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HHS/FDA | RIN: 0910-AH44 | Publication ID: Spring 2021 |
Title: Premarket Tobacco Product Applications and Recordkeeping Requirements | |
Abstract:
This rule will establish content and format requirements to ensure that premarket tobacco product applications contain sufficient information for FDA to determine whether the marketing of a new tobacco product should be authorized. Additionally, the rule will set forth the basic procedures for premarket tobacco product application review and require applicants receiving marketing authorization to establish records and make postmarket reports to FDA. The rule will also require tobacco product manufacturers to keep records to support legal marketing of certain tobacco products, such as documents showing that a tobacco product does not need to undergo premarket review. |
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Agency: Department of Health and Human Services(HHS) | Priority: Other Significant |
RIN Status: Previously published in the Unified Agenda | Agenda Stage of Rulemaking: Final Rule Stage |
Major: No | Unfunded Mandates: No |
CFR Citation: 21 CFR 1114 21 CFR 1100.200 21 CFR 1107.3 | |
Legal Authority: 21 U.S.C. 371 21 U.S.C. 387a 21 U.S.C. 387b 21 U.S.C. 387i 21 U.S.C. 387j 21 U.S.C. 374 ... |
Legal Deadline:
None |
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Timetable:
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Regulatory Flexibility Analysis Required: Undetermined | Government Levels Affected: None |
Federalism: No | |
Included in the Regulatory Plan: No | |
RIN Data Printed in the FR: No | |
Agency Contact: Paul Hart Senior Regulatory Counsel Department of Health and Human Services Food and Drug Administration Center for Tobacco Products, 10903 New Hampshire Avenue, Document Control Center, Building 71, Room G335, Silver Spring, MD 20993 Phone:301 796-3894 Email: ctpregulations@fda.hhs.gov |