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Regulatory Anatomy: How 'Safety Logics' Structure European Transplant Medicine

机译:监管解剖学:“安全逻辑”如何构成欧洲移植医学

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This article proposes the term "safety logics" to understand attempts within the European Union (EU) to harmonize member state legislation to ensure a safe and stable supply of human biological material for transplants and transfusions. With safety logics, I refer to assemblages of discourses, legal documents, technological devices, organizational structures, and work practices aimed at minimizing risk. I use this term to reorient the analytical attention with respect to safety regulation. Instead of evaluating whether safety is achieved, the point is to explore the types of "safety" produced through these logics as well as to consider the sometimes unintended consequences of such safety work. In fact, the EU rules have been giving rise to complaints from practitioners finding the directives problematic and inadequate. In this article, I explore the problems practitioners face and why they arise. In short, I expose the regulatory anatomy of the policy landscape.
机译:本文提出了“安全逻辑”一词,以理解欧盟内为协调成员国立法以确保安全,稳定地提供用于移植和输血的人类生物材料而进行的尝试。通过安全逻辑,我指的是旨在最小化风险的各种讨论,法律文档,技术手段,组织结构和工作惯例的集合。我用这个术语来重新定向对安全法规的分析关注。而不是评估是否达到安全性,重点是探索通过这些逻辑产生的“安全性”类型,并考虑此类安全工作有时会产生意想不到的后果。实际上,欧盟规则引起了从业者的抱怨,他们发现该指令存在问题且不充分。在本文中,我将探讨从业者面临的问题以及产生这些问题的原因。简而言之,我揭示了政策格局的监管结构。

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