Ten Years of FDA Tobacco Regulation: Lessons for Public Health Stakeholders.

IF 0.3 4区 医学 Q3 LAW
Desmond Jenson
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引用次数: 1

Abstract

In the 10 years that the U.S. Food and Drug Administration (FDA) has been regulating tobacco products, the agency has been plagued with setbacks, some of its own making, and some the result of outside forces. What has been consistently true is that the public health community has not had as much of a voice as it should have until public health groups began filing lawsuits against the FDA. This article examines four areas of FDA regulation over the last decade in an attempt to qualitatively describe the work of the Center for Tobacco Products and identify opportunities for public health groups to have greater advocacy success in the future.

十年的FDA烟草法规:给公共卫生利益相关者的教训。
在美国食品和药物管理局(FDA)监管烟草产品的10年里,该机构一直受到挫折,有些是自己造成的,有些是外部力量的结果。一直以来的事实是,直到公共卫生组织开始对FDA提起诉讼,公共卫生界才有了应有的发言权。本文考察了过去十年中FDA法规的四个方面,试图定性地描述烟草产品中心的工作,并确定公共卫生组织在未来取得更大宣传成功的机会。
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
1.10
自引率
0.00%
发文量
3
期刊介绍: The Journal of Legal Medicine is the official quarterly publication of the American College of Legal Medicine (ACLM). Incorporated in 1960, the ACLM has among its objectives the fostering and encouragement of research and study in the field of legal medicine. The Journal of Legal Medicine is internationally circulated and includes articles and commentaries on topics of interest in legal medicine, health law and policy, professional liability, hospital law, food and drug law, medical legal research and education, the history of legal medicine, and a broad range of other related topics. Book review essays, featuring leading contributions to the field, are included in each issue.
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