FDA's Center for Tobacco Products invites you to watch the new Tobacco Compliance Webinar

New Webinar Available: Tobacco Registration and Product Listing Updates FDA's Center for Tobacco Products invites you to watch the new Tobacco Compliance Webinar, "Tobacco Registration and Product Listing Updates." This webinar provides a brief overview of section 905 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), which describes the establishment registration and product listing requirements for tobacco product manufacturers. Additionally, the webinar demonstrates the new Tobacco Registration and Listing Module - Next Generation (TRLM NG), which manufacturers can use to submit the required information to the FDA. By Dec. 31 of each year, tobacco product manufacturers use FDA's Tobacco Registration and Listing Module - Next Generation (TRLM NG) to fulfill certain registration and listing requirements. Twice each year – by June 30 and Dec. 31 – all registered domestic tobacco manufacturers are required to update their product listings if they have made certain changes. Paper forms (FDA Form 3741 or FDA Form 3741a) must be mailed to CTP's Document Control Center. Visit the FDA website to see more Tobacco Compliance Webinars. Watch the New Webinar

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