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Position and enforcement practice of the People’s Republic of China’s pharmaceutical data exclusivity protection

机译:中华人民共和国药品数据专有权保护的位置和执法实践

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摘要

The concept of pharmaceutical data exclusivity protection comes from the West. The Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS) establishes the basic rules for pharmaceutical data exclusivity protection. People’s Republic of China’s domestic law is consistent with the TRIPS agreement. In the drug registration approval process of the People’s Republic of China’s Drug Supervision Department, pharmaceutical data exclusivity protection has encountered some problems, including data authentication, exclusive rights to data, number of drugs requiring data to be submitted, and drug costs. In view of the long-term interests of the People’s Republic of China’s pharmaceutical industry and intellectual property protection trends, there are a lot of difficulties in the enforcement of pharmaceutical data exclusivity protection law that need to be overcome. Some measures can be taken, such as establishing a shorter data exclusivity protection period, only protecting the data submitted and relied on in the People’s Republic of China, only protecting the drugs that use new chemical components, allowing application and necessary research before the expiry of pharmaceutical data exclusivity protection period of generic drugs.
机译:药品数据排他性保护的概念来自西方。 《与贸易有关的知识产权协议》(TRIPS)确立了药品数据专有权保护的基本规则。中华人民共和国的国内法与TRIPS协议一致。在中华人民共和国药品监督管理部门的药品注册批准过程中,药品数据的排他性保护遇到了一些问题,包括数据认证,数据专有权,需要提交数据的药品数量以及药品费用。鉴于中华人民共和国制药业的长远利益和知识产权保护的趋势,在执行药品数据专有权保护法方面存在许多困难,需要克服。可以采取一些措施,例如建立更短的数据独占保护期限,仅保护中华人民共和国提交和依赖的数据,仅保护使用新化学成分的药物,允许在专利权到期之前进行应用和必要的研究。通用药品的药品数据专有权保护期。

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