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No Longer Business as Usual: FDA Exceptionalism, Commercial Speech, and the First Amendment

机译:不再像往常一样业务:FDA异常主义,商业演讲和第一次修正案

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摘要

FDA's crucial mission of protecting the safety and integrity of our nation's food and drug supply has led to several areas of "FDA exceptionalism"-a tendency to apply available exceptions to general legal norms. Until the late 1990s, the First Amendment seemed another of these areas, and FDA was free to regulate the labeling and advertisement of products within its jurisdiction. But in the last two decades, FDA has lost case after case with respect to challenges under the First Amendment. Its response has been to strategically avoid appealing these decisions, to construe these decisions as narrowly as possible, and to attempt to continue on business as usual. This article covers the evolution of the Supreme Court's First Amendment jurisprudence as relates to FDA. It argues that commercial speech restrictions are currently subject to a de facto strict scrutiny applied under the Central Hudson name. It also covers the areas of compelled speech, compelled access, compelled subsidies, government speech, and compelled commercial disclosure, all of which will prove relevant to FDA in designing future regulatory approaches. It discusses three areas of current FDA First Amendment difficulty health claims for dietary supplements, off-label pharmaceutical promotion, and graphic cigarette warning labels and argues that FDA's current approach to addressing First Amendment concerns is unsustainable. It uses First Amendment caselaw to offer guidance on possible future approaches that would proactively address these issues and balance the First Amendment rights of regulated entities with FDA's crucial public health goals.
机译:FDA保护我们国家食品和药物供应安全性和诚信的关键使命导致了“FDA异常主义”的几个领域 - 将可用例外应用于一般法律规范的趋势。直到20世纪90年代末,第一次修正案似乎是另一个领域,FDA可以自由地规范其管辖范围内的产品的标签和广告。但在过去的二十年中,FDA在第一次修正案下的挑战方面失去了案例。它的回应是战略性地避免上诉这些决定,以尽可能狭隘地解释这些决定,并试图像往常一样继续业务。本文涵盖了最高法院首次修正案判例的演变,涉及FDA。它认为,商业言论限制目前受到在中央哈德森名称下应用的事实上的严格审查。它还涵盖了强迫演讲的领域,强迫访问,强制补贴,政府言论和推动的商业披露,所有这些都将与FDA设计有关,以设计未来的监管方法。它讨论了目前FDA第一修正案的三个领域对膳食补充剂,非标签药品促销和图形卷烟警告标签的健康索赔,并认为FDA目前解决第一次修正案的方法是不可持续的。它采用第一个修正案Quencement Caselaw提供有关未来未来方法的指导,这些方法将主动解决这些问题,并使FDA关键的公共卫生目标进行监管实体的第一个修正权利。

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