Network for Monitoring the Impact of Globalization and TRIPS on Access to Medicines, Meeting Report, 19-21 February 2001, Chulalongkorn University, Bangkok, Thailand - Health Economics and Drugs Series No. 011
(2002; 67 pages) Ver el documento en el formato PDF
Índice de contenido
Abrir esta carpeta y ver su contenido1. Introduction
Ver el documento2. Highlights of opening address of Dr Supachai Panitchpakdi
Cerrar esta carpeta3. 1Globalization, TRIPS and Access to Pharmaceuticals
Ver el documentoA new era in global trade
Ver el documentoWTO Agreements
Ver el documentoImplementation and dispute settlement
Cerrar esta carpetaKey requirements of the TRIPS Agreement
Ver el documentoPatent protection
Ver el documentoRights conferred
Ver el documentoTransitional arrangements
Ver el documentoPublic health and TRIPS
Ver el documentoPatentability
Ver el documentoGeneric drugs
Ver el documentoCompulsory licensing
Ver el documentoParallel imports
Ver el documentoTRIPS-plus provisions
Ver el documentoNon-WTO Members
Ver el documentoEvaluating impacts of trade agreements
Abrir esta carpeta y ver su contenidoWHO Perspectives on Access to Drugs
Ver el documento4. Further Reading
Ver el documento5. Template of selected model indicators for studying the impact of globalization and TRIPS on access to medicines
Abrir esta carpeta y ver su contenido6. Selected indicators for studying the impact of globalization and TRIPS on access to medicines
Ver el documento7. The Collaborating Centres
 

Key requirements of the TRIPS Agreement

The TRIPS Agreement introduced global minimum standards for protecting and enforcing nearly all forms of intellectual property rights, including those for pharmaceuticals. The Agreement’s 73 Articles cover basic principles, standards and use of patents, enforcement, dispute settlement and a range of other subjects. The key requirements for pharmaceuticals are described below and summarized in Box 2.

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Última actualización: le 24 abril 2012