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Video instructions and help with filling out and completing 19 cfr importer of record
Oh are you a domestic importer of tobacco products with questions about FDA's regulations stay tuned for some answers and tips on this edition of FDA's tobacco compliance webinars Music Applause Applause Music welcome to FDA's tobacco compliance webinar education and information for retailers and small businesses sponsored by the US Food and Drug Administration and the Center for tobacco products I'm David erasing thanks for joining us today we received many questions from domestic importers of tobacco products about FDA's regulations as we've done in the past we'll be answering some of those questions today and give importers some additional tips on how to comply with the regulations joining me today is my colleague and at Christina Peters from CTP s office of compliance and enforcement you'll notice that some of the slides have links to relevant guidance documents letters and past webinars that can be found on FDA's website we encourage you to review those materials in addition to today's webinar now let's get started commander Peters thanks captain Racine the purpose of this webinar is to answer some questions we are frequently asked by importers of tobacco products and to provide some tips that we think may be helpful to importers for importers who have not seen our 2016 imports webinar we strongly encourage you to watch that webinar as well although some of the deadlines for meeting certain requirements have changed since that video was made available the topics we will be discussing today include an update on the dates to meet certain requirements which have been revised the automated commercial environment also known as ace and which data elements are and are not required when importing a regulated tobacco product establishment registration importation of regulated tobacco products for personal use prior notice for the importation of regulated tobacco products product codes tariff classification and HTS codes and user fees as we previously mentioned some compliance dates provided in the 2016 imports webinar have changed compliance dates which were presented in the 2016 imports webinar and have since changed include the compliance States for ingredient listing submissions for deemed products the compliance dates for harmful and potentially harmful constituents or H PhD submissions for deemed products the compliance dates for addictiveness warning statements on packaging and advertising for covered tobacco products other than cigars and those that do not contain nicotine the compliance state for required label statements on deemed products in package form and the compliance date for submission of applications for premarket review for deemed products on the market as of August 8th 2016 you can see the new compliance dates for these requirements across the next few slides Music the automated commercial environment or ace is the primary system through which the trade community reports imports and exports and the government determines admissibility ace is maintained by Customs and Border Protection when an FDA regulated product is imported CBP forwards the data to FDA the FDA published a final rule submission of