药物研发中公私合作的法律框架》。

Q1 Pharmacology, Toxicology and Pharmaceutics
Thomas Hirse
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引用次数: 0

摘要

药物研发领域的公私合作伙伴关系具有推动创新的巨大潜力。它们可以在卓越的基础研发和创新药物的商业化之间架起桥梁,以满足治疗严重疾病的未满足需求,造福公众健康和人类福祉。因此,药品研发领域的公私合作得到了各国政府和欧盟委员会的推动和公共资助。尽管如此,它们仍需遵守法律要求,特别是国家援助法和竞争法的要求。这些要求不仅要保护公平竞争,还要促进公开的信息交流,公平分担风险,公平分享收益和成果,以实现成功合作的目标,增加药品创新成功商业化的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Legal Framework for Public-Private Partnerships in Drug R&D.

Public-private partnerships in drug R&D have great potential for driving innovation. They can bridge between excellent fundamental research and development and commercialization of innovative medicines to address unmet needs for the therapy of severe diseases in the interest of public health and human welfare. Therefore, public-private partnerships in drug R&D are promoted and publicly funded by governments and the European Commission. Nonetheless, they need to comply with legal requirements, particularly stemming from State aid law and competition law. Those requirements do not only protect a fair competition, but rather also further open information exchange as well as fair sharing of risks and fair participation in gains and results with the goal of having a successful collaboration and increasing the chance of successful commercialization of pharmaceutical innovations.

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来源期刊
Handbook of experimental pharmacology
Handbook of experimental pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.20
自引率
0.00%
发文量
54
期刊介绍: The Handbook of Experimental Pharmacology is one of the most authoritative and influential book series in pharmacology. It provides critical and comprehensive discussions of the most significant areas of pharmacological research, written by leading international authorities. Each volume in the series represents the most informative and contemporary account of its subject available, making it an unrivalled reference source.
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