© 2004 BMJ Publishing Group Ltd
Debate
FDA REGULATION
FDA REGULATION
Opposition in search of a rationale: the case for Food and Drug Administration regulation
Correspondence to:
Correspondence to:
Matthew L Myers
mmyers@TobaccoFreeKids.org
Keywords: Food and Drug Administration; FDA
| The first 150 words of the full text of this article appear below. |
For more than a decade, public health leaders have called for government regulation of tobacco products. The consensus in support of government regulation recognised that, absent strong new governmental authority, the tobacco industry would continue to do the following: pursue marketing practices that are deceptive, have a negative impact on children and discourage quitting; withhold information vital to public health scientists; secretly manipulate their products in ways that make them more dangerous and more addictive; market products that the public perceives to be less hazardous while having no incentive to market products that, in fact, deliver fewer toxins; and undermine prevention efforts by using unsubstantiated claims, such as "light" or "low tar", to keep people smoking.
To address these concerns, in May 2004 long time public health champions Senators Edward Kennedy and Mike DeWine and Congressman Henry Waxman introduced in the US Congress legislation granting the US Food
This article has been cited by other articles:
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Studlar, D. T.
(2006). Unfiltered: Conflicts over Tobacco Policy and Public Health; Smoke in Their Eyes: Lessons in Movement Leadership from the Tobacco Wars; The Fight Against Big Tobacco: The Movement, the State, and the Public's Health. Journal of Health Politics, Policy and Law
31: 395-407
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