalle, Director of Toxicology, Research and Preclinical Development & Head of Preclinical Rish Assessment, EMEA, Stiefel (GSK)
Eugenii Rabiner, Director, Clinical Imaging Applications, GSK
Mandana Rezwan, Head R&D, Dualsystems Biotech
Tino Rossi, VP Preclinical Drug Discovery & Enabling Technologies, Neurosciences CEDD, GlaxoSmithKline
Thomas Steinbach, Senior Director Safety Surveillance & Risk Management, Wyeth
Linda Surh, Director, Global Regulatory Affairs (GRA) Discovery, GSK
Austin Tanney, Scientific Liaison Manager, Almac
Jean-Pierre Valentin, Director Safety Pharmacology AstraZeneca
Philippe Van der Auwera, Global Head of Safety, Roche
Will Watson, Senior Partnering Director, Teva Innovative ventures
Derek Zhang, Vice President of Clinical Pharmacology and Regulatory Affairs, Frontage laboratories
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