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首页> 外文期刊>IIC:International review of intellectual property and competition law >Extending the Limits of Protection of Pharmaceutical Patents and Data Outside the EU - Is There a Need to Rebalance?
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Extending the Limits of Protection of Pharmaceutical Patents and Data Outside the EU - Is There a Need to Rebalance?

机译:扩展对欧盟以外地区药品专利和数据保护的限制-是否需要重新平衡?

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摘要

The European Union (EU) has instituted internal and external measures aimed at protecting and enforcing intellectual property rights. In the area of pharmaceutical patents, the Union has also sought to protect its industries through patent term extension and data exclusivity. Recent EU Free Trade Agreements (FTAs) with developing countries contain chapters on intellectual property that extend patent terms and data exclusivity for pharmaceutical products. Such acts further prolong the lifespan of protection given to existing products and limit generic market entry. This article identifies the issue as one of "cross-pollination" of laws and argues that since similar laws exist in the internal regime of the EU, incorporating them into the EU would not be technically too difficult. However, to an extent this regime is simulated in developing countries, implementation will bring major difficulties to the health sector and economies of these countries. The article thus proposes that developing countries should not be forced to adopt such laws through FTAs, and if they are, there should be the compulsory inclusion of both (1) a clause on transitional arrangements for developing countries specific to intellectual property; and (2) a clause that clearly links the objectives for intellectual property protection and enforcement (in this context, patent term extension and data exclusivity) to balancing between the promotion of technological innovation and access to medicines.
机译:欧洲联盟(EU)制定了旨在保护和实施知识产权的内部和外部措施。在药品专利领域,欧盟还试图通过专利期限扩展和数据专有权来保护其行业。最近与发展中国家签订的欧盟自由贸易协定(FTA)包含有关知识产权的章节,这些章节扩展了药品的专利条款和数据专有权。此类行为进一步延长了对现有产品的保护期限,并限制了通用市场准入。本文将这个问题确定为法律的“异花授粉”之一,并指出,由于类似的法律存在于欧盟内部体系中,因此将它们纳入欧盟在技术上不会太困难。但是,在一定程度上在发展中国家模拟这种制度,实施将给这些国家的卫生部门和经济带来重大困难。因此,该条建议,不应强迫发展中国家通过自由贸易协定通过此类法律,如果有的话,则应强制将两者都包括在内。(1)关于专门针对知识产权的发展中国家的过渡安排的条款; (2)明确将知识产权保护和执法目标(在此情况下为专利术语扩展和数据专有性)与促进技术创新与获得药品之间的平衡联系起来的条款。

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