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Tue 06 Nov 2007
- Wed 07 Nov 2007
Corinthia Towers Hotel, Prague, Czech Republic
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This event is the one-stop-shop for all of your generics registration requirements. Register now to overcome all of the latest regulatory challenges affecting the generics industry. This is your best opportunity to hear from a wide range of national and international regulatory bodies and to benchmark your protocols against case studies from industry leaders.
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Who Will Attend?
Directors, Managers and Heads of:
Regulatory Affairs, Product Registration, Pharmacovigilance, Licensing, Business Development
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Don't Miss
Your panel of expert speakers include:
- Klaus Menges, European Regulatory Specialist, BfArM, Germany
- Gabriele Eibenstein, Head of Unit Regulatory Affairs, Federal Institute for Drugs and Medical Devices (BfArM), Germany
- Katrin Kiisk, Department of Human Medicines, State Agency of Medicines, Estonia
- Norbert Bangert, Former Generics Manager, Bayer, Germany
- Herta Pálfi Goóts, Regulatory Affairs Manager, Gedeon Richter Ltd, Czech Republic
- Jane Trevanion, Regulatory Affairs Director, Merck Generics UK Ltd, UK
- Claus Fuxen, Head of Regulatory Affairs, Siegfried Ltd, Switzerland
- Gordon Johnston, Vice President Regulatory Sciences, Generics Pharmaceutical Association (GPhA), USA
- Hernâni Sério, Director of Regulatory Affairs, Fresenius Kabi AG, Portugal
- Murat Hamzakadi, Senior Regulatory Affairs Manager - Infrastructure,
Astellas Pharma Europe BV, The Netherlands
- Andrey Mladenov, Director Medical and Regulatory affairs, Sopharma, Bulgaria
- Heinz Kobelt, Secretary General, European Association of Euro-Pharmaceutical Companies (EAEPC), Belgium
- Theo Raynor, Professor of Pharmacy Practice & Executive Chairman, LUTO Research Ltd, University of Leeds, UK
- NEW SPEAKER!!! Diana Taylor, Medical Writer and In-house Instructor, PAREXEL International GmbH, Germany
- NEW SPEAKER!!! Luke Kempton, Wragge and Co, UK
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Key Presentations
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