Advisory Committee on Heritable Disorders in Newborns and Children, 2554-2555 [2010-671]
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medicine; unmet needs in diagnostic
testing for women with cardiovascular
disease; issues of cardiovascular
prevention across the lifespan with an
emphasis on gender and underserved
populations; and women’s careers in the
biomedical sciences. On February 17,
the morning session will be devoted to
reports by the working group co-chairs
regarding the recommendations
emerging from working group
deliberations on the previous day. The
meeting will adjourn at 12:15 p.m. on
February 17.
Public Testimony
ORWH invites individuals with an
interest in research related to women’s
health to provide written and/or oral
testimony on these topics and/or on
issues related to the sustained
advancement of women in various
biomedical careers. Due to time
constraints, only one representative
from an organization or professional
specialty group may submit oral
testimony. Individuals not representing
an organized entity but a personal point
of view are similarly invited to present
written and/or oral testimony. A letter
of intent to present oral testimony is
necessary and should be sent
electronically to https://
www.orwhmeetings.com/
movingintothefuture/Emory or by mail
to Ms. Jory Barone, Educational
Services, Inc., 4350 East West Highway,
Suite 1100, Bethesda, MD 20814, no
later than midnight February 1, 2010.
The date of receipt of the
communication will establish the order
of those selected to give oral testimony
at the February meeting.
Those wishing to present oral
testimony are also asked to submit a
written form of their testimony that is
limited to a maximum of 10 pages,
double spaced, 12-point font, and
should include a brief description of the
organization. Electronic submission to
the above Web site is preferred;
however, for those who do not have
access to electronic means, written
testimony, bound by the restrictions
previously noted and postmarked no
later than February 1, 2010, can be
mailed to Ms. Jory Barone at the above
address. All written presentations must
meet the established page limitations.
Submissions exceeding this limit will
not be accepted and will be returned.
Oral testimony of this material at the
meeting will be limited to no more than
5–6 minutes in length.
Because of time constraints for oral
testimony, testifiers may not be able to
present the complete information as it is
contained in their written form
submitted for inclusion in the public
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record for the meeting. Therefore,
testifiers are requested to summarize the
major points of emphasis from the
written testimony not to exceed 6
minutes of oral testimony. Those
individuals and/or organizations who
have indicated that they will present
oral testimony at the meeting in Atlanta,
will be notified prior to the meeting
regarding the approximate time for their
oral presentation.
Individuals and organizations wishing
to provide written statements only
should send a copy of their statements,
electronically or by mail, to the above
Web site or address by February 1, 2010.
Written testimony received by that date
will be made available at the February
16–17 meeting.
Logistics questions related to the
meeting should be addressed to Ms. Jory
Barone, joryb@esi-dc.com at ESI, while
program-specific questions should be
addressed to Dr. Nanette K. Wenger at
the Emory University School of
Medicine, Atlanta, 404–616–4420,
nwenger@emory.edu.
The resulting report to the ORWH and
the NIH will ensure that women’s health
research in the coming decade
continues to support a vigorous research
agenda incorporating the latest advances
in technology and cutting edge science
in support of women’s cardiovascular
health.
Dated: January 8, 2010.
Francis S. Collins,
Director, National Institutes of Health.
[FR Doc. 2010–665 Filed 1–14–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Advisory Committee on Heritable
Disorders in Newborns and Children
AGENCY: Health Resources and Services
Administration (HRSA), HHS.
ACTION: Notice of Request for
Nominations.
SUMMARY: The Health Resources and
Services Administration (HRSA) is
requesting nominations to fill three (3)
vacancies on the Secretary’s Advisory
Committee on Heritable Disorders in
Newborns and Children.
Authority: Section 1111 of the Public
Health Service (PHS) Act, 42 U.S.C. 300b–10,
as amended in the Newborn Screening Saves
Lives Act of 2008 (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
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for the formation and use of advisory
committees.
DATES: The agency must receive
nominations on or before May 1, 2010.
ADDRESSES: All nominations are to be
submitted to Michele A. Lloyd-Puryear,
M.D., PhD, Designated Federal Official
and Executive Secretary, Advisory
Committee on Heritable Disorders in
Newborns and Children, and Chief,
Genetic Services Branch, Maternal and
Child Health Bureau, Health Resources
and Services Administration, Room
18A–19, Parklawn Building, 5600
Fishers Lane, Rockville, Maryland
20857. E-mailed nominations can be
sent to Screening@hrsa.hhs.gov.
FOR FURTHER INFORMATION CONTACT: Ms.
Alaina Harris, Genetic Services Branch,
Maternal and Child Health Bureau,
HRSA, at aharris@hrsa.gov or (301)
443–1080. A copy of the Committee
Charter and list of the current
membership can be obtained by
contacting Ms. Harris or by accessing
the Advisory Committee Web site at
https://hrsa.gov/
heritabledisorderscommittee.
SUPPLEMENTARY INFORMATION: The
Secretary’s ACHDNC is chartered under
section 1111 of the Public Health
Service (PHS) Act, 42 U.S.C. 300b–10,
as amended by the Newborn Screening
Saves Lives Act 2008 (Act). The
Committee was established in February
2003 to advise the Secretary of the U.S.
Department of Health and Human
Services. 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.
The Committee is 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. In addition, the
Committee provides advice and
recommendations to the Secretary
concerning the grants and projects
authorized under section 1109 and
technical information to develop
policies and priorities for this Program
that will enhance the ability of the State
and local health agencies to provide for
newborn and child screening,
counseling and health care services for
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jlentini on DSKJ8SOYB1PROD with NOTICES
Federal Register / Vol. 75, No. 10 / Friday, January 15, 2010 / Notices
newborns and children having or at risk
for heritable disorders.
Specifically, HRSA is requesting
nominations for three (3) voting
members to serve on the Committee.
Members shall be selected from
medical, technical, public health or
scientific professionals with special
expertise in the field of heritable
disorders or in providing screening,
counseling, testing or specialty services
for newborns and children at risk for
heritable disorders and from members of
the public having special expertise
about or concern with heritable
disorders.
The individuals selected for
appointment to the Committee can be
invited to serve for overlapping terms of
up to 4 years. However, any member
appointed to fill a vacancy of an
unexpired term shall be appointed for
the remainder of such term. Members
may serve after the expiration of their
term until their successors have taken
office. Terms of more than 2 years are
contingent upon the renewal of the
Committee by appropriate action prior
to its expiration. Members who are not
Federal employees will receive a
stipend for each day they are engaged in
the performance of their duties as
members of the Committee. Members
shall receive per diem and travel
expenses as authorized by section 5
U.S.C. 5703 for persons employed
intermittently in Government service.
Members who are officers or employees
of the United States Government shall
not receive compensation for service on
the Committee. Nominees will be
invited to serve beginning from October
1, 2010.
Nominations should be typewritten.
The following information should be
included in the package of material
submitted for each individual being
nominated for consideration: (1) A letter
of nomination that clearly states the
name and affiliation of the nominee, the
basis for the nomination (i.e., specific
attributes which qualify the nominee for
service in this capacity), and a statement
that the nominee is willing to serve as
a member of the Committee and appears
to have no conflict of interest that
would preclude the Committee
membership—potential candidates will
be asked to provide detailed information
concerning consultancies, research
grants, or contracts to permit evaluation
of possible sources of conflicts of
interest; (2) the nominator’s name,
address, and daytime telephone
number, and the home/or work address,
telephone number, and e-mail address
of the individual being nominated; and
(3) a current copy of the nominee’s
VerDate Nov<24>2008
17:34 Jan 14, 2010
Jkt 220001
curriculum vitae. Please submit
nominations no later than May 1, 2010.
To the extent practicable, members of
the Committee should have expertise in
dealing with heritable disorders and
genetic diseases that affect the racial
and ethnic and geographical diversity of
newborns served by the State newborn
screening programs. The Department of
Health and Human Services will ensure
that the membership of the Committee
reflects an equitable geographical and
gender distribution, provided that the
effectiveness of the Committee would
not be impaired. Appointments shall be
made without discrimination on the
basis of age, ethnicity, gender, sexual
orientation, and cultural, religious, or
socioeconomic status.
Dated: January 11, 2010.
Mary K. Wakefield,
Administrator.
[FR Doc. 2010–671 Filed 1–14–10; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HOMELAND
SECURITY
[Docket No. DHS–2009–0158]
Homeland Security Science and
Technology Advisory Committee
Science and Technology
Directorate, DHS.
ACTION: Committee management; Notice
of closed Federal Advisory Committee
meeting.
AGENCY:
SUMMARY: The Homeland Security
Science and Technology Advisory
Committee will meet January 26–28,
2010, at the Department of Homeland
Security, 1120 Vermont Ave., NW.,
Washington, DC. This meeting will be
closed to the public.
DATES: The Homeland Security Science
and Technology Advisory Committee
will meet January 26, 2010, from 9 a.m.
to 5 p.m., January 27, 2010, from 9 a.m.
to 5 p.m. and on January 28, 2010, from
8 a.m. to 11 a.m.
ADDRESSES: The meeting will be held at
the Department of Homeland Security,
1120 Vermont Ave., NW., Washington,
DC. Requests to have written material
distributed to each member of the
committee prior to the meeting should
reach the contact person at the address
below by Friday, January 8, 2010. Send
written material to Ms. Tiwanda Burse,
Science and Technology Directorate,
Department of Homeland Security, 245
Murray Lane, Bldg. 410, Washington,
DC 20528. Comments must be identified
by DHS–2009–0158 and may be
submitted by one of the following
methods:
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• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• E-mail: HSSTAC@dhs.gov. Include
the docket number in the subject line of
the message.
• Fax: 202–254–6173.
• Mail: Ms. Tiwanda Burse, Science
and Technology Directorate, Department
of Homeland Security, 245 Murray
Lane, Bldg. 410, Washington, DC 20528.
Instructions: All submissions received
must include the words ‘‘Department of
Homeland Security’’ and the docket
number for this action. Comments
received will be posted without
alteration at https://www.regulations.gov,
including any personal information
provided.
Docket: For access to the docket to
read background documents or
comments received by the (committee
name), go to https://www.regulations.gov.
FOR FURTHER INFORMATION CONTACT: Ms.
Tiwanda Burse, Science and
Technology Directorate, Department of
Homeland Security, 245 Murray Lane,
Bldg. 410, Washington, DC 20528, 202–
254–6877.
Notice of
this meeting is given under the Federal
Advisory Committee Act, 5 U.S.C. App.
(Pub. L. 92–463).
At this meeting, the Committee will
receive sensitive and classified (Top
Secret-level) briefings and presentations
regarding relationships between Science
& Technology and selected Defense
related topics concerning matters
sensitive to homeland security.
Basis for Closure: In accordance with
Section 10(d) of the Federal Advisory
Committee Act, it has been determined
that the Homeland Security Science and
Technology Advisory Committee
meeting concerns sensitive Homeland
Security information and classified
matters within the meaning of 5 U.S.C.
552b(c)(1) and (c)(9)(B) which, if
prematurely disclosed, would
significantly jeopardize national
security and frustrate implementation of
proposed agency actions and that,
accordingly, the portion of the meeting
that concerns these issues will be closed
to the public.
SUPPLEMENTARY INFORMATION:
Dated: January 7, 2010.
Tara O’Toole,
Under Secretary for Science and Technology.
[FR Doc. 2010–737 Filed 1–14–10; 8:45 am]
BILLING CODE 9910–9F–P
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Agencies
[Federal Register Volume 75, Number 10 (Friday, January 15, 2010)]
[Notices]
[Pages 2554-2555]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-671]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Advisory Committee on Heritable Disorders in Newborns and
Children
AGENCY: Health Resources and Services Administration (HRSA), HHS.
ACTION: Notice of Request for Nominations.
-----------------------------------------------------------------------
SUMMARY: The Health Resources and Services Administration (HRSA) is
requesting nominations to fill three (3) vacancies on the Secretary's
Advisory Committee on Heritable Disorders in Newborns and Children.
Authority: Section 1111 of the Public Health Service (PHS) Act,
42 U.S.C. 300b-10, as amended in the Newborn Screening Saves Lives
Act of 2008 (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.
DATES: The agency must receive nominations on or before May 1, 2010.
ADDRESSES: All nominations are to be submitted to Michele A. Lloyd-
Puryear, M.D., PhD, Designated Federal Official and Executive
Secretary, Advisory Committee on Heritable Disorders in Newborns and
Children, and Chief, Genetic Services Branch, Maternal and Child Health
Bureau, Health Resources and Services Administration, Room 18A-19,
Parklawn Building, 5600 Fishers Lane, Rockville, Maryland 20857. E-
mailed nominations can be sent to Screening@hrsa.hhs.gov.
FOR FURTHER INFORMATION CONTACT: Ms. Alaina Harris, Genetic Services
Branch, Maternal and Child Health Bureau, HRSA, at aharris@hrsa.gov or
(301) 443-1080. A copy of the Committee Charter and list of the current
membership can be obtained by contacting Ms. Harris or by accessing the
Advisory Committee Web site at https://hrsa.gov/heritabledisorderscommittee.
SUPPLEMENTARY INFORMATION: The Secretary's ACHDNC is chartered under
section 1111 of the Public Health Service (PHS) Act, 42 U.S.C. 300b-10,
as amended by the Newborn Screening Saves Lives Act 2008 (Act). The
Committee was established in February 2003 to advise the Secretary of
the U.S. Department of Health and Human Services. 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.
The Committee is 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. In addition, the Committee
provides advice and recommendations to the Secretary concerning the
grants and projects authorized under section 1109 and technical
information to develop policies and priorities for this Program that
will enhance the ability of the State and local health agencies to
provide for newborn and child screening, counseling and health care
services for
[[Page 2555]]
newborns and children having or at risk for heritable disorders.
Specifically, HRSA is requesting nominations for three (3) voting
members to serve on the Committee. Members shall be selected from
medical, technical, public health or scientific professionals with
special expertise in the field of heritable disorders or in providing
screening, counseling, testing or specialty services for newborns and
children at risk for heritable disorders and from members of the public
having special expertise about or concern with heritable disorders.
The individuals selected for appointment to the Committee can be
invited to serve for overlapping terms of up to 4 years. However, any
member appointed to fill a vacancy of an unexpired term shall be
appointed for the remainder of such term. Members may serve after the
expiration of their term until their successors have taken office.
Terms of more than 2 years are contingent upon the renewal of the
Committee by appropriate action prior to its expiration. Members who
are not Federal employees will receive a stipend for each day they are
engaged in the performance of their duties as members of the Committee.
Members shall receive per diem and travel expenses as authorized by
section 5 U.S.C. 5703 for persons employed intermittently in Government
service. Members who are officers or employees of the United States
Government shall not receive compensation for service on the Committee.
Nominees will be invited to serve beginning from October 1, 2010.
Nominations should be typewritten. The following information should
be included in the package of material submitted for each individual
being nominated for consideration: (1) A letter of nomination that
clearly states the name and affiliation of the nominee, the basis for
the nomination (i.e., specific attributes which qualify the nominee for
service in this capacity), and a statement that the nominee is willing
to serve as a member of the Committee and appears to have no conflict
of interest that would preclude the Committee membership--potential
candidates will be asked to provide detailed information concerning
consultancies, research grants, or contracts to permit evaluation of
possible sources of conflicts of interest; (2) the nominator's name,
address, and daytime telephone number, and the home/or work address,
telephone number, and e-mail address of the individual being nominated;
and (3) a current copy of the nominee's curriculum vitae. Please submit
nominations no later than May 1, 2010.
To the extent practicable, members of the Committee should have
expertise in dealing with heritable disorders and genetic diseases that
affect the racial and ethnic and geographical diversity of newborns
served by the State newborn screening programs. The Department of
Health and Human Services will ensure that the membership of the
Committee reflects an equitable geographical and gender distribution,
provided that the effectiveness of the Committee would not be impaired.
Appointments shall be made without discrimination on the basis of age,
ethnicity, gender, sexual orientation, and cultural, religious, or
socioeconomic status.
Dated: January 11, 2010.
Mary K. Wakefield,
Administrator.
[FR Doc. 2010-671 Filed 1-14-10; 8:45 am]
BILLING CODE 4165-15-P