Tobacco use is the leading cause of preventable death and disease
in the United States. In 2009, the Family Smoking Prevention and
Tobacco Control Act (Tobacco Control Act) granted FDA, an agency
within the Department of Health and Human Services (HHS), authority
to regulate tobacco products, including marketing and distribution
to youth. The act established CTP, which implements the act by
educating the public on the dangers of tobacco use; developing the
science needed for tobacco regulation; and developing and enforcing
regulations on the manufacture, marketing, and distribution of
tobacco products. The act authorized FDA to assess and collect user
fees from tobacco manufacturers and importers. This book examines
how FDA spent tobacco user fees for key activities using its
authorities granted in the act, and any challenges FDA encountered
in using its authorities.
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