Board of Scientific Counselors, National Center for Health Statistics (BSC, NCHS), 82030 [2010-32747]

Download as PDF 82030 Federal Register / Vol. 75, No. 249 / Wednesday, December 29, 2010 / Notices on the Internet at https://www.gsa.gov/ ftr. This process, implemented in FTR Amendment 2010–07 (75 FR 72965, Nov. 29, 2010), ensures more timely updates in mileage reimbursement rates by GSA for Federal employees on official travel. Notices published periodically in the Federal Register, such as this one, and the changes posted on the GSA Web site, now constitute the only notification of revisions to privately owned vehicle reimbursement rates for Federal agencies. single-spaced typedpages in length and must be received by January 21, 2011. The agenda is subject to change as priorities dictate. Contact Person for More Information: Virginia S. Cain, PhD, Director of Extramural Research, NCHS/CDC, 3311 Toledo Road, Room 7211, Hyattsville, Maryland 20782, telephone (301) 458–4500, fax (301) 458– 4020. BILLING CODE 6820–14–P The Director, Management Analysis and Services Office, has been delegated the authority to sign Federal Register notices pertaining to announcements of meetings and othercommittee management activities, for both the Centers for Disease Control and Prevention, and the Agency for Toxic Substances and Disease Registry. DEPARTMENT OF HEALTH AND HUMAN SERVICES Dated: December 21, 2010. Elaine L. Baker, Management Analysis and Services Office, Centers for Disease Control and Prevention. Dated: December 21, 2010. Janet Dobbs, Acting Deputy Associate Administrator. [FR Doc. 2010–32773 Filed 12–28–10; 8:45 am] [FR Doc. 2010–32747 Filed 12–28–10; 8:45 am] Centers for Disease Control and Prevention BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES srobinson on DSKHWCL6B1PROD with NOTICES In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Pub. L. 92–463), the Centers for Disease Control and Prevention (CDC), NCHS announces the following meeting of the aforementioned committee: Times and Dates: 11 a.m.–5:30 p.m., January 27, 2011. 8:30 a.m.–2 p.m., January 28, 2011. Place: NCHS Headquarters, 3311 Toledo Road, Hyattsville, Maryland 20782. Status: This meeting is open to the public; however, visitors must be processed in accordance with established federal policies and procedures. Pre-approval is required for foreign nationals or non-US citizens. Please contact Althelia Harris, 301–458–4261, adw1@cdc.gov or Virginia Cain, vcain@cdc.gov at least 10 days in advance for requirements. All visitors are required to present a valid form of picture identification issued by a State, Federal or international government. The meeting room accommodates approximately 100 people. Purpose: This committee provides advice and makes recommendations to the Secretary, HHS; the Director, CDC; and the Director, NCHS, regarding the scientific and technical program goals and objectives, strategies, and priorities of NCHS. Matters to be Discussed: The agenda will include welcome remarks by the Director, NCHS; an update on the Health Indicators Warehouse; an update on program reviews; and an open session for comments from the public. Requests to make oral presentations should be submitted in writing to the contact person listed below. All requests must contain the name, address, telephone number, and organizational affiliation of the presenter. Written comments should not exceed five 02:10 Dec 29, 2010 Jkt 223001 Submit either electronic or written comments on the collection of information by February 28, 2011. DATES: Submit electronic comments on the collection of information to https:// www.regulations.gov. Submit written comments on the collection of information to the Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. All comments should be identified with the docket number found in brackets in the heading of this document. ADDRESSES: FOR FURTHER INFORMATION CONTACT: Denver Presley, Jr., Office of Information Management, Food and Drug Administration, 1350 Piccard Dr., PI50– 400B, Rockville, MD 20850, 301–796– 3793. Under the PRA (44 U.S.C. 3501–3520), Federal Agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. ‘‘Collection of information’’ is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and includes Agency requests or requirements that members of the public submit reports, keep records, or provide information to a third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires Federal Agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information before submitting the collection to OMB for approval. To comply with this requirement, FDA is publishing notice of the proposed collection of information set forth in this document. With respect to the following collection of information, FDA invites comments on these topics: (1) Whether the proposed collection of information is necessary for the proper performance of FDA’s functions, including whether the information will have practical utility; (2) the accuracy of FDA’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques, when appropriate, and other forms of information technology. SUPPLEMENTARY INFORMATION: Board of Scientific Counselors, National Center for Health Statistics (BSC, NCHS) VerDate Mar<15>2010 online sales of food products, and consumer and professional education. Food and Drug Administration [Docket No. FDA–2010–N–0640] Agency Information Collection Activities; Proposed Collection; Comment Request; Data to Support Food and Nutrition Product Communications, as Used by the Food and Drug Administration AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (the PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information and to allow 60 days for public comment in response to the notice. This notice solicits comments on a generic clearance to collect information to support communications about nutrition and food products regulated by FDA. This data collection will gauge, informally, public opinion on a variety of subjects related to consumer, patient, or health care professional perceptions and use of nutrition and food products and related materials, including but not limited to, food advertising, food and nutrition labeling, emerging risk communications, SUMMARY: PO 00000 Frm 00066 Fmt 4703 Sfmt 4703 E:\FR\FM\29DEN1.SGM 29DEN1

Agencies

[Federal Register Volume 75, Number 249 (Wednesday, December 29, 2010)]
[Notices]
[Page 82030]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-32747]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention


Board of Scientific Counselors, National Center for Health 
Statistics (BSC, NCHS)

    In accordance with section 10(a)(2) of the Federal Advisory 
Committee Act (Pub. L. 92-463), the Centers for Disease Control and 
Prevention (CDC), NCHS announces the following meeting of the 
aforementioned committee:

    Times and Dates: 11 a.m.-5:30 p.m., January 27, 2011. 8:30 a.m.-
2 p.m., January 28, 2011.
    Place: NCHS Headquarters, 3311 Toledo Road, Hyattsville, 
Maryland 20782.
    Status: This meeting is open to the public; however, visitors 
must be processed in accordance with established federal policies 
and procedures. Pre-approval is required for foreign nationals or 
non-US citizens. Please contact Althelia Harris, 301-458-4261, 
adw1@cdc.gov or Virginia Cain, vcain@cdc.gov at least 10 days in 
advance for requirements. All visitors are required to present a 
valid form of picture identification issued by a State, Federal or 
international government. The meeting room accommodates 
approximately 100 people.
    Purpose: This committee provides advice and makes 
recommendations to the Secretary, HHS; the Director, CDC; and the 
Director, NCHS, regarding the scientific and technical program goals 
and objectives, strategies, and priorities of NCHS.
    Matters to be Discussed: The agenda will include welcome remarks 
by the Director, NCHS; an update on the Health Indicators Warehouse; 
an update on program reviews; and an open session for comments from 
the public.
    Requests to make oral presentations should be submitted in 
writing to the contact person listed below. All requests must 
contain the name, address, telephone number, and organizational 
affiliation of the presenter. Written comments should not exceed 
five single-spaced typedpages in length and must be received by 
January 21, 2011.
    The agenda is subject to change as priorities dictate.
    Contact Person for More Information: Virginia S. Cain, PhD, 
Director of Extramural Research, NCHS/CDC, 3311 Toledo Road, Room 
7211, Hyattsville, Maryland 20782, telephone (301) 458-4500, fax 
(301) 458-4020.

    The Director, Management Analysis and Services Office, has been 
delegated the authority to sign Federal Register notices pertaining to 
announcements of meetings and othercommittee management activities, for 
both the Centers for Disease Control and Prevention, and the Agency for 
Toxic Substances and Disease Registry.

    Dated: December 21, 2010.
Elaine L. Baker,
Management Analysis and Services Office, Centers for Disease Control 
and Prevention.
[FR Doc. 2010-32747 Filed 12-28-10; 8:45 am]
BILLING CODE 4163-18-P
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