Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC); Notice of Meeting, 16218-16219 [E9-8136]

Download as PDF 16218 Federal Register / Vol. 74, No. 67 / Thursday, April 9, 2009 / Notices and Budget for review under the Paperwork Reduction Act of 1995: Proposed Project: Uncompensated Services Assurance Report (OMB No. 0915–0077)—[Extension] Under the Hill-Burton Act, the government provides grants and loans for construction or renovation of health care facilities. As a condition of receiving this construction assistance, facilities are required to provide services to persons unable to pay. A condition of receiving this assistance requires facilities to provide assurances periodically that the required level of Responses per respondent Number of respondents Instrument uncompensated care is being provided, and that certain notification and record keeping procedures are being followed. These requirements are referred to as the uncompensated services assurance. The annual estimate of burden is as follows: Total responses Hours per response Total burden hours Disclosure Burden (42 CFR) Published Notices (124.504(c)) ........................................... Individual Notices (124.504(c)) ............................................ Determinations of Eligibility (124.507) ................................. 86 86 86 1 1 99 86 86 8,514 0.75 43.6 0.75 64.5 3,749.6 6,385.50 Subtotal disclosure burden ........................................... ........................ ........................ ........................ ........................ 10,199.60 10 1 10 11.0 110 4 0 2 1 ........................ 1 4 ........................ 2 6.0 ........................ 6.0 24 ........................ 12 37 14 0 1 1 1 37 14 0 0.5 0.5 0.5 18.5 7 0 10 10 ........................ 1 1 ........................ 10 10 ........................ 0.25 0.5 ........................ 2.5 5 179 Number of recordkeepers Hours per year Non-alternative Facilities (124.510(a)) ........................................................................................ 86 50 4,300 Subtotal recordkeeping burden ............................................................................................ ........................ ........................ 4,300 Reporting Uncompensated Services Report—HRSA–710 Form (124.509(a)) ...................................................................... Application for Compliance Alternatives: Public Facilities (124.513) ............................................ Small Obligation Facilities (124.514(c)) ........................ Charitable Facilities (124.516(c)) .................................. Annual Certification for Compliance Alternatives: Public Facilities (124.509(b)) ........................................ Charitable Facilities (124.509(b)) ................................. Small Obligation Facilities (124.509(c)) ........................ Complaint Information (124.511(a)): Individuals ..................................................................... Facilities ........................................................................ Subtotal reporting burden ............................................. Recordkeeping The total burden for this project is estimated to be 14,678.60 hours. Written comments and recommendations concerning the proposed information collection should be sent within 30 days of this notice to the desk officer for HRSA, either by e-mail to OIRA_submission@omb.eop.gov or by fax to (202) 395–6974. Please direct all correspondence to the ‘‘attention of the desk officer for HRSA.’’ Dated: April 3, 2009. Alexandra Huttinger, Director, Division of Policy Review and Coordination. [FR Doc. E9–8141 Filed 4–8–09; 8:45 am] dwashington3 on PROD1PC60 with NOTICES BILLING CODE 4165–15–P VerDate Nov<24>2008 15:28 Apr 08, 2009 Jkt 217001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC); Notice of Meeting In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Pub. L. 92–463), notice is hereby given of the following meeting: Name: Advisory Committee on Heritable Disorders in Newborns and Children. Date and Time: May 12, 2009, 1 p.m.–5 p.m. EST. Place: Web cast. The ACHDNC will meet on Tuesday, May 12, 2009 from 1 p.m. to 5 p.m. EST. The general public can join the meeting via Webcast by logging onto http:// altarum.na3.acrobat.com/achdnc/; next select ‘‘enter as a guest,’’ type in your full name, and click ‘‘enter room.’’ Participants must also dial the toll free phone number for audio (listen only). The dial-in number is 1 PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 Total hour burden (877) 551–8166; when prompted say the password ‘‘HRSA Genetics’’. Participants should call no later than 12:50 p.m. EST in order for the logistics to be established for participation in the call. If there are technical problems gaining access to the call, please contact Alison Gary, Web Meetings Coordinator, Altarum Institute, telephone (202) 828–5100, or e-mail webmeeting@altarum.org. Meeting Registration: General public participants are asked to register for the conference by going to the meeting Web site at http://events.SignUp4.com/achdnc0509. The registration deadline is Monday, May 11, 2009. Special Accommodations: Attendees requiring special needs such as large print materials or additional special needs may make comments when registering at the Online Web site. Or you may wish to contact Tamar R. Shealy, Senior Meetings Manager, Conference and Meetings Management, Conference, Web and Communication Services, Altarum Institute; telephone (202) 828–5100, or e-mail Tamar Shealy at conferences@altarum.org. Agenda: The meeting will include (1) A presentation of the external review E:\FR\FM\09APN1.SGM 09APN1 dwashington3 on PROD1PC60 with NOTICES Federal Register / Vol. 74, No. 67 / Thursday, April 9, 2009 / Notices workgroup’s preliminary report on the nomination of Krabbe disease to the uniform newborn screening panel, (2) a discussion of the Committee’s draft issue brief for recommending policies to states for the use and storage of newborn screening Residual Blood Spots, and (3) a discussion of the impact of the present economy on State newborn screening program infrastructures. Agenda items are subject to change as priorities dictate. You can also locate the Agenda, presentations, and meeting materials at the home page of the meeting Web site at http://events.SignUp4.com/achdnc0509. Public Comments: Members of the public may present oral comments during the public comment session. Individuals must register at the meeting Web site at http:// events.SignUp4.com/achdnc0509 by Monday, May 11, 2009 to receive via e-mail their assigned presentation time. Groups having similar interests are requested to combine their comments and present them through a single representative. The allocation of time may be adjusted to accommodate the level of expressed interest. Those presenting oral comments are requested to submit their comments in writing for distribution to Committee members by Monday, May 11, 2009. Comments should be submitted to Tamar R. Shealy, Senior Meetings Manager, Conference and Meetings Management, Conference, Web and Communication Services, Altarum Institute; telephone (202) 828–5100, fax (202) 785–3083, or e-mail Tamar Shealy at conferences@altarum.org. For Further Information Contact: Anyone interested in obtaining other relevant information should contact Alaina M. Harris, Maternal and Child Health Bureau, Health Resources and Services Administration, Room 18A–19, Parklawn Building, 5600 Fishers Lane, Rockville, Maryland 20857, Telephone (301) 443–0721, aharris@hrsa.gov. More information on the Advisory Committee is available at http:// www.hrsa.gov/heritabledisorderscommittee/. Supplementary Information: The ACHDNC was chartered originally under Section 1111 of the Public Health Service (PHS) Act, 42 U.S.C. 300b–10 in February 2003 to advise the Secretary of the U.S. Department of Health and Human Services and as amended in the Newborn Screening Saves Lives Act. The Committee is governed by the provisions of Public Law 92–463, as amended (5 U.S.C. App. 2), and 41 CFR part 102–3, which sets forth standards for the formation and use of advisory committees. The ACHDNC is directed to review and report regularly on newborn and childhood screening practices for heritable disorders and to recommend improvements in the national newborn and childhood heritable screening programs. Dated: April 3, 2009. Alexandra Huttinger, Director, Division of Policy Review and Coordination. [FR Doc. E9–8136 Filed ––; 8:45 am] BILLING CODE 4165–15–P VerDate Nov<24>2008 15:28 Apr 08, 2009 Jkt 217001 DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute of Mental Health; Notice of Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of a meeting of the National Advisory Mental Health Council. The meeting will be open to the public as indicated below, with attendance limited to space available. Individuals who plan to attend and need special assistance, such as sign language interpretation or other reasonable accommodations, should notify the Contact Person listed below in advance of the meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Advisory Mental Health Council. Date: May 28–29, 2009. Closed: May 28, 2009, 10:30 a.m. to 5 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, Neuroscience Center, 6001 Executive Boulevard, Conference Room C/D/E, Rockville, MD 20852. Open: May 29, 2009, 8:30 a.m. to 12:30 p.m. Agenda: Presentation of NIMH Director’s report and discussion on NIMH program and policy issues. Place: National Institutes of Health, Building 31, C Wing, 31 Center Drive, 6th Floor, Conference Room 6, Bethesda, MD 20892. Contact Person: Jane A. Steinberg, PhD, Director, Division of Extramural Activities, National Institute of Mental Health, NIH, Neuroscience Center, 6001 Executive Blvd., Room 6154, MSC 9609, Bethesda, MD 20892– 9609, 301–443–5047. Any member of the public interested in presenting oral comments to the committee may notify the Contact Person listed on this notice at least 10 days in advance of the meeting. Interested individuals and representatives of organizations may submit a letter of intent, a brief description of the organization represented, and a short description of the oral presentation. Only one representative of an organization may be allowed to present oral comments and if PO 00000 Frm 00044 Fmt 4703 Sfmt 4703 16219 accepted by the committee, presentations may be limited to five minutes. Both printed and electronic copies are requested for the record. In addition, any interested person may file written comments with the committee by forwarding their statement to the Contact Person listed on this notice. The statement should include the name, address, telephone number and when applicable, the business or professional affiliation of the interested person. In the interest of security, NIH has instituted stringent procedures for entrance onto the NIH campus. All visitor vehicles, including taxicabs, hotel, and airport shuttles will be inspected before being allowed on campus. Visitors will be asked to show one form of identification (for example, a government-issued photo ID, driver’s license, or passport) and to state the purpose of their visit. Information is also available on the Institute’s/Center’s home page: http:// www.nimh.nih.gov/about/advisory-boardsand-groups/namhc/index.shtml where an agenda and any additional information for the meeting will be posted when available. (Catalogue of Federal Domestic Assistance Program Nos. 93.242, Mental Health Research Grants; 93.281, Scientist Development Award, Scientist Development Award for Clinicians, and Research Scientist Award; 93.282, Mental Health National Research Service Awards for Research Training, National Institutes of Health, HHS) Dated: April 2, 2009. Jennifer Spaeth, Director, Office of Federal Advisory Committee Policy. [FR Doc. E9–8015 Filed 4–8–09; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Center for Scientific Review; Notice of Closed Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: Center for Scientific Review Special Emphasis; Panel Member Conflicts: Sensory Neurophysiology. Date: April 13, 2009. E:\FR\FM\09APN1.SGM 09APN1

Agencies

[Federal Register Volume 74, Number 67 (Thursday, April 9, 2009)]
[Notices]
[Pages 16218-16219]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-8136]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Health Resources and Services Administration


Advisory Committee on Heritable Disorders in Newborns and 
Children (ACHDNC); Notice of Meeting

    In accordance with section 10(a)(2) of the Federal Advisory 
Committee Act (Pub. L. 92-463), notice is hereby given of the following 
meeting:

    Name: Advisory Committee on Heritable Disorders in Newborns and 
Children.
    Date and Time: May 12, 2009, 1 p.m.-5 p.m. EST.
    Place: Web cast.
    The ACHDNC will meet on Tuesday, May 12, 2009 from 1 p.m. to 5 
p.m. EST. The general public can join the meeting via Webcast by 
logging onto http://altarum.na3.acrobat.com/achdnc/; next select 
``enter as a guest,'' type in your full name, and click ``enter 
room.'' Participants must also dial the toll free phone number for 
audio (listen only). The dial-in number is 1 (877) 551-8166; when 
prompted say the password ``HRSA Genetics''. Participants should 
call no later than 12:50 p.m. EST in order for the logistics to be 
established for participation in the call. If there are technical 
problems gaining access to the call, please contact Alison Gary, Web 
Meetings Coordinator, Altarum Institute, telephone (202) 828-5100, 
or e-mail webmeeting@altarum.org.
    Meeting Registration: General public participants are asked to 
register for the conference by going to the meeting Web site at 
http://events.SignUp4.com/achdnc0509. The registration deadline is 
Monday, May 11, 2009.
    Special Accommodations: Attendees requiring special needs such 
as large print materials or additional special needs may make 
comments when registering at the Online Web site. Or you may wish to 
contact Tamar R. Shealy, Senior Meetings Manager, Conference and 
Meetings Management, Conference, Web and Communication Services, 
Altarum Institute; telephone (202) 828-5100, or e-mail Tamar Shealy 
at conferences@altarum.org.
    Agenda: The meeting will include (1) A presentation of the 
external review

[[Page 16219]]

workgroup's preliminary report on the nomination of Krabbe disease 
to the uniform newborn screening panel, (2) a discussion of the 
Committee's draft issue brief for recommending policies to states 
for the use and storage of newborn screening Residual Blood Spots, 
and (3) a discussion of the impact of the present economy on State 
newborn screening program infrastructures. Agenda items are subject 
to change as priorities dictate. You can also locate the Agenda, 
presentations, and meeting materials at the home page of the meeting 
Web site at http://events.SignUp4.com/achdnc0509.
    Public Comments: Members of the public may present oral comments 
during the public comment session. Individuals must register at the 
meeting Web site at http://events.SignUp4.com/achdnc0509 by Monday, 
May 11, 2009 to receive via e-mail their assigned presentation time. 
Groups having similar interests are requested to combine their 
comments and present them through a single representative. The 
allocation of time may be adjusted to accommodate the level of 
expressed interest. Those presenting oral comments are requested to 
submit their comments in writing for distribution to Committee 
members by Monday, May 11, 2009. Comments should be submitted to 
Tamar R. Shealy, Senior Meetings Manager, Conference and Meetings 
Management, Conference, Web and Communication Services, Altarum 
Institute; telephone (202) 828-5100, fax (202) 785-3083, or e-mail 
Tamar Shealy at conferences@altarum.org.
    For Further Information Contact: Anyone interested in obtaining 
other relevant information should contact Alaina M. Harris, Maternal 
and Child Health Bureau, Health Resources and Services 
Administration, Room 18A-19, Parklawn Building, 5600 Fishers Lane, 
Rockville, Maryland 20857, Telephone (301) 443-0721, 
aharris@hrsa.gov. More information on the Advisory Committee is 
available at http://www.hrsa.gov/heritabledisorderscommittee/.
    Supplementary Information: The ACHDNC was chartered originally 
under Section 1111 of the Public Health Service (PHS) Act, 42 U.S.C. 
300b-10 in February 2003 to advise the Secretary of the U.S. 
Department of Health and Human Services and as amended in the 
Newborn Screening Saves Lives Act. The Committee is governed by the 
provisions of Public Law 92-463, as amended (5 U.S.C. App. 2), and 
41 CFR part 102-3, which sets forth standards for the formation and 
use of advisory committees. The ACHDNC is directed to review and 
report regularly on newborn and childhood screening practices for 
heritable disorders and to recommend improvements in the national 
newborn and childhood heritable screening programs.

    Dated: April 3, 2009.
Alexandra Huttinger,
Director, Division of Policy Review and Coordination.
[FR Doc. E9-8136 Filed --; 8:45 am]
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