台湾tpp相关专利联动制度之建议分析。

Ping-hsun Chen
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引用次数: 2

摘要

跨太平洋伙伴关系协定(TPP)要求成员国实施第18.53条规定的专利联系制度。为成功加入TPP,台湾已开始立法专利联动制度,提出药事法修正案。第18.53条要求成员要么采用第1款规定的通知机制,要么停止第2款规定的上市批准的发放。但是,台湾的提议包括这两项措施。台湾的专利联动系统允许先驱制药公司注册要求(a)材料,(b)组合或配方,或(c)药物用途的专利。可能从该机制中受益的专利权人的范围比所要求的要大。此外,该系统要求仿制药公司在提交药品申请时通知专利权人,如果仿制药公司声称无效或非侵权,仿制药公司必须证明。此外,在专利权人向法院起诉仿制药公司期间,保健当局可以暂停发放仿制药许可证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of the Proposed TPP-Related Patent Linkage System in Taiwan.
The Trans-Pacific Partnership (TPP) Agreement mandates member states to implement a patent linkage system vested in Article 18.53. To successfully join the TPP Agreement, Taiwan has begun the legislation of a patent linkage system by proposing an amendment for the Pharmaceutical Affairs Act. Article 18.53 requires a member either to adopt a notification mechanism under Paragraph 1 or to stay the issuance of marketing approval under Paragraph 2. But, Taiwan's proposal includes both measures. Taiwan's patent linkage system allows a pioneer drug company to register patents claiming (a) a material, (b) a combination or formula, or (c) pharmaceutical use. The scope of patentees who may benefit from the mechanism is larger than what is required. In addition, the system requires a generic drug company to notify the patentee at the time of filing the drug application if the generic drug company asserts invalidity or non-infringement which the generic drug company must prove. Furthermore, the health authority is allowed to stay the issuance of a generic drug permit while the patentee is suing the generic drug company in the court.
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