制药法与专利法

Carlo A. Piria
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引用次数: 0

摘要

专利法和制药法律法规需要协调。提交人的解释性建议是,旨在保护作为医药产品的发明的专利权利要求必须使用有关工业医药产品的法律法规规定的适当术语来表达,如“医药产品”和“活性物质”;否则,该专利可能不被视为涵盖“医药产品”或“活性物质”。此外,因此,专利权利要求中的产品作为医药产品或活性物质的陈述意味着,该权利要求的可执行性取决于通过主管当局制备和批准药理学和临床试验档案来证明该产品的有效性和安全性。提交人所考虑的法律制度是欧洲的法律制度,但该解释性建议经必要修改后适用于其他法律制度。
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Pharmaceutical Law and Patent Law
The patent law and pharma laws and regulations need to be coordinated. The interpretative proposal of the author is that a patent claim aiming at protecting the invention as a medicinal product must necessarily be expressed using the appropriate terms provided for by the laws and regulations concerning the industrial medicinal product, such as “medicinal product” and “active substance”; otherwise the patent may not be considered as covering a “medicinal product” or an “active substance”. Moreover, as a consequence, the presentation of a product in a patent claim as a medicinal product or an active substance implies that the enforceability of such claim is conditioned upon the demonstration of the efficacy and safety of the product through the preparation and approval by the competent authorities of a dossier of pharmacological and clinical trials. The legal system taken into consideration by the author is the European one, but the interpretative proposal is, mutatis mutandis, applicable to other systems of law.
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