Submission for OMB Review; Comment Request, 63714-63715 [E8-25419]

Download as PDF 63714 Federal Register / Vol. 73, No. 208 / Monday, October 27, 2008 / Notices Hotel Palomar Arlington, 1121 North 19th Street, Arlington, VA 22209. Phone 703–351–9170. FOR FURTHER INFORMATION CONTACT: Ms. Diane M. Gianelli, Director of Communications, The President’s Council on Bioethics, 1425 New York Avenue, NW., Suite C100, Washington, DC 20005. Telephone: 202/296–4669. Email: info@bioethics.gov. Web site: https://www.bioethics.gov. SUPPLEMENTARY INFORMATION: The meeting agenda will be posted at https://www.bioethics.gov. The Council encourages public input, either in person or in writing. At this meeting, interested members of the public may address the Council, beginning at 11:45 a.m. on Friday, November 21. Comments are limited to no more than five minutes per speaker or organization. As a courtesy, please inform Ms. Diane M. Gianelli, Director of Communications, in advance of your intention to make a public statement, and give your name and affiliation. To submit a written statement, mail or email it to Ms. Gianelli at one of her contact addresses given above. ADDRESSES: Dated: October 17, 2008. F. Daniel Davis, Executive Director, The President’s Council on Bioethics. [FR Doc. E8–25564 Filed 10–24–08; 8:45 am] BILLING CODE 4154–06–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Office of the Secretary Notice of Meeting: Secretary’s Advisory Committee on Genetics, Health, and Society Pursuant to Public Law 92–463, notice is hereby given of the 17th meeting of the Secretary’s Advisory Committee on Genetics, Health, and Society (SACGHS), U.S. Public Health Service. The meeting will be held from 8 a.m. to approximately 5:30 p.m. on Monday, December 1, 2008, and 8 a.m. to approximately 3 p.m. on Tuesday, December 2, 2008, at the Hubert H. Humphrey Building, 200 Independence Avenue, SW., Washington, DC 20201. The meeting will be open to the public with attendance limited to space available. The meeting also will be Web cast. For most of the first day of the meeting, SACGHS will review a preliminary draft report that addresses questions about whether gene patents and certain licensing practices are affecting patient access to genetic tests. SACGHS will discuss the draft report and determine whether it is ready to be released for public comment. Later in the day, the Committee will hear presentations about diagnostic laboratory standards and technology platforms and the role they are playing in innovation of genetic technologies. On day two, the Committee will continue to discuss priority issues and future study topics and come to a final decision about its strategic study plan. As always, the Committee welcomes hearing from anyone wishing to provide public comment on any issue related to genetics, health and society. Individuals who would like to provide public comment should notify the SACGHS Executive Secretary, Ms. Sarah Carr, by telephone at 301–496–9838 or e-mail at carrs@od.nih.gov. The SACGHS office is located at 6705 Rockledge Drive, Suite 750, Bethesda, MD 20892. Anyone planning to attend the meeting, who is in need of special assistance, such as sign language interpretation or other reasonable accommodations, is also asked to contact the Executive Secretary. Under authority of 42 U.S.C. 217a, Section 222 of the Public Health Service Act, as amended, the Department of Health and Human Services established SACGHS to serve as a public forum for deliberations on the broad range of human health and societal issues raised by the development and use of genetic and genomic technologies and, as warranted, to provide advice on these issues. The draft meeting agenda and other information about SACGHS, including information about access to the Web cast, will be available at the following Web site: https:// www4.od.nih.gov/oba/sacghs.htm. Dated: October 20, 2008. Jennifer Spaeth, Director, NIH Office of Federal Advisory Committee Policy. [FR Doc. E8–25486 Filed 10–24–08; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: Grants to States for Access and Visitation. OMB No.: 0970–0204. Description: On an annual basis, States must provide OCSE with data on programs that the Grants to States for Access and Visitation Program has funded. These program reporting requirements include, but are not limited to, the collection of data on the number of parents served, types of services delivered, program outcomes, client socio economic data, referrals sources, and other relevant data. Respondents: State Child Access and Visitation Programs and State and/or local service providers. ANNUAL BURDEN ESTIMATES mstockstill on PROD1PC66 with NOTICES State Child Access Program Survey ............................................... Estimated Total Annual Burden Hours: 4,710. Additional Information: Copies of the proposed collection may be obtained by writing to the Administration for Children and Families, Office of Administration, Office of Information Services, 370 L’Enfant Promenade, SW., Washington, DC 20447, Attn: ACF VerDate Aug<31>2005 17:13 Oct 24, 2008 Jkt 217001 Number of responses per respondent Number of respondents Instrument 314 Reports Clearance Officer. All requests should be identified by the title of the information collection. E-mail 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. PO 00000 Frm 00042 Fmt 4703 Sfmt 4703 Average burden hours per response 1 15 Total burden hours 4,710 Therefore, a comment is best assured of having its full effect if OMB receives it within 30 days of publication. Written comments and recommendations for the proposed information collection should be sent directly to the following: Office of Management and Budget, Paperwork Reduction Project, Attn: Desk Officer for E:\FR\FM\27OCN1.SGM 27OCN1 Federal Register / Vol. 73, No. 208 / Monday, October 27, 2008 / Notices ACE, E-mail address: Karen_T._Matsuoka@omb.eop.gov. Dated: October 20, 2008. Janean Chambers, Reports Clearance Officer. [FR Doc. E8–25419 Filed 10–24–08; 8:45 am] BILLING CODE 4184–01–M DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2008–N–0038] Intrapartum Electronic Fetal Monitoring With Computer Assisted Diagnosis Workshop—Exploring Methods of Evaluation AGENCY: Food and Drug Administration, HHS mstockstill on PROD1PC66 with NOTICES ACTION: Notice of public workshop. The Food and Drug Administration (FDA) is announcing a public workshop entitled ‘‘Intrapartum Electronic Fetal Monitoring (EFM) With Computer Assisted Diagnosis (CAD)—Exploring Methods of Evaluation.’’ The objectives of this workshop are to gather ideas on how to identify and differentiate categories of EFM/CAD devices and the corresponding levels of evidence needed to validate these devices. Workshop participants will also discuss how currently available databases might be used to verify/validate intrapartum EFM/CAD algorithms. Date and Time: The workshop will be held on November 10, 2008, from 8 a.m. to 5 p.m. Registrations will be accepted through October 31, 2008. Participants are encouraged to arrive early to ensure time for parking, security screening, and registration before the meeting. Security screening will begin at 7 a.m. and registration will begin at 7:30 a.m. See Registration Information section of this document for registration details. Location: The workshop will be held at the Food & Drug Administration White Oak Campus, conference room G– 2047, 10903 New Hampshire Ave., Silver Spring, MD 20993. FDA will make every effort to accommodate persons with physical disabilities or special needs. If you require special accommodations due to a disability, please notify one of the contacts listed in this document (see Contact) at least 7 days in advance of the workshop. Contact: Sharon Andrews, Center for Devices and Radiological Health (HFZ– 470), Food and Drug Administration, 9200 Corporate Blvd., Rockville, MD 20850, 240–276–4148, FAX: 240–276– 4156, sharon.andrews@fda.hhs.gov; or VerDate Aug<31>2005 17:13 Oct 24, 2008 Jkt 217001 Elaine Blyskun, Center for Devices and Radiological Health (HFZ–470), Food and Drug Administration, 9200 Corporate Blvd., Rockville, MD 20850, 240–276–4100, FAX: 240–276–4156, elaine.blyskun@fda.hhs.gov. Registration Information: Registration may be completed online at the following Web site: https:// www.blsmeetings.net/1368-2. There is no registration fee for this workshop; however, all participants must submit a registration form. Space is limited, so please register as soon as possible to reserve a space. Registrations will be accepted through (see DATES). Persons without Internet access may contact Syreeta Tate-Jones at 301–577–0244, ext. 49 by October 31, 2008, to register. Agenda: The workshop will begin with a morning session to provide a clinical and regulatory overview of intrapartum fetal monitors. Presentation topics will address fetal monitoring in general, the relationship between technology and clinical decisionmaking, the current state of EFM/CAD development, and evaluation/validation methods that may be applied to new EFM/CAD systems. In the afternoon, attendees will break into two discussion groups: (1) EFM/CAD technological development and validation and (2) the practicality of using existing databases to test new EFM/CAD algorithms. The workshop will conclude with an overview of the break-out discussions and identification of research gaps and opportunities in the field. Dated: October 20, 2008. Jeffrey Shuren, Associate Commissioner for Policy and Planning. [FR Doc. E8–25586 Filed 10–24–08; 8:45 am] BILLING CODE 4160–01–S 63715 Status: The meeting will be open to the public. Purpose: The Advisory Committee provides advice and recommendations on a broad range of issues dealing with programs and activities authorized under section 747 of the Public Health Service Act as amended by The Health Professions Education Partnership Act of 1998, Public Law 105– 392. At this meeting the Advisory Committee will work on its eighth report about the redesign of the delivery of primary health care and its implications for the training of primary care practitioners. Reports are submitted to Congress and to the Secretary of the Department of Health and Human Services. Agenda: The meeting on Monday, November 17, will begin with opening comments from the Chair of the Advisory Committee and introductory remarks from senior management of the Health Resources and Services Administration. The Advisory Committee will elect a new chair and two vice-chairs prior to the main agenda. In the plenary session, the Advisory Committee will discuss key elements they wish to include in the eighth report, develop an outline for the report, and draft report recommendations. The work will be done in plenary session and in small groups. On Tuesday, November 18, the Advisory Committee will continue its work on the eighth report and determine next steps in the report preparation process. The members will plan an agenda for the next Advisory Committee meeting. An opportunity will be provided for public comment. For Further Information Contact: Anyone interested in obtaining a roster of members or other relevant information should write or contact Jerilyn K. Glass, M.D., PhD, Division of Medicine and Dentistry, Bureau of Health Professions, Health Resources and Services Administration, Room 9A–27, Parklawn Building, 5600 Fishers Lane, Rockville, Maryland 20857, Telephone (301) 443–6822. The Web address for information on the Advisory Committee is https://bhpr.hrsa.gov/ medicine-dentistry/actpcmd. DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration Dated: October 21, 2008. Alexandra Huttinger, Director, Division of Policy Review and Coordination. [FR Doc. E8–25569 Filed 10–24–08; 8:45 am] BILLING CODE 4165–15–P Advisory Committee on Training in Primary Care Medicine and Dentistry; Notice of Meeting In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Public Law 92–463), notice is hereby given of the following meeting: Name: Advisory Committee on Training in Primary Care Medicine and Dentistry (ACTPCMD). Date and Time: November 17, 2008, 8:30 a.m.–4:30 p.m. November 18, 2008, 8 a.m.– 2 p.m. Place: The Legacy Hotel and Meeting Centre, 1775 Rockville Pike, Rockville, Maryland 20852. PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration National Advisory Council on Nurse Education and Practice; Notice of Meeting In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Public Law 92–463), notice is hereby given of the following meeting: Name: National Advisory Council on Nurse Education and Practice (NACNEP). E:\FR\FM\27OCN1.SGM 27OCN1

Agencies

[Federal Register Volume 73, Number 208 (Monday, October 27, 2008)]
[Notices]
[Pages 63714-63715]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-25419]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for OMB Review; Comment Request

    Title: Grants to States for Access and Visitation.
    OMB No.: 0970-0204.
    Description: On an annual basis, States must provide OCSE with data 
on programs that the Grants to States for Access and Visitation Program 
has funded. These program reporting requirements include, but are not 
limited to, the collection of data on the number of parents served, 
types of services delivered, program outcomes, client socio economic 
data, referrals sources, and other relevant data.
    Respondents: State Child Access and Visitation Programs and State 
and/or local service providers.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                Number of      Average burden
               Instrument                     Number of       responses per       hours per       Total burden
                                             respondents       respondent         response            hours
----------------------------------------------------------------------------------------------------------------
State Child Access Program Survey.......               314                 1                15             4,710
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 4,710.
    Additional Information: Copies of the proposed collection may be 
obtained by writing to the Administration for Children and Families, 
Office of Administration, Office of Information Services, 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. E-mail 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 recommendations for the proposed 
information collection should be sent directly to the following: Office 
of Management and Budget, Paperwork Reduction Project, Attn: Desk 
Officer for

[[Page 63715]]

ACE, E-mail address: Karen_T._Matsuoka@omb.eop.gov.

    Dated: October 20, 2008.
Janean Chambers,
Reports Clearance Officer.
 [FR Doc. E8-25419 Filed 10-24-08; 8:45 am]
BILLING CODE 4184-01-M
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