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Global pharmaceutical patents after the Doha Declaration What lies in the future?

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dc.creator Erik Alsegård
dc.date 2004
dc.date.accessioned 2013-05-30T13:57:47Z
dc.date.available 2013-05-30T13:57:47Z
dc.date.issued 2013-05-30
dc.identifier http://www.law.ed.ac.uk/ahrb/script-ed/docs/doha.asp
dc.identifier http://www.doaj.org/doaj?func=openurl&genre=article&issn=17442567&date=2004&volume=1&issue=1&spage=12
dc.identifier.uri http://koha.mediu.edu.my:8181/jspui/handle/123456789/5982
dc.description The purpose of this article is to analyse how developments after the Doha Declaration went wrong; how developing countries can best be helped by IPR legislation; and whether such help can be achieved without taking away the incentives for industry to develop medicines. It is submitted that a legal framework maintaining the global protection of IPRs is needed, especially in developed countries, but that such a framework must allow for compulsory licensing in separate, regional generic markets , and must further create effective barriers for (re-)import into other countries than those targeted by the compulsory licence. This proposal would create a large market currently unused, in which pharmaceuticals could be produced and sold more cheaply, while protecting developed countries from importation of generic drugs. This way, compulsory licensing should work as a tool to promote innovation whilst also protecting public health globally.
dc.publisher AHRB Research Centre for Studies in Intellectual Property and Technology Law
dc.source SCRIPT-ed
dc.subject Doha
dc.subject acces to medicines
dc.subject patents
dc.subject pharmaceuticals
dc.title Global pharmaceutical patents after the Doha Declaration What lies in the future?


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