National Advisory Committee on Rural Health and Human Services; Notice of Meeting, 160-161 [2010-33062]
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Federal Register / Vol. 76, No. 1 / Monday, January 3, 2011 / Notices
manufacturer to promote participation.
The third factor is that some States have
initiated PT requirements, deeming this
quality check of sufficient importance to
mandate successful participation as a
requisite for Medicaid reimbursement.
This State-level action illustrates the
importance of this PT participation, and
may be the beginning of a trend that will
serve to increase participation even
more.
The University of Wisconsin will use
these funds to initiate an orderly
closeout of HRSA-funded activities
which clearly falls within the purview
of the Centers for Disease Control and
Prevention’s ‘‘Preventing Lead Poisoning
in Young Children’’ initiative at their
National Center for Environmental
Health. This extension with funding
will also accord the University of
Wisconsin and the Center to solicit
recommendations from the CDC’s
Advisory Committee on Childhood Lead
Poisoning Prevention with respect to
future funding for this activity.
FOR FURTHER INFORMATION CONTACT:
David Heppel, M.D., Director, Division
of Child, Adolescent and Family Health,
Maternal and Child Health Bureau,
Health Resources and Services
Administration, 5600 Fishers Lane,
Room 18A–30, Rockville, MD 20857;
301–443–2250; dheppel@hrsa.gov.
Authority: Section 501(c)(1) of the Social
Security Act, as amended.
jlentini on DSKJ8SOYB1PROD with NOTICES
the U.S., and is unfortunately overrepresented in minority, immigrant, and
low socio-economic populations. The
proper detection and treatment of lead
poisoning relies entirely on the accurate
and precise measurement of blood lead
concentration. EP is utilized as an
adjunct test to indicate the extent and
duration of lead exposure, as well as the
detection of iron deficiency, another
pediatric health issue. Proficiency
testing (PT) is a proven method for
assuring and improving laboratory test
accuracy. This program has costeffectively provided monthly PT and
other lab quality improvement tools to
nearly 600 laboratories across the U.S.
and beyond. Of note, the primary focus
of the program over the last few years
has been the integration of new and
usually inexperienced participants into
the program. An enrollment boom has
been fueled by proliferation of the CLIAwaived LeadCare II point of care testing
instrument. In the three years since its
introduction, LeadCare II enrollment
has grown from zero to 300 laboratories,
comprising approximately 40 percent of
all participants. Continued participation
increases, and the fact that those
increases are nearly totally comprised of
LeadCare II users, represent both a
public health success and a challenge
for this program. Since its introduction
in early 2007, over 300 of these
laboratories have enrolled for PT,
swelling program participation to 800
laboratories.
SUPPLEMENTARY INFORMATION:
Intended Recipients of the Award:
University of Wisconsin, Laboratory of
Hygiene, Madison, Wisconsin.
Amount of the Non-Competitive
Supplemental Funding: $250,000.
Health Resources and Services
Administration
CFDA Number: 93.110.
Proposed Project Period: January 1,
2008–October 31, 2011.
Justification for Exception to
Competition:
The participation of large numbers of
these labs in voluntary proficiency was
by design, and represents a public
health success by assuring blood lead
screening accuracy where there would
otherwise be no evaluation. Three
factors contribute to this. First, is the
HRSA support of this program, which
has been increased to accommodate the
additional labs.
This support allows laboratories to
participate at no cost, a vital
consideration for voluntary participants.
The second factor is the effort of the
NBLPT Program to integrate the new
technology shortly after it became
available, and collaboration with the
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15:48 Dec 30, 2010
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Dated: December 23, 2010.
Mary K. Wakefield,
Administrator.
[FR Doc. 2010–33063 Filed 12–30–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Advisory Committee on Rural
Health and Human Services; Notice of
Meeting
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), announcement is
made of the following National
Advisory body scheduled to meet
during the month of February 2011.
The National Advisory committee on
Rural Health will convene its sixtyseventh meeting in the time and place
specified below:
Name: National Advisory Committee
on Rural Health and Human Services.
Dates and Times:
February 23, 2011, 8:45 a.m.–5 p.m.
February 24, 2011, 8:45 a.m.–4 p.m.
February 25, 2011, 8:45 a.m.–11:15 a.m.
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Place: Omni Shoreham Hotel, 2500
Calvert Street, NW., Washington, DC
20008.
Phone: (202) 234–0700.
Status: The meeting will be open to
the public.
Purpose: The National Advisory
Committee on Rural Health and Human
Services provides advice and
recommendations to the Secretary with
respect to the delivery, research,
development and administration of
health and human services in rural
areas.
Agenda: Wednesday morning at 9
a.m. the meeting will be called to order
by the Chairperson of the Committee,
the Honorable Ronnie Musgrove. There
will be an update from officials from the
Department of Health and Human
Services. This will be followed by a
series of panel presentations on key
provisions from the Affordable Care Act
(ACA). The Committee will be
examining the rural implications of
several provisions from the ACA,
including health insurance exchanges,
the Maternal and Early Childhood Home
Visitation program and the Community
Living Assistance, Services and Support
program. The day will conclude with a
period of public comment at
approximately 4:30 p.m.
Thursday morning at 9 a.m. the
Committee will continue to hear panel
presentations on ACA-related
provisions and will then break into
subcommittees on each of those topics
for further discussion. The day will
conclude with a period of public
comment at approximately 4:30 p.m.
Friday morning at 9 a.m. the
Committee will summarize key findings
from the meeting and develop a work
plan for the next quarter and the June
meeting.
FOR FURTHER INFORMATION CONTACT:
Thomas Morris, MPA, Executive
Secretary, National Advisory Committee
on Rural Health and Human Services,
Health Resources and Services
Administration, Parklawn Building,
Room 10B–45, 5600 Fishers Lane,
Rockville, MD 20857, Telephone (301)
443–0835, Fax (301) 443–2803.
Persons interested in attending any
portion of the meeting should contact
Tish Scolnick at the Office of Rural
Health Policy (ORHP) via Telephone at
(301) 443–0835, or by e-mail at
nscolnick@hrsa.gov. The Committee
meeting agenda will be posted on
ORHP’s Web site https://
www.ruralhealth.hrsa.gov.
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03JAN1
Federal Register / Vol. 76, No. 1 / Monday, January 3, 2011 / Notices
Dated: December 27, 2010,,
Robert Hendricks,
Director, Division of Policy and Information
Coordination.
[FR Doc. 2010–33062 Filed 12–30–10; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Eunice Kennedy Shriver National
Institute of Child Health & Human
Development; 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 concept meeting,
proposals and the discussions could
disclose confidential trade secrets or
commercial property such as patentable
material, and personal information
concerning individuals associated with
the contract proposals, the disclosure of
which would constitute a clearly
unwarranted invasion of personal
privacy.
jlentini on DSKJ8SOYB1PROD with NOTICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Substance Abuse and Mental Health
Services Administration
Eunice Kennedy Shriver National
Institute of Child Health & Human
Development; Notice of Closed
Meeting
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Name of Committee: National Institute of
Child Health and Human Development
Special Emphasis Panel. Contraceptive
Clinical Trials Network.
Date: January 12, 2011.
Time: 1 p.m. to 3 p.m.
Agenda: To review and evaluate concept
review.
Place: National Institutes of Health, 6100
Executive Boulevard, Room 2A01, Rockville,
MD 20852. (Telephone Conference Call).
Contact Person: Sathasiva B. Kandasamy,
PhD, Scientific Review Administrator,
Division of Scientific Review, National
Institute of Child Health and Human
Development, 6100 Executive Boulevard,
Rockville, Md 20892–9304. (301) 435–6680.
skandasa@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.864, Population Research;
93.865, Research for Mothers and Children;
93.929, Center for Medical Rehabilitation
Research; 93.209, Contraception and
Infertility Loan Repayment program, National
Institutes of Health, HHS)
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 contract proposals and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the contract
proposals, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Child Health and Human Development
Special Emphasis Panel.
Date: January 10, 2011.
Time: 12:45 p.m. to 3 p.m.
Agenda: To review and evaluate contract
proposals.
Place: National Institutes of Health, 6100
Executive Boulevard, Room 2A01, Rockville,
MD 20852. (Telephone Conference).
Contact Person: Sathasiva B. Kandasamy,
PhD, Scientific Review Administrator,
Division of Scientific Review, National
Institute of Child Health and Human
Development, 6100 Executive Boulevard,
Rockville, MD 20892–9304. (301) 435–6680.
skandasa@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.864, Population Research;
93.865, Research for Mothers and Children;
93.929, Center for Medical Rehabilitation
Research; 93.209, Contraception and
Infertility Loan Repayment Program, National
Institutes of Health, HHS)
Dated: December 27, 2010.
Jennifer S. Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2010–33068 Filed 12–30–10; 8:45 am]
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Dated: December 27, 2010.
Jennifer S. Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2010–33067 Filed 12–30–10; 8:45 am]
BILLING CODE 4140–01–P
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Current List of Laboratories and
Instrumented Initial Testing Facilities
Which Meet Minimum Standards To
Engage in Urine Drug Testing for
Federal Agencies
AGENCY: Substance Abuse and Mental
Health Services Administration, HHS.
ACTION: Notice.
SUMMARY: The Department of Health and
Human Services (HHS) notifies Federal
agencies of the Laboratories and
Instrumented Initial Testing Facilities
(IITF) currently certified to meet the
standards of the Mandatory Guidelines
for Federal Workplace Drug Testing
Programs (Mandatory Guidelines). The
Mandatory Guidelines were first
published in the Federal Register on
April 11, 1988 (53 FR 11970), and
subsequently revised in the Federal
Register on June 9, 1994 (59 FR 29908);
September 30, 1997 (62 FR 51118);
April 13, 2004 (69 FR 19644); November
25, 2008 (73 FR 71858); December 10,
2008 (73 FR 75122); and on April 30,
2010 (75 FR 22809).
A notice listing all currently certified
Laboratories and Instrumented Initial
Testing Facilities (IITF) is published in
the Federal Register during the first
week of each month. If any Laboratory/
IITF’s certification is suspended or
revoked, the Laboratory/IITF will be
omitted from subsequent lists until such
time as it is restored to full certification
under the Mandatory Guidelines.
If any Laboratory/IITF has withdrawn
from the HHS National Laboratory
Certification Program (NLCP) during the
past month, it will be listed at the end
and will be omitted from the monthly
listing thereafter.
This notice is also available on the
Internet at https://
www.workplace.samhsa.gov and https://
www.drugfreeworkplace.gov.
FOR FURTHER INFORMATION CONTACT: Mrs.
Giselle Hersh, Division of Workplace
Programs, SAMHSA/CSAP, Room 2–
1042, One Choke Cherry Road,
Rockville, Maryland 20857; 240–276–
2600 (voice), 240–276–2610 (fax).
SUPPLEMENTARY INFORMATION: The
Mandatory Guidelines were initially
developed in accordance with Executive
Order 12564 and section 503 of Public
Law 100–71. The ‘‘Mandatory
Guidelines for Federal Workplace Drug
Testing Programs’’, as amended in the
revisions listed above, requires {or set}
strict standards that Laboratories and
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Agencies
[Federal Register Volume 76, Number 1 (Monday, January 3, 2011)]
[Notices]
[Pages 160-161]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-33062]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
National Advisory Committee on Rural Health and Human Services;
Notice of Meeting
In accordance with section 10(a)(2) of the Federal Advisory
Committee Act (Pub. L. 92-463), announcement is made of the following
National Advisory body scheduled to meet during the month of February
2011.
The National Advisory committee on Rural Health will convene its
sixty-seventh meeting in the time and place specified below:
Name: National Advisory Committee on Rural Health and Human
Services.
Dates and Times:
February 23, 2011, 8:45 a.m.-5 p.m.
February 24, 2011, 8:45 a.m.-4 p.m.
February 25, 2011, 8:45 a.m.-11:15 a.m.
Place: Omni Shoreham Hotel, 2500 Calvert Street, NW., Washington,
DC 20008.
Phone: (202) 234-0700.
Status: The meeting will be open to the public.
Purpose: The National Advisory Committee on Rural Health and Human
Services provides advice and recommendations to the Secretary with
respect to the delivery, research, development and administration of
health and human services in rural areas.
Agenda: Wednesday morning at 9 a.m. the meeting will be called to
order by the Chairperson of the Committee, the Honorable Ronnie
Musgrove. There will be an update from officials from the Department of
Health and Human Services. This will be followed by a series of panel
presentations on key provisions from the Affordable Care Act (ACA). The
Committee will be examining the rural implications of several
provisions from the ACA, including health insurance exchanges, the
Maternal and Early Childhood Home Visitation program and the Community
Living Assistance, Services and Support program. The day will conclude
with a period of public comment at approximately 4:30 p.m.
Thursday morning at 9 a.m. the Committee will continue to hear
panel presentations on ACA-related provisions and will then break into
subcommittees on each of those topics for further discussion. The day
will conclude with a period of public comment at approximately 4:30
p.m.
Friday morning at 9 a.m. the Committee will summarize key findings
from the meeting and develop a work plan for the next quarter and the
June meeting.
FOR FURTHER INFORMATION CONTACT: Thomas Morris, MPA, Executive
Secretary, National Advisory Committee on Rural Health and Human
Services, Health Resources and Services Administration, Parklawn
Building, Room 10B-45, 5600 Fishers Lane, Rockville, MD 20857,
Telephone (301) 443-0835, Fax (301) 443-2803.
Persons interested in attending any portion of the meeting should
contact Tish Scolnick at the Office of Rural Health Policy (ORHP) via
Telephone at (301) 443-0835, or by e-mail at nscolnick@hrsa.gov. The
Committee meeting agenda will be posted on ORHP's Web site https://www.ruralhealth.hrsa.gov.
[[Page 161]]
Dated: December 27, 2010,,
Robert Hendricks,
Director, Division of Policy and Information Coordination.
[FR Doc. 2010-33062 Filed 12-30-10; 8:45 am]
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