“你说番茄,我说含有β -离子酮和苯乙醛的茄属番茄”:对康涅狄格州转基因标签立法的分析。

IF 0.3 4区 医学 Q4 FOOD SCIENCE & TECHNOLOGY Food and drug law journal Pub Date : 2014-01-01
Travis Nunziato
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引用次数: 0

摘要

“你说番茄,我说茄属番茄含有β -离子酮和苯乙醛”讨论了要求对含有转基因生物的产品进行标签的重要性,重点是康涅狄格州的转基因生物标签法规,因为这是全国第一个此类法规。本文将比较康涅狄格州的法律与澳大利亚的立法,突出康涅狄格州法案的积极方面,并确定其主要弱点,即法规中的“触发条款”。第一部分将提供基因改造的概述和提供生物技术的简史。它还将简要概述联邦生物技术管理框架,并评估美国食品和药物协会在管理基因改造方面的作用。第一部分将以讨论美国公众如何表明转基因生物标签是重要的,以及应该采取的措施来结束。本文的第二部分将探讨康涅狄格州最近的立法,要求在含有转基因生物的产品上贴标签。第三部分将探讨澳大利亚要求在含有转基因生物的产品上贴标签的立法,并将澳大利亚的法律与康涅狄格州的立法进行比较。
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"You Say Tomato, I Say Solanum Lycopersicum Containing Beta-ionone and Phenylacetaldehyde": an Analysis of Connecticut's GMO Labeling Legislation.

"You Say Tomato, I Say Solanum Lycopersicum Containing Beta-ionone and Phenylacetaldehyde" discusses the importance of requiring labels on products that contain genetically modified organisms, focusing on Connecticut's GMO Labeling statutes, as it is they are the first of their kind in the nation. The article will compare Connecticut's law to the legislation found in Australia, highlighting the positive aspects of Connecticut's bill and identifying its key weaknesses, namely the "trigger clause" found in the statute. Part I will provide an overview of Genetic Modification and provide a brief history of Biotechnology. It will also provide a brief overview of the federal regulatory framework in biotechnology, as well as evaluate the United States Food and Drug Association's role of regulating genetic modification. Part I will conclude by discussing how the American public has shown that labeling GMOs is important, and something that should occur. Part II of this article will explore Connecticut's recent legislation requiring labels on products that contain GMOs. Part III will explore Australia's legislation requiring labels on products containing GMOs, comparing Australia's law to Connecticut's legislation.

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来源期刊
Food and drug law journal
Food and drug law journal 医学-食品科技
CiteScore
0.20
自引率
50.00%
发文量
0
审稿时长
>36 weeks
期刊介绍: The Food and Drug Law Journal is a peer-reviewed quarterly devoted to the analysis of legislation, regulations, court decisions, and public policies affecting industries regulated by the U.S. Food and Drug Administration (FDA) and related agencies and authorities, including the development, manufacture, marketing, and use of drugs, medical devices, biologics, food, dietary supplements, cosmetics, veterinary, tobacco, and cannabis-derived products. Building on more than 70 years of scholarly discourse, since 2015, the Journal is published in partnership with the Georgetown University Law Center and the O’Neill Institute for National & Global Health Law. All members can access the Journal online. Each member organization and most individual memberships (except for government, student, and Emeritus members) receive one subscription to the print Journal.
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