Notices. Notice
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/register/2017/05/25/2017-10711A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
BILLING CODE 4164-01-P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket Nos. FDA-2013-N-1423; FDA-2013-N-0730; FDA-2012-N-0977; FDA-2013-N-0557; FDA-2009-N-0380; FDA-2013-N-0514; FDA-2013-N-0190; FDA-2010-D-0350; FDA-2016-N-0538; FDA-2013-N-1428] Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration
(FDA)is publishing a list of information collections that have been approved by the Office of Management and Budget
(OMB)under the Paperwork Reduction Act of 1995. FOR FURTHER INFORMATION CONTACT: Ila S. Mizrachi, FDA PRA Staff, Office of Operations, Food and Drug Administration, Three White Flint North, 11601 Landsdown St., North Bethesda, MD 20852, 301-796-7726, *PRAStaff@fda.hhs.gov.* SUPPLEMENTARY INFORMATION: The following is a list of FDA information collections recently approved by OMB under section 3507 of the Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control number and expiration date of OMB approval for each information collection are shown in table 1. Copies of the supporting statements for the information collections are available on the Internet at *http://www.reginfo.gov/public/do/PRAMain.* An Agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. Table 1—List of Information Collections Approved by OMB Title of collection OMB control No. Date approval expires Importer's Entry Notice 0910-0046 12/31/2019 Threshold of Regulation for Substances Used in Food-Contact Articles 0910-0298 12/31/2019 Regulations Restricting the Sale and Distribution of Cigarettes and Smokeless Tobacco to Protect Children and Adolescents 0910-0312 12/31/2019 Postmarket Surveillance of Medical Devices 0910-0449 12/31/2019 Product Jurisdiction: Assignment of Agency Component for Review of Premarket Applications 0910-0523 12/31/2019 Administrative Procedures for Clinical laboratory Improvement Amendments of 1988 Categorization (42 CFR 493.17) 0910-0607 12/31/2019 Requirements under the Comprehensive Smokeless Tobacco Health Education Act of 1986; as amended by the Family Smoking Prevention and Tobacco Control Act 0910-0671 12/31/2019 Guidance for Industry on Tobacco Retailer Training Programs 0910-0745 12/31/2019 Animation in Direct-to-Consumer Advertising 0910-0826 12/31/2019 Guidance for Industry: Electronic Drug Product Reporting for Human Drug Compounding Outsourcing Facilities Under Section 503B of the Federal Food, Drug, and Cosmetic Act 0910-0827 12/31/2019 Dated: May 18, 2017. Anna K. Abram, Deputy Commissioner for Policy, Planning, Legislation, and Analysis. [FR Doc. 2017-10711 Filed 5-24-17; 8:45 am]
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- 42 CFR 493.17
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