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India's trade-related aspects of Intellectual Property Rights compliant pharmaceutical patent laws: what lessons for India and other developing countries?

机译:印度与贸易有关的领域,符合知识产权的药品专利法:对印度和其他发展中国家有什么启示?

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摘要

India's trade-related aspects of Intellectual Property Rights (TRIPS) compliant Patent (Amendment) Act 2005 saw the transformation of its laws from a process patent regime to a product patent regime. The amendments have had a direct impact on India's generic drugs manufacturing sector, which was developed through the process patent regime introduced under the 1970 Act. The knock-on effect will soon be felt both domestically and globally, as a number of developing countries have come to rely strongly on Indian genetics. This article seeks to study the effectiveness of the Act of 2005, and if it can be seen as an instance of success of the TRIPS provisions in Articles 7 and 8 read along with the Doha Declaration. It will be queried if developing countries in the World Trade Organization can possibly benefit from the model set-up by India for the issuance of compulsory licenses, and to check the practice of 'evergreening' by pharmaceutical patent holders. Recent decisions from the Indian judiciary and the quasi-judicial authorities, along with the procedures and policies put in place will be used to carry out the study.
机译:印度在与贸易相关的《与知识产权(TRIPS)兼容的专利法》(2005年)中看到了其法律从过程专利制度到产品专利制度的转变。这些修正案直接影响了印度的非专利药品制造部门,该部门是通过根据1970年法案引入的工艺专利制度发展起来的。由于许多发展中国家已经强烈依赖印度遗传资源,因此在国内和全球都将很快感受到连锁反应。本文旨在研究《 2005年法案》的有效性,是否可以将其视为与《多哈宣言》一并解读的第7条和第8条中《 TRIPS协议》条款取得成功的实例。将询问世界贸易组织中的发展中国家是否可以从印度为强制性许可证颁发而建立的模式中受益,并检查药品专利持有人“常绿”的做法。印度司法机构和准司法当局的最新决定以及已制定的程序和政策将用于开展研究。

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