Regulatory Counsel

0910-AH22 201510 The Regulatory Plan and the Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Requirements for Tobacco Product Manufacturing Practice

FDA is proposing requirements that govern the methods used in, and the facilities and controls used for, the pre-production design validation, manufacture, packing, and storage of tobacco products.

]]> Economically Significant Previously Published in The Unified Agenda Proposed Rule Stage Yes Undetermined 21 CFR 1120 21 U.S.C. 371 21 U.S.C. 387b 21 U.S.C. 387f No ANPRM 03/19/2013 78 FR 16824 ANPRM Comment Period End 05/20/2013 NPRM 04/00/2016 Yes Businesses Undetermined No Yes No Darin Achilles Regulatory Counsel 0910 Food and Drug Administration FDA 877 287-1373 301 595-1426 ctpregulations@fda.hhs.gov 14-101-11, 10903 New Hampshire Avenue, Document Control Center, Building 71, Room G335, Silver Spring MD 20993