Article 31 of the TRIPS Agreement1>
Agenda
FRIDAY - 26 MARCH 1999
Palais des Nations, Room VIII
OPENING COMMENTS (9:00 - 9:15)
James Orbinski, Canada, Chairman of Médecins Sans Frontières International
Panel I : THE NATURE OF ACCESS PROBLEMS FOR ESSENTIAL DRUGS AND MEDICAL TECHNOLOGIES (9:15 - 10:45)
Chaired by Eva Ombaka, Pharmaceutical Advisor, Churches Action International
- Bernard Pecoul, France, Médecins Sans Frontières International
- Richard Laing, USA, Associate Professor, Department of International Health, Boston University
- Jerome Dumoulin, France, Universite Pierre Mendes France, Grenoble The consequences of patents on prices, an international review..
- Eric Sawyer, USA, ACT-up New York
- Saree Aongsomwang, Thailand, Thai Consumer Foundation
Panel II : INTERNATIONAL LAW AND COMPULSORY LICENSING (11:00 - 12:30)
Chaired by Dr. Zafar Mirza, Pakustan, Coordinator, The Network, Association for Rational Use of Medication.
- Dr Adrian Otten, WTO, Director Intellectual Property Division What is compulsory licensing and what is the role of WTO in compulsory licensing?
- Prof Bernard Remiche, Belgium, Departement de droit economique et social, Universite de Louvain
- Dr. Carlos M. Correa, Argentina, Centro de Estudos Avanzados, Universidad de Buenos Aires
LUNCH (12:30 - 1:30)
Panel III : PRACTICAL ISSUES RELATING TO COMPULSORY LICENSING (1:45 - 3:15)
Chaired by Ellen't Hoen, the Netherlands, MSF, HAI
- Carlotta Graffigna, Director Advisory, WIPO, WIPO's assistance in drafting legislation on compulsory licensing.
- James Love, USA, Consumer Project on Technology Methods of determining a reasonable compensation in compulsory licensing.
- Jon F. Mertz,Center for Bioethics, University of Pennsylvania, Compulsory licensing in new medical technologies.
- Bill Hadad, USA, CEO MIR Pharmaceuticals Compulsory licensing in practice: the generic industry experience.
Panel IV : VIEWS AND PERSPECTIVES ON COMPULSORY LICENSING (3:30 - 5:15)
Chaired by Dr. Krisantha Weerasuriya, Sri Lanka, University of Colombo, Department of Pharmacology.
- Dr. Michael Scholtz, WHO, Executive Director, Health Technology and Drug Cluster.
- David Waters, USA, IFPMA, SmithKline Beecham The position of the IFPMA on compulsory licensing.
- Jim Keon, Canada, Co-Director IGPA, President CDMA The position of the generic insutry on compulsory licensing.
- Nadine Gasman, Mexico, AIS/HAI The public health implications of not granting licenses.
- Paul Toh, Thailand, GNP+/APN+/APCASO The Thai movement on compulsory licensing of pharmaceutical patents.
- Desmond Johns, South Africa, Permanent Mission in Geneva The South African experience in access to drugs and compulsory licensing.
- Invited, Lois Boland, USA, Patent and Trademarks Office The US position on compulsory licensing on the national and international levels.
- DR. K. Balasubramaniam, Malaysia, Pharmaceutical Advisor, CIROAP The consumer perspective on compulsory licensing.
CONCLUDING REMARKS (5:15 - 5:30)
Bernard Pecoul, France, Médecins Sans Frontières International
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