Agency Information Collection Activities; Proposed Collection; Comment Request; Registration and Product Listing for Owners and Operators of Domestic Tobacco Product Establishments and Listing of Ingredients in Tobacco Products; Correction, 57568 [2012-22919]

Download as PDF 57568 Federal Register / Vol. 77, No. 181 / Tuesday, September 18, 2012 / Notices agreed to international standards on reporting public health incidents of concern under IHR (2005). Additionally, a majority of States Parties have also agreed to specific work-frames for pathogens such as smallpox under the Biological Weapons Convention. Since May 1999, when the 52nd World Health Assembly (WHA) resolved to postpone the destruction of the Variola virus to allow for essential research (WHA 52.10), WHO has been charged with convening a group of experts to advise on the need for continuing such research, to review proposals for research involving viable Variola virus, to review the progress of such research, and to report to the WHA each year. The need to support the activities described in this project has not changed. In fact, WHO Member States continue to exert pressure for the WHO Secretariat to carry out this work. The WHO Advisory Committee on Variola Virus Research (ACVVR) was established in 1999 to determine what essential research, if any, must be carried out with live Variola virus. The ACVVR monitored the research progress in order to reach global consensus on the timing for the destruction of existing Variola virus stocks. In 2007, the WHA requested the ACVVR undertake a thorough review of the approved research program with a report presented in 2010. The results were presented at the 64th WHA meeting in May of 2011. The ACVVR continues to serve a critically important function for global public health, and to oversee research requested specifically by the U.S. to complete its national strategic goals. This includes the development of new antiviral agents, safer vaccines, and better diagnostics, thus strengthening our national security. Additional Information: The agency program contact is Richard J. Hatchett, MD, who can be contacted by phone at (202) 260–0150 or via email at Richard.Hatchett@hhs.gov. Dated: September 12, 2012. Nicole Lurie, Assistant Secretary for Preparedness and Response. mstockstill on DSK4VPTVN1PROD with NOTICES [FR Doc. 2012–23017 Filed 9–17–12; 8:45 am] BILLING CODE 4150–37–P VerDate Mar<15>2010 18:39 Sep 17, 2012 Jkt 226001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2012–N–0386] Food and Drug Administration, HHS. ACTION: Notice; correction. The Food and Drug Administration (FDA) is correcting a notice that appeared in the Federal Register of May 3, 2012 (77 FR 26281). The document announced an opportunity for public comment on the proposed extension of an existing collection of information by the Agency pertaining to registration and product listing for owners and operators of domestic tobacco product establishments and to listing of ingredients in tobacco products under the Family Smoking Prevention and Tobacco Control Act. The document published with incorrect FDA form numbers. This document corrects those errors. FOR FURTHER INFORMATION CONTACT: Daniel Gittleson, Office of Information Management, Food and Drug Administration, 1350 Piccard Dr., PI50– 400B, Rockville, MD 20850, 301–796– 5156, Daniel.Gittleson@fda.hhs.gov. SUPPLEMENTARY INFORMATION: In FR Doc. 2012–10645 appearing on page 26281 in the Federal Register of Thursday, May 3, 2012, the following corrections are made: 1. On page 26282, in the third column, in the first full paragraph, the fifth sentence ‘‘FDA also developed paper forms (Form FDA 3742— Registration and Listing for Owners and Operators of Domestic Tobacco Product Establishments and Form FDA 3743— Listing of Ingredients in Tobacco Products) as an alternative submission tool.’’ is corrected to read ‘‘FDA also developed paper forms (Form FDA 3741—Registration and Listing for Owners and Operators of Domestic Tobacco Product Establishments and Form FDA 3742—Listing of Ingredients in Tobacco Products) as an alternative submission tool.’’ 2. On page 26283, in the table, ‘‘Form FDA 3742’’ is corrected to read ‘‘Form FDA 3741’’ and ‘‘Form FDA 3743’’ is corrected to read ‘‘Form FDA 3742’’. SUMMARY: PO 00000 Frm 00013 Fmt 4703 Sfmt 4703 [FR Doc. 2012–22919 Filed 9–17–12; 8:45 am] BILLING CODE 4160–01–P Agency Information Collection Activities; Proposed Collection; Comment Request; Registration and Product Listing for Owners and Operators of Domestic Tobacco Product Establishments and Listing of Ingredients in Tobacco Products; Correction AGENCY: Dated: September 12, 2012. Leslie Kux, Assistant Commissioner for Policy. DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2012–N–0386] Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Registration and Product Listing for Owners and Operators of Domestic Tobacco Product Establishments and Listing of Ingredients in Tobacco Products; Correction AGENCY: Food and Drug Administration, HHS. ACTION: Notice; correction. The Food and Drug Administration (FDA) is correcting a notice that appeared in the Federal Register of August 3, 2012 (77 FR 46441). The document announced that a proposed collection of information had been submitted to the Office of Management and Budget for review and clearance under the Paperwork Reduction Act of 1995. The document published with incorrect FDA form numbers. This document corrects those errors. FOR FURTHER INFORMATION CONTACT: Daniel Gittleson, Office of Information Management, Food and Drug Administration, 1350 Piccard Dr., PI50– 400B, Rockville, MD 20850, 301–796– 5156, Daniel.Gittleson@fda.hhs.gov. SUPPLEMENTARY INFORMATION: In FR Doc. 2012–18975 appearing on page 46441 in the Federal Register of Friday, August 3, 2012, the following corrections are made: 1. On page 46442, in the third column, in the first full paragraph, the fifth sentence ‘‘FDA also developed paper forms (Form FDA 3742— Registration and Listing for Owners and Operators of Domestic Tobacco Product Establishments and Form FDA 3743— Listing of Ingredients in Tobacco Products) as an alternative submission tool.’’ is corrected to read ‘‘FDA also developed paper forms (Form FDA 3741—Registration and Listing for Owners and Operators of Domestic Tobacco Product Establishments and Form FDA 3742—Listing of Ingredients in Tobacco Products) as an alternative submission tool.’’ SUMMARY: E:\FR\FM\18SEN1.SGM 18SEN1

Agencies

[Federal Register Volume 77, Number 181 (Tuesday, September 18, 2012)]
[Notices]
[Page 57568]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-22919]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2012-N-0386]


Agency Information Collection Activities; Proposed Collection; 
Comment Request; Registration and Product Listing for Owners and 
Operators of Domestic Tobacco Product Establishments and Listing of 
Ingredients in Tobacco Products; Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice; correction.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) is correcting a notice 
that appeared in the Federal Register of May 3, 2012 (77 FR 26281). The 
document announced an opportunity for public comment on the proposed 
extension of an existing collection of information by the Agency 
pertaining to registration and product listing for owners and operators 
of domestic tobacco product establishments and to listing of 
ingredients in tobacco products under the Family Smoking Prevention and 
Tobacco Control Act. The document published with incorrect FDA form 
numbers. This document corrects those errors.

FOR FURTHER INFORMATION CONTACT: Daniel Gittleson, Office of 
Information Management, Food and Drug Administration, 1350 Piccard Dr., 
PI50-400B, Rockville, MD 20850, 301-796-5156, 
Daniel.Gittleson@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: In FR Doc. 2012-10645 appearing on page 
26281 in the Federal Register of Thursday, May 3, 2012, the following 
corrections are made:
    1. On page 26282, in the third column, in the first full paragraph, 
the fifth sentence ``FDA also developed paper forms (Form FDA 3742--
Registration and Listing for Owners and Operators of Domestic Tobacco 
Product Establishments and Form FDA 3743--Listing of Ingredients in 
Tobacco Products) as an alternative submission tool.'' is corrected to 
read ``FDA also developed paper forms (Form FDA 3741--Registration and 
Listing for Owners and Operators of Domestic Tobacco Product 
Establishments and Form FDA 3742--Listing of Ingredients in Tobacco 
Products) as an alternative submission tool.''
    2. On page 26283, in the table, ``Form FDA 3742'' is corrected to 
read ``Form FDA 3741'' and ``Form FDA 3743'' is corrected to read 
``Form FDA 3742''.

    Dated: September 12, 2012.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2012-22919 Filed 9-17-12; 8:45 am]
BILLING CODE 4160-01-P
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.