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Safeguarding access to medicines in developing countries: Strategies and principles

机译:保障发展中国家获得药品的战略和原则

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摘要

The Agreement on Trade-related Aspects of Intellectual Property Rights (TRIPS) has harmonised standards for intellectual property rights, including patents. For developing countries, these new standards are usually higher than their previous standards. As a result, it will take longer for generic versions of new drugs to enter their markets. This risks compromising access to medicines. This paper points out that developing countries can mitigate the negative impact on access by ensuring that domestic laws contain workable provisions for compulsory licensing and other TRIPS-compliant safeguard mechanisms and by gaining experience in using them. But countries should also avoid issuing trivial patents, for instance by applying strict criteria for patentability. This will, however, require a change in attitude towards and administration of intellectual property rights. Generics companies should nurture and actively support a more critical attitude to pharmaceutical patents.
机译:《与贸易有关的知识产权协定》(TRIPS)已经统一了包括专利在内的知识产权标准。对于发展中国家而言,这些新标准通常高于其先前的标准。结果,新药的仿制药进入市场需要更长的时间。这冒着损害获得药物的风险。本文指出,发展中国家可以通过确保国内法律包含关于强制许可和其他符合TRIPS的保障机制的可行规定,并获得使用经验来减轻对获取的不利影响。但是,各国也应避免发布琐碎的专利,例如通过应用严格的可专利性标准。但是,这将需要改变对知识产权的态度和管理。仿制药公司应培育并积极支持对药品专利采取更严格的态度。

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