Food Advisory Committee; Notice of Meeting; Amendment of Notice, 67438-67439 [2014-26823]

Download as PDF 67438 Federal Register / Vol. 79, No. 219 / Thursday, November 13, 2014 / Notices to read ‘‘Current Status of Expected Results and Benefits.’’ The content requested in this section is similar to the previous OPR without the added burden of having the reporting organizations provide the analysis that distinguish between ‘‘results and benefits’’. Every section of the document will be rewritten to reflect this change. OWP: ANA proposes to reformat the OWP (content is same) by swapping the Objective field with Problem Statement. In other words, this section will require respondents to begin with a concise statement about the problem the project is designed to address and will be followed by more details about the objectives of the project. The two fields ‘‘Results Expected and Benefits Expected’’ will be combined into one field to read ‘‘Results and benefits Expected’’. This will reduce redundancy and help reduce the burden on Grantees. Respondents: Tribal Government, Native non-profit organizations, Tribal Colleges & Universities. ANNUAL BURDEN ESTIMATES Number of respondents Instrument OWP ................................................................................................................ OPR ................................................................................................................. Estimated Total Annual Burden Hours: 2,050. Additional Information: Copies of the proposed collection may be obtained by writing to the Administration for Children and Families, Office of Planning, Research and Evaluation, 370 L’Enfant Promenade SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. All requests should be identified by the title of the information collection. Email address: infocollection@acf.hhs.gov. OMB Comment: OMB is required to make a decision concerning the collection of information between 30 and 60 days after publication of this document in the Federal Register. Therefore, a comment is best assured of having its full effect if OMB receives it within 30 days of publication. Written comments and recommendation for the proposed information collection should be sent directly to the following: Office of Management and Budget, Paperwork Reduction Project, Fax: 202–395–7285, Email: OIRA_SUBMISSION@ OMB.EOP.GOV, Attn: Desk Officer for the Administration for Children and families. Robert Sargis, Reports Clearance Officer. [FR Doc. 2014–26785 Filed 11–12–14; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES tkelley on DSK3SPTVN1PROD with NOTICES Food and Drug Administration [Docket No. FDA–2014–N–0001] Science Board to the Food and Drug Administration Advisory Committee Meeting; Amendment of Notice AGENCY: Food and Drug Administration, ACTION: 17:16 Nov 12, 2014 Jkt 235001 500 275 Notice. The Food and Drug Administration (FDA) is announcing an amendment to the notice of meeting of the Science Board to the Food and Drug Administration. This meeting was announced in the Federal Register of October 8, 2014. The amendment is being made to reflect changes in URL for the Webcast. There are no other changes. SUMMARY: Average burden hours per response 1 2 Total burden hours 3 1 1,500 550 Dated: November 5, 2014. Jill Hartzler Warner, Associate Commissioner for Special Medical Programs. [FR Doc. 2014–26821 Filed 11–12–14; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2014–N–1732] FOR FURTHER INFORMATION CONTACT: Martha Monser, Office of the Chief Scientist, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 1, Rm. 3309, Silver Spring, MD 20993, 301–796–4627, or FDA Advisory Committee Information Line, 1–800–741–8138 (301–443–0572 in the Washington, DC area). Please call the Information Line for up-to-date information on this meeting. In the Federal Register of October 8, 2014 (79 FR 60856), FDA announced that a meeting of the Science Board to the Food and Drug Administration would be held on November 19 and 20, 2014. On page 60857, in the first column, the URL information is changed to read as follows: The link for the Webcast on November 19, 2014, is available at: https://collaboration.fda.gov/ scienceboard111914/. The link for the Webcast on November 20, 2014, is available at: https:// collaboration.fda.gov/scienceboard 112014. This notice is issued under the Federal Advisory Committee Act (5 U.S.C. app. 2) and 21 CFR part 14, relating to the advisory committees. SUPPLEMENTARY INFORMATION: HHS. VerDate Sep<11>2014 Number of responses per respondent PO 00000 Frm 00027 Fmt 4703 Sfmt 4703 Food Advisory Committee; Notice of Meeting; Amendment of Notice AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is announcing an amendment to the notice of the meeting of the Food Advisory Committee. This meeting was announced in the Federal Register of August 19, 2014. The amendment is being made to add an ADDRESSES section and to reflect a change in the Agenda. There are no other changes. FOR FURTHER INFORMATION CONTACT: Karen Strambler, Center for Food Safety and Applied Nutrition, Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740, 240– 402–2589, FAX: 301–436–2637, email: FoodAdvisoryCommittee@fda.hhs.gov, or FDA Advisory Committee Information Line, 1–800–741–8138 (301–443–0572 in the Washington, DC area) and follow the prompts to the desired Center or product area. Please call the Information Line for up-to-date information on this meeting. SUPPLEMENTARY INFORMATION: In the Federal Register of August 19, 2014 (79 FR 49091), FDA announced that a meeting of the Food Advisory SUMMARY: E:\FR\FM\13NON1.SGM 13NON1 Federal Register / Vol. 79, No. 219 / Thursday, November 13, 2014 / Notices Committee would be held on December 16–17, 2014. The ADDRESSES portion of the document is to read as follows: ADDRESSES: FDA is opening a docket for public comment on this meeting. The docket will open for public comment on November 13, 2014. The docket will close on January 15, 2014. Interested persons may submit either electronic comments regarding this meeting to http://www.regulations.gov or written comments to the Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. It is only necessary to send one set of comments. Identify comments with the docket number found in brackets in the heading of this document. Received comments may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday, and will be posted to the docket at http:// www.regulations.gov. All comments received will be posted without changes, including any personal information provided. Comments received on or before December 1, 2014, will be provided to the committee before the meeting. On page 49091, in the second column, the Agenda portion of the document is changed to read as follows: Agenda: The committee will discuss how risk assessments should account for the susceptibility to the effects of a particular chemical exposure because of factors such as genetics, age, sex, and health status and the circumstances under which FDA would decide to conduct a separate risk assessment for these groups. This notice is issued under the Federal Advisory Committee Act (5 U.S.C. app. 2) and 21 CFR part 14, relating to the advisory committees. Dated: November 7, 2014. Jill Hartzler Warner, Associate Commissioner for Special Medical Programs. [FR Doc. 2014–26823 Filed 11–12–14; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES tkelley on DSK3SPTVN1PROD with NOTICES Health Resources and Services Administration Agency Information Collection Activities: Proposed Collection: Public Comment Request Health Resources and Services Administration, HHS. AGENCY: VerDate Sep<11>2014 17:16 Nov 12, 2014 Jkt 235001 ACTION: Notice. In compliance with the requirement for opportunity for public comment on proposed data collection projects (Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995), the Health Resources and Services Administration (HRSA) announces plans to submit an Information Collection Request (ICR), described below, to the Office of Management and Budget (OMB). Prior to submitting the ICR to OMB, HRSA seeks comments from the public regarding the burden estimate, below, or any other aspect of the ICR. DATES: Comments on this Information Collection Request must be received no later than January 12, 2015. ADDRESSES: Submit your comments to paperwork@hrsa.gov or mail the HRSA Information Collection Clearance Officer, Room 10C–03, Parklawn Building, 5600 Fishers Lane, Rockville, MD 20857. FOR FURTHER INFORMATION CONTACT: To request more information on the proposed project or to obtain a copy of the data collection plans and draft instruments, email paperwork@hrsa.gov or call the HRSA Information Collection Clearance Officer at (301) 443–1984. SUPPLEMENTARY INFORMATION: When submitting comments or requesting information, please include the information request collection title for reference. Information Collection Request Title: Evaluation and Initial Assessment of the HRSA Teaching Health Centers Graduate Medical Education Program. OMB No.: 0906–xxxx—New. Abstract: Section 5508 of the Affordable Care Act of 2010 amended section 340H of the Public Health Service Act to establish the Teaching Health Center Graduate Medical Education (THCGME) program to provide funding support for new and the expansion of existing primary care residency training programs in community-based settings. The primary goals of this program is to increase the production of primary care providers who are better prepared to practice in community settings, particularly with underserved populations, and improve the geographic distribution of primary care providers. Statute requires the Secretary to determine an appropriate THCGME program payment for indirect medical expenses (IME) as well as to update, as deemed appropriate, the per resident SUMMARY: PO 00000 Frm 00028 Fmt 4703 Sfmt 4703 67439 amount used to determine the Program’s payment for direct medical expenses (DME). To inform these determinations and to increase understanding of this model of residency training, the George Washington University (GW) is conducting an evaluation of the costs associated with training residents in the Teaching Health Center (THC) model. GW has developed a standardized costing instrument to gather data from all THCGME programs. The information gathered in the standardized costing instrument includes, but is not limited to, resident and faculty full-time equivalents, salaries and benefits, residency administration costs, educational costs, residency clinical operations and administrative costs, and patient visits and clinical revenue generated by medical residents. Need and Proposed Use of the Information: HRSA is collecting costing information related to both DME and IME in an effort to establish a THC’s total cost of running a residency program, to assist the Secretary in determining an appropriate update to the per resident amount used to calculate the payment for DME and an appropriate IME payment. The described data collection activities will serve to inform these statutory requirements for the Secretary in a uniform and consistent manner. Likely Respondents: THCGME grantees. Burden Statement: Burden in this context means the time expended by persons to generate, maintain, retain, disclose or provide the information requested. This includes the time needed to review instructions; to develop, acquire, install and utilize technology and systems for the purpose of collecting, validating and verifying information, processing and maintaining information, and disclosing and providing information; to train personnel and to be able to respond to a collection of information; to search data sources; to complete and review the collection of information; and to transmit or otherwise disclose the information. The total annual burden hours estimated for this Information Collection Request are summarized in the table below. The annual estimate of burden is as follows: E:\FR\FM\13NON1.SGM 13NON1

Agencies

[Federal Register Volume 79, Number 219 (Thursday, November 13, 2014)]
[Notices]
[Pages 67438-67439]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-26823]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2014-N-1732]


Food Advisory Committee; Notice of Meeting; Amendment of Notice

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is announcing an 
amendment to the notice of the meeting of the Food Advisory Committee. 
This meeting was announced in the Federal Register of August 19, 2014. 
The amendment is being made to add an ADDRESSES section and to reflect 
a change in the Agenda. There are no other changes.

FOR FURTHER INFORMATION CONTACT: Karen Strambler, Center for Food 
Safety and Applied Nutrition, Food and Drug Administration, 5100 Paint 
Branch Pkwy., College Park, MD 20740, 240-402-2589, FAX: 301-436-2637, 
email: FoodAdvisoryCommittee@fda.hhs.gov, or FDA Advisory Committee 
Information Line, 1-800-741-8138 (301-443-0572 in the Washington, DC 
area) and follow the prompts to the desired Center or product area. 
Please call the Information Line for up-to-date information on this 
meeting.

SUPPLEMENTARY INFORMATION: In the Federal Register of August 19, 2014 
(79 FR 49091), FDA announced that a meeting of the Food Advisory

[[Page 67439]]

Committee would be held on December 16-17, 2014. The ADDRESSES portion 
of the document is to read as follows:

ADDRESSES: FDA is opening a docket for public comment on this meeting. 
The docket will open for public comment on November 13, 2014. The 
docket will close on January 15, 2014. Interested persons may submit 
either electronic comments regarding this meeting to http://www.regulations.gov or written comments to the Division of Dockets 
Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, 
Rm. 1061, Rockville, MD 20852. It is only necessary to send one set of 
comments. Identify comments with the docket number found in brackets in 
the heading of this document. Received comments may be seen in the 
Division of Dockets Management between 9 a.m. and 4 p.m., Monday 
through Friday, and will be posted to the docket at http://www.regulations.gov. All comments received will be posted without 
changes, including any personal information provided. Comments received 
on or before December 1, 2014, will be provided to the committee before 
the meeting.
    On page 49091, in the second column, the Agenda portion of the 
document is changed to read as follows:
    Agenda: The committee will discuss how risk assessments should 
account for the susceptibility to the effects of a particular chemical 
exposure because of factors such as genetics, age, sex, and health 
status and the circumstances under which FDA would decide to conduct a 
separate risk assessment for these groups.
    This notice is issued under the Federal Advisory Committee Act (5 
U.S.C. app. 2) and 21 CFR part 14, relating to the advisory committees.

    Dated: November 7, 2014.
Jill Hartzler Warner,
Associate Commissioner for Special Medical Programs.
[FR Doc. 2014-26823 Filed 11-12-14; 8:45 am]
BILLING CODE 4164-01-P