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UNIVERSITE LIBRE DE BRUXELLES (ULB), Belgium, Brussels
from 24 May to 28 May 2004
Drug registration : national and european procedures, european regulation on orphan medicinal products
Drug registration : the international environment
Preparation of a new drug application
Writing expert reports
Medical submission of new drug applications
Medical information
Ethics in the pharmaceutical industry
Medical databases & prescribing modules
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Organized by:
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Prof. J-M BOEYNAEMS & Mrs B. JELLOULI |
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Invited Speakers:
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Stéphane CALLEWEART, EFPIA
Francis de HALLEUX, Schering-Plough
Michel DELEERS, UCB Pharma
Lode DEWULF, Schering-Plough
Isabelle de ZEGHERS, UCB PHARMA
Frans GOSSELINCKX, Senior Lecturer at the UIA
Anne HEPBURN, GlaxoSmithKline Biologicals
André LHOIR, Ministry of Public Health
Arié KUPPERBERG, Bristol-Myers Squibb
Michèle SANGELEER, Eli-Lilly
André VANDENBERGHE, University Hospital of Charleroi
Robert H. VANDER STICHELE, Heymans Institute of Pharmacology and Belgian Health Care Council
René VAN ESSCHE, Expert of the European Union
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Deadline for Abstracts:
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no deadline
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Registration:
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You can fill the form on our web site
http://medinfo.ulb.ac.be/pharmed
700 Euro for this seminar (including access to the electronic documentation)
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E-mail:
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pharmed@ulb.ac.be
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