Secretary's Advisory Committee on Heritable Disorders in Newborns and Children; Notice of Meeting, 17140 [2011-7166]
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17140
Federal Register / Vol. 76, No. 59 / Monday, March 28, 2011 / Notices
out of an electronic medical record, and
the purchase and use of a mobile
medical van.
SPHC is an experienced provider of
care and has a demonstrated record of
compliance with Health Center Program
statutory and regulatory requirements
and is located in the same geographical
area. The transfer of the ARRA Capital
Improvement Project funds will ensure
that critical primary health care services
continue and remain available to the
low-income, underserved homeless
patients with no interruption in services
to the target population.
FOR FURTHER INFORMATION CONTACT:
Marquita Cullom-Scott via e-mail at
MCullom-Scott@hrsa.gov or 301–594–
4300.
Dated: March 23, 2011.
Mary K. Wakefield,
Administrator.
[FR Doc. 2011–7248 Filed 3–25–11; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Secretary’s Advisory Committee on
Heritable Disorders in Newborns and
Children; Notice of Meeting
Emcdonald on DSK2BSOYB1PROD with NOTICES
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: Secretary’s Advisory Committee on
Heritable Disorders in Newborns and
Children.
Dates and Times: May 5, 2011, 9:30 a.m.
to 5 p.m., May 6, 2011, 8:30 a.m. to 3:30 p.m.
Place: Renaissance Washington, DC,
Dupont Circle Hotel, 1143 New Hampshire
Avenue, NW., Washington, DC 20037.
Status: The meeting will be open to the
public with attendance limited to space
availability. Participants are asked to register
for the meeting by going to the registration
Web site at
https://altarum.cvent.com/event/
SACHDNC052011. The registration deadline
is Tuesday, May 3, 2011. Individuals who
need special assistance, such as sign
language interpretation or other reasonable
accommodations should indicate their needs
on the registration Web site. The deadline for
special accommodation requests is Friday,
April 29, 2011. If there are technical
problems gaining access to the Web site,
please contact Maureen Ball, Meetings
Coordinator at conferences@altarum.org.
Purpose: The Secretary’s Advisory
Committee on Heritable Disorders in
Newborns and Children (Advisory
Committee) was established to advise and
guide the Secretary regarding the most
appropriate application of universal newborn
VerDate Mar<15>2010
17:14 Mar 25, 2011
Jkt 223001
screening tests, technologies, policies,
guidelines and programs for effectively
reducing morbidity and mortality in
newborns and children having or at risk for
heritable disorders. The Advisory Committee
as authorized under the Public Health
Service Act 42 U.S.C. 300b–10, and amended
in the Newborn Screening Saves Lives Act of
2008, also provides advice and
recommendations concerning the grants and
projects authorized under the Public Health
Service Act, 42 U.S.C. 300b–8, (Heritable
Disorders Program) as amended in the
Newborn Screening Saves Lives Act of 2008.
Agenda: The meeting will include: (1) A
presentation of the External Review
Workgroup’s final report on the nomination
of Hyperbilirubinemia to the Advisory
Committee’s recommended uniform
screening panel; (2) an update from the
Evidence Evaluation Methods workgroup;
and (3) presentations on the continued work
and reports of the Advisory Committee’s
subcommittees on laboratory standards and
procedures, follow-up and treatment, and
education and training. Proposed agenda
items are subject to change as priorities
dictate. You can locate the Agenda,
Committee Roster and Charter, presentations,
and meeting materials at the home page of
the Advisory Committee’s Web site at https://
www.hrsa.gov/heritabledisorderscommittee/.
Public Comments: Members of the public
can submit written comments and/or present
oral comments during the public comment
periods of the meeting, which are scheduled
for both days of the meeting. Those
individuals who want to make oral
comments are requested to register online by
Tuesday, May 3, 2011 at https://
altarum.cvent.com/event/SACHDNC052011.
Requests should contain the name, address,
telephone number, and any professional or
business affiliation of the person desiring to
make an oral presentation. Groups having
similar interests are requested to combine
their comments and present them through a
single representative. Written comments
should be emailed no later than Tuesday,
May 3, 2011, for consideration. Written
comments should contain the name, address,
telephone number, and any professional or
business affiliation of the author. Submit
written comments to Maureen Ball, Meetings
Coordinator, Conference and Meetings
Management, Altarum Institute, 1200 18th
Street, NW., Suite 700, Washington, DC
20036, telephone: 202 828–5100; fax: 202
785–3083, or e-mail:
conferences@altarum.org.
Contact Person: Anyone interested in
obtaining other relevant information should
write or 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 https://mchb.hrsa.gov/
heritabledisorderscommittee.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: March 22, 2011.
Wendy Ponton,
Director, Office of Management.
National Institute on Alcohol Abuse
and Alcoholism; Notice of Closed
Meeting
[FR Doc. 2011–7166 Filed 3–25–11; 8:45 am]
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
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National Institutes of Health
National Center for Complementary &
Alternative Medicine; 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: National Center for
Complementary and Alternative Medicine
Special Emphasis Panel; Neurophysiological
and Pain Management with CAM Treatments.
Date: April 5, 2011.
Time: 1 p.m. to 4 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, Two
Democracy Plaza, 6707 Democracy
Boulevard, Bethesda, MD 20892, (Telephone
Conference Call)
Contact Person: Hungyi Shau, PhD,
Scientific Review Officer, National Center for
Complementary and Alternative Medicine,
National Institutes of Health, 6707
Democracy Boulevard, Suite 401, Bethesda,
MD 20892, 301–402–1030,
Hungyi.Shau@nih.gov.
This meeting is being published less than
15 days prior to the meeting date due to
scheduling conflicts.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.213, Research and Training
in Complementary and Alternative Medicine,
National Institutes of Health, HHS)
Dated: March 21, 2011.
Jennifer S. Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2011–7199 Filed 3–25–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
E:\FR\FM\28MRN1.SGM
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Agencies
[Federal Register Volume 76, Number 59 (Monday, March 28, 2011)]
[Notices]
[Page 17140]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-7166]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Secretary's Advisory Committee on Heritable Disorders in Newborns
and Children; 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: Secretary's Advisory Committee on Heritable Disorders in
Newborns and Children.
Dates and Times: May 5, 2011, 9:30 a.m. to 5 p.m., May 6, 2011,
8:30 a.m. to 3:30 p.m.
Place: Renaissance Washington, DC, Dupont Circle Hotel, 1143 New
Hampshire Avenue, NW., Washington, DC 20037.
Status: The meeting will be open to the public with attendance
limited to space availability. Participants are asked to register
for the meeting by going to the registration Web site at https://altarum.cvent.com/event/SACHDNC052011. The registration deadline is
Tuesday, May 3, 2011. Individuals who need special assistance, such
as sign language interpretation or other reasonable accommodations
should indicate their needs on the registration Web site. The
deadline for special accommodation requests is Friday, April 29,
2011. If there are technical problems gaining access to the Web
site, please contact Maureen Ball, Meetings Coordinator at
conferences@altarum.org.
Purpose: The Secretary's Advisory Committee on Heritable
Disorders in Newborns and Children (Advisory Committee) was
established to advise and guide the Secretary regarding the most
appropriate application of universal newborn screening tests,
technologies, policies, guidelines and programs for effectively
reducing morbidity and mortality in newborns and children having or
at risk for heritable disorders. The Advisory Committee as
authorized under the Public Health Service Act 42 U.S.C. 300b-10,
and amended in the Newborn Screening Saves Lives Act of 2008, also
provides advice and recommendations concerning the grants and
projects authorized under the Public Health Service Act, 42 U.S.C.
300b-8, (Heritable Disorders Program) as amended in the Newborn
Screening Saves Lives Act of 2008.
Agenda: The meeting will include: (1) A presentation of the
External Review Workgroup's final report on the nomination of
Hyperbilirubinemia to the Advisory Committee's recommended uniform
screening panel; (2) an update from the Evidence Evaluation Methods
workgroup; and (3) presentations on the continued work and reports
of the Advisory Committee's subcommittees on laboratory standards
and procedures, follow-up and treatment, and education and training.
Proposed agenda items are subject to change as priorities dictate.
You can locate the Agenda, Committee Roster and Charter,
presentations, and meeting materials at the home page of the
Advisory Committee's Web site at https://www.hrsa.gov/heritabledisorderscommittee/.
Public Comments: Members of the public can submit written
comments and/or present oral comments during the public comment
periods of the meeting, which are scheduled for both days of the
meeting. Those individuals who want to make oral comments are
requested to register online by Tuesday, May 3, 2011 at https://altarum.cvent.com/event/SACHDNC052011. Requests should contain the
name, address, telephone number, and any professional or business
affiliation of the person desiring to make an oral presentation.
Groups having similar interests are requested to combine their
comments and present them through a single representative. Written
comments should be emailed no later than Tuesday, May 3, 2011, for
consideration. Written comments should contain the name, address,
telephone number, and any professional or business affiliation of
the author. Submit written comments to Maureen Ball, Meetings
Coordinator, Conference and Meetings Management, Altarum Institute,
1200 18th Street, NW., Suite 700, Washington, DC 20036, telephone:
202 828-5100; fax: 202 785-3083, or e-mail: conferences@altarum.org.
Contact Person: Anyone interested in obtaining other relevant
information should write or 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 https://mchb.hrsa.gov/heritabledisorderscommittee.
Dated: March 22, 2011.
Wendy Ponton,
Director, Office of Management.
[FR Doc. 2011-7166 Filed 3-25-11; 8:45 am]
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