Access Denied: A Review and Critique of the Patented Medicines (Notice of Compliance) Regulations

Mohamed R. Hashim
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引用次数: 1

Abstract

In Canada, proceedings brought under the Patented Medicines (Notice of Compliance) Regulations are among the most contentious. At stake is a pharmaceutical company's ability to enter a drug onto the market.Applications under the PMNOC regime involve an innovator, or brand, company pitted against a generic drug-making company, wherein the brand company seeks to prohibit the generic from releasing a generic drug until the expiry of listed patents.In practice, the Regulations create many obstacles for the release of generic drugs. This paper reviews the provisions and critically evaluates the process of obtaining approval to release a generic drug. It is submitted, the PMNOC Regulations do not provide ideal conditions for efficient patent litigation. The provisions create undesirable litigation practices and ultimately result in a loss for the Canadian people.
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拒绝获取:对《专利药品(合规通知)条例》的回顾和批评
在加拿大,根据《专利药品(遵守通知)条例》提起的诉讼是最具争议的。这关系到制药公司将药物推向市场的能力。PMNOC制度下的申请涉及创新者或品牌公司与仿制药生产公司的竞争,其中品牌公司试图禁止仿制药在所列专利到期之前发布仿制药。在实践中,《条例》为仿制药的上市设置了许多障碍。本文回顾了这些规定,并批判性地评价了获得仿制药放行批准的过程。它认为,PMNOC条例没有为有效的专利诉讼提供理想的条件。这些规定造成了不受欢迎的诉讼做法,最终导致加拿大人民的损失。
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