增加有效药物开发的几率:将监管事务专业人员提升为战略合作伙伴

Daniela Drago, M. Yap, O. Ekmekci
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引用次数: 2

摘要

在当今全球化的药物开发环境中,对监管专业人员更无缝地整合到战略决策中的需求是显而易见的。虽然少数公司看到了让监管事务专业人士参与战略业务决策的好处,但许多公司仍然落后。关于监管事务专业人员在产品开发、发布和生命周期管理的各个阶段的战略制定过程中是否有地位和权力做出有意义的贡献,文献和学术讨论有限。本文考察了受监管行业的当前商业环境;讨论了监管事务在这一领域发挥积极和战略性作用的重要性;并提出了一种新的教育视角,以促进对监管事务专业人员作为战略合作伙伴的认可和接受。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Increasing the odds of effective drug development: Elevating regulatory affairs professionals to strategic partners
Abstract In today’s globalized drug development landscape, the need for regulatory professionals to be more seamlessly integrated into strategic decisions is evident. Whereas a few companies see the benefit of involving regulatory affairs professionals in strategic business decisions, many still lag behind. Limited literature and scholarly discussion is available on whether regulatory affairs professionals are given the stature and power to make a meaningful contribution during strategy formulation across all stages of the product development, launch, and life-cycle management. This article examines the current business environment for the regulated industries; discusses why it is important that regulatory affairs play an active and strategic role in this sector; and proposes a new educational perspective to facilitate the recognition and acceptance of regulatory affairs professionals as strategic partners.
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