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欧盟的生物技术专利政策——以德国的发展为例。

Biotechnology patenting policy in the European Union--as exemplified by the development in Germany.

作者信息

Schrell Andreas, Bauser Herbert, Brunner Herwig

机构信息

Fraunhofer nstitue for Interfacial Engineering and Biotechnology, Stuttgart, Germany.

出版信息

Adv Biochem Eng Biotechnol. 2007;107:13-39. doi: 10.1007/10_2007_049.

Abstract

Patenting of biotechnological inventions is an important concomitant side effect of progress in this field, but also a matter of dispute in the public. In this paper, the significance of and the prerequisites for patenting are reviewed, and the principal requirements for biotechnology patents in the signatory states of the European Patent Convention (EPC) are summarized. This is followed by a report on the historical development of biotech-patent legislation in Europe and in Germany as one contracting state to EPC and member state of the European Union. Characteristic features of the patenting policy in Europe and Germany are illustrated by critical examples of biotechnology patents or patent applications. Some examples illustrate the influence of the European Union's national states' case laws after these had crystallized into the EU Biotechnology Directive (1998), which later was adopted by the European Patent Organization into its Implementing Regulations (2001) and was implemented into national patent acts. Some frequent objections against patenting in modern biotechnology are considered. More and better information about prerequisites, consequences, and opportunities of patenting in biotechnology, if conveyed to science and technology scholars as multipliers, may help to rationalize public discussion.

摘要

生物技术发明的专利申请是该领域进步带来的一个重要附带效应,但在公众中也是一个有争议的问题。本文回顾了专利申请的意义和前提条件,并总结了《欧洲专利公约》(EPC)签署国对生物技术专利的主要要求。接下来是关于欧洲以及作为EPC缔约国和欧盟成员国的德国生物技术专利立法历史发展的报告。欧洲和德国专利政策的特点通过生物技术专利或专利申请的关键实例来说明。一些例子说明了欧盟成员国的判例法在形成《欧盟生物技术指令》(1998年)后所产生的影响,该指令后来被欧洲专利组织纳入其《实施条例》(2001年)并被纳入国家专利法。文中还考虑了一些对现代生物技术专利申请的常见反对意见。如果能将关于生物技术专利申请的前提条件、后果和机会的更多更好的信息传达给作为传播者的科技学者,可能有助于使公众讨论更加理性。

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