获得疫苗的专利和其他条件

IF 0.7 Q2 LAW
Christopher Arup, Jagjit Plahe
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引用次数: 1

摘要

本文回顾了在疫情期间获得疫苗的经验。它的调查是,与医疗支出、制造能力和监管能力等其他因素或条件相比,药品专利在多大程度上阻碍或增强了获取。为了进行审查,该论文质疑了监管治理的观点,认为分散的法律多元化领域将最大限度地扩大准入。它回顾了COVID-19之前使用抗逆转录病毒药物的经验,为目前的情况提供了指导。然后,它在发明、生产、采购和分销的标题下审查了新冠肺炎疫苗的经验。审查发现,虽然专利可能会阻碍获得疫苗,但其他获得疫苗的基本条件,如独立生产能力和采购承诺,尚未建立。监管治理现在必须采取更加协调一致的方法,调动专利监管和其他关键条件来进一步获取专利。这次审查是一次收集关于这个问题的大量评论的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patents and other conditions of access to vaccines

This paper reviews the experience with access to vaccines during the pandemic. Its inquiry is the extent to which pharmaceutical patents have hindered or enhanced access when compared to other factors or conditions like health spending, manufacturing capacity, and regulatory competence. To conduct the review, the paper queries the regulatory governance perspective when it suggests a decentralised field of legal pluralism will maximise access. It recalls the pre-COVID-19 experience with antiretrovirals to provide pointers to the present situation. It then examines the experience with COVID vaccines under the headings of invention, production, procurement, and distribution. The review finds while patents may hinder access to vaccines, other, essential conditions for access, like independent manufacturing capacity and commitment to procurement, are not established. Regulatory governance must now adopt a much more concerted, coordinated approach, mobilising both patent regulation and other key conditions to further access. The review is an opportunity to gather some of the copious commentary on this issue.

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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
43
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