Implications of the Doha Declaration on the Trips Agreement and Public Health - Health Economics and Drugs Series No. 012
(2002; 56 pages) [French] [Spanish] Ver el documento en el formato PDF
Índice de contenido
Ver el documentoForeword
Ver el documentoAcknowledgements
Ver el documentoAbbreviations and acronyms
Ver el documentoExecutive summary
Ver el documentoIntroduction
Ver el documentoScope
Ver el documentoThe role of TRIPS and IPRs
Abrir esta carpeta y ver su contenidoPublic health measures
Abrir esta carpeta y ver su contenidoFlexibility in TRIPS
Cerrar esta carpetaMembers with insufficient or no manufacturing capacities
Ver el documentoAddressed problem
Cerrar esta carpetaPossible approaches
Ver el documento(a) Article 31 (f)
Ver el documento(b) Article 30
Ver el documento(c) Moratorium
Ver el documentoSafeguards
Ver el documentoCompulsory licence in the importing country
Ver el documentoEconomic feasibility
Ver el documentoLegal implementation
Ver el documentoTransfer of technology to LDCs
Ver el documentoExtension of transitional period for LDCs
Ver el documentoSpecial treatment under TRIPS
Ver el documentoLegal status of the Doha Declaration
Ver el documentoIssues not covered in the Declaration
Ver el documentoConclusions
Ver el documentoAnnex 1 - Doha Declaration on the TRIPS Agreement and Public Health
Ver el documentoAnnex 2 - Levels of development of pharmaceutical industry, by country
Ver el documentoReferences
 

(a) Article 31 (f)

Article 31 (f) prevents the granting of a compulsory licence exclusively or mainly to export to a country in need of certain medicines88.

88 It is interesting to note, however, that some developed countries provide for compulsory licences or governmental use for export without the limitation imposed by Article 31 (f). Such is the case of Article 168 of the Australian Patent Act and Article 55 (2) of the Patent Act of New Zealand, which permit exports under an agreement with a foreign country to supply products required for the defence of that country. Article 48B(d) (i) of the UK Patent Act provides for a compulsory licence in respect of a patent whose proprietor is not a WTO proprietor when the owner’s failure to licence the patent on reasonable grounds means that a market for the export a patented product made in the UK is not being supplied.

The option based on the amendment of Article 31 (f) of the TRIPS Agreement would require three steps: (a) a political decision to open the Agreement to renegotiation and an approval of the agreed modification; (b) a change in the national law of the potential exporting country in order to delete the “predominantly” requirement already incorporated in many laws, and to specify as a ground for a compulsory licence the need to address a paragraph 6 situation, and (c) the granting in the exporting country of a compulsory licence upon request of an interested party.

The first step may encounter political resistance by those countries that are reluctant to amend any part of the Agreement, because of the risk of stimulating the renegotiation of other provisions. The second step is likely to require action by national parliaments. Legislative processes are generally complex and lengthy. In addition, though domestic producers may benefit from new export opportunities, an amendment to the national compulsory licence system may be perceived as benefiting mainly the population in a foreign country, and may fail to gain sufficient political support. Finally, if the law were amended, the government would still need to exercise its power to grant a particular compulsory licence, provided that requests were made for that purpose.

Where there was a request for a compulsory licence, it would be necessary to undertake a prior negotiation on commercially reasonable terms with the patent holder, and to determine the level of royalty compensation to be paid upon issuance of a compulsory licence. Moreover, the granting authority may have to make a determination of the level of “capacity” of the importing country and of the public health need, if these conditions were required under the Article 31 (f) amendment and/or under the national law. Compulsory licence procedures, in addition, may be costly and burdensome, and may be subject to industry’s opposition and give rise to political pressures at the bilateral level.

A possible solution based on an amendment to Article 31 (f) may also provide for double compensation to be paid to the patent holder (in both the importing and exporting countries), thus increasing the cost and possibly reducing access to the products in need.

The three-step process required for the compulsory licence option may mean that a practical solution may be years away, and does not constitute an “expeditious” solution.

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Última actualización: le 3 mayo 2013