How does the regulation of tobacco products differ from FDA’s regulation of drugs or medical devices?
FDA's regulatory role for drugs and devices is usually based on a safety and effectiveness standard. The tobacco control act establishes a new standard: to regulate tobacco products based on a public health and population health standard.
- What Should I Do If I See Violations of FDA’s Tobacco Products Rules?
- FDA Center for Tobacco Products Inaugural Year and Looking Forward
- What are FDA’s Regulations for Flavored Tobacco?
- What are the new Regulations Restricting the Sale and Distribution of Cigarettes and Smokeless Tobacco to Protect Children and Adolescents?
- What will FDA do to curb tobacco use among children and adolescents?
- What are some of the key regulatory timelines associated with the tobacco control act?
- How does the regulation of tobacco products differ from FDA’s regulation of drugs or medical devices?
- Is FDA going to ban tobacco?
- What products are not considered to be tobacco products as defined by the tobacco control act?
- What products are considered to be tobacco products as defined by the tobacco control act?
- What is the main goal in regulating tobacco products?
- What are the priorities of the Center for Tobacco Products?
- Does FDA have the authority to regulate tobacco products?
- FDA Basic Video: Lawrence Deyton Discusses Tobacco (Video)
- What part of FDA regulates tobacco products?
- FDA Basics Webinar: State Enforcement Program
- How does FDA plan to enforce the restrictions on promotion and advertising established by the Tobacco Control Act?
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