FDA provides responses to FAQs on Tobacco Product User Fees
FDA issues a Draft Guidance “Tobacco Product User Fees: Responses to Frequently Asked Questions.” Starting May 27, the public may submit comments through July 26, 2021.
Q&A with CTP’s New Director of the Office of Regulations
Learn about May Nelson’s contributions to improve public health through tobacco regulation.
FDA posts list of deemed products received through the PMTA pathway
FDA posts a list of over 6 million deemed new tobacco products for which a premarket application was submitted to FDA via the Premarket Tobacco Product Application (PMTA) pathway by Sept. 9, 2020.
September 9, 2020 Premarket Review Submission Deadline
FDA created a new webpage to provide manufacturers and importers with a single location for information and resources related to tobacco product applications for deemed new tobacco products, which were due by September 9, 2020. For tips, resources, and the latest information specific to these applications, visit the new webpage.Learn More
Tobacco Education Resources for Parents and Teachers
As youth e-cigarette use remains a public health crisis, it is important that parents and educators have access to resources to learn more and to start an honest conversation with teens about the dangers of youth tobacco use. FDA has free resources available, including videos, infographics, posters, and fact sheets.Learn more
1-877-287-1373 (9am - 4pm ET)
For General Inquiries: AskCTP@fda.hhs.gov
Center for Tobacco Products
Food and Drug Administration
10903 New Hampshire Avenue
Document Control Center
Building 71, Room G335
Silver Spring, MD 20993-0002