The Center for Tobacco Products (CTP)[1] was established by the United States Food and Drug Administration as a result of the Family Smoking Prevention and Tobacco Control Act[2] signed by President Obama in June 2009. The FDA center was responsible for the implementation of the Family Smoking Prevention and Tobacco Control Act.
The smoking prevention and tobacco law established regulatory controls for tobacco products:[3]
- Setting performance standards for tobacco products
- Reviewing premarket applications for new and modified risk of tobacco product
- Requirement of warning labels for tobacco products
- Enforcing advertising and promotion restrictions for tobacco products
The U.S. mandated legislation was a historic milestone for the U.S. FDA. The enacted law used to assist with the federal agency regulatory efforts and initiatives to curb the suspected health hazards for tobacco products on an annual basis.
YouTube Encyclopedic
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FDA Center for Tobacco Products -- Our Goal
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FDA Center for Tobacco Products -- Harmful and Potentially Harmful Constituents Announcement
Transcription
The goal of the Center for Tobacco Products is to regulate tobacco, manufacturing, marketing and distribution so that the disease and death caused by tobacco in this country is part of America’s past, not America’s future.
See also
- Little Lungs in a Great Big World, public service announcement series that is part of a campaign for the CTP
References
- ^ "About U.S. FDA Center for Tobacco Products". Food and Drug Administration. Archived from the original on 2019-04-22. Retrieved 2019-12-16.
- ^ "Family Smoking Prevention and Tobacco Control Act (Public Law 111-31)" (PDF). Archived (PDF) from the original on 2011-10-16. Retrieved 2011-09-20.
- ^ "U.S. FDA Tobacco Products Information". Food and Drug Administration. Archived from the original on 2017-11-01. Retrieved 2019-12-16.
External links
- Official website
- Tobacco Products at FDA.gov
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This page was last edited on 21 May 2024, at 07:30