Consumers or Patients? Medical Device Recipients under Australian Law Straddle Two Worlds.

IF 0.6 Q2 LAW Journal of Law and Medicine Pub Date : 2023-12-01
Julia Symons, Marco Rizzi
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引用次数: 0

Abstract

This article analyses the status of medical device recipients under Australian law. The 2021 Gill v Ethicon Sàrl litigation in the Federal Court of Australia has brought the issue to the fore. Moving from the Court's findings, the article dissects the specific vulnerability of medical device recipients and explores the under-researched distinction between patients and consumers under Australian law. The analysis spans the regulatory landscape for medical devices prior to marketing approval, the statutory protections and causes of actions available to consumers under the Australian Consumer Law, and the safeguards for patients developed under medical law (particularly medical negligence). In addition to doctrinal clarifications, the article provides a discussion of key policy considerations that frame the various regimes. Patients and consumers share characteristics, but their legal protections differ in terms of focus and objectives. Medical device recipients straddle both worlds, requiring the highest levels of care and disclosure.

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消费者还是患者?澳大利亚法律下的医疗器械接受者横跨两个世界。
本文分析了澳大利亚法律中医疗器械接受者的地位。澳大利亚联邦法院在 2021 年审理的 Gill 诉 Ethicon Sàrl 案将这一问题推到了风口浪尖。文章从法院的调查结果出发,剖析了医疗器械接受者的特殊脆弱性,并探讨了澳大利亚法律中患者与消费者之间研究不足的区别。文章分析了医疗器械在获准上市前的监管情况、《澳大利亚消费者法》规定的法定保护措施和消费者可提起诉讼的原因,以及根据医疗法(特别是医疗过失)制定的患者保障措施。除理论澄清外,文章还讨论了构建各种制度的关键政策因素。患者和消费者有共同的特点,但其法律保护的重点和目标却各不相同。医疗器械接受者横跨两个世界,需要最高水平的关怀和披露。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
63
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