Renewal of Declaration Regarding Emergency Use of Doxycycline Hyclate Tablets Accompanied by Emergency Use Information, 61489-61490 [2010-24840]
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Federal Register / Vol. 75, No. 192 / Tuesday, October 5, 2010 / Notices
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR Part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications also will be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Additional information on all bank
holding companies may be obtained
from the National Information Center
website at www.ffiec.gov/nic/.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than October 29,
2010.
A. Federal Reserve Bank of Atlanta
(Clifford Stanford, Vice President) 1000
Peachtree Street, N.E., Atlanta, Georgia
30309:
1. PFGBI, LLC, McDonough, Georgia;
to become a bank holding company by
acquiring approximately 50.8 percent of
the outstanding voting shares of
Montgomery County Bankshares, Inc.,
and its subsidary, Montgomery County
Bank & Trust, both of Ailey, Georgia.
Board of Governors of the Federal Reserve
System, September 30, 2010.
Robert deV. Frierson,
Deputy Secretary of the Board.
[FR Doc. 2010–24901 Filed 10–4–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the Advisory Committee on
Minority Health
Office of Minority Health,
Office of the Assistant Secretary for
Health, Office of the Secretary,
Department of Health and Human
Services.
AGENCY:
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ACTION:
Notice of meeting.
As stipulated by the Federal
Advisory Committee Act, the
Department of Health and Human
Services (DHHS) is hereby giving notice
that the Advisory Committee on
Minority Health (ACMH) will hold a
meeting. This meeting is open to the
public. Preregistration is required for
both public attendance and comment.
Any individual who wishes to attend
the meeting and/or participate in the
public comment session should e-mail
acmh@osophs.dhhs.gov.
DATES: The meeting will be held on
Monday, November 15, 2010 from 9
a.m. to 5 p.m. and Tuesday, November
16, 2010 from 9 a.m. to 1 p.m.
ADDRESSES: The meeting will be held at
the Doubletree Hotel, 1515 Rhode Island
Ave., NW., Washington, DC 20005.
FOR FURTHER INFORMATION CONTACT: Ms.
Monica A. Baltimore, Tower Building,
1101 Wootton Parkway, Suite 600,
Rockville, Maryland 20852. Phone: 240–
453–2882, Fax: 240–453–2883.
SUPPLEMENTARY INFORMATION: In
accordance with Public Law 105–392,
the ACMH was established to provide
advice to the Deputy Assistant Secretary
for Minority Health in improving the
health of each racial and ethnic
minority group and on the development
of goals and specific program activities
of the Office of Minority Health.
Topics to be discussed during this
meeting will include increasing the
health care workforce and strategies to
improve the health of racial and ethnic
minority populations through the
development of health policies and
programs that will help eliminate health
disparities, as well as other related
issues.
Public attendance at the meeting is
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
designated contact person at least
fourteen (14) business days prior to the
meeting. Members of the public will
have an opportunity to provide
comments at the meeting. Public
comments will be limited to three
minutes per speaker. Individuals who
would like to submit written statements
should mail or fax their comments to
the Office of Minority Health at least
seven (7) business days prior to the
meeting. Any members of the public
who wish to have printed material
distributed to ACMH committee
members should submit their materials
to the Executive Secretary, ACMH,
Tower Building, 1101 Wootton
SUMMARY:
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61489
Parkway, Suite 600, Rockville,
Maryland 20852, prior to close of
business November 5, 2010.
Dated: September 23, 2010.
Garth N. Graham,
Deputy Assistant Secretary for Minority
Health, Office of Minority Health, Office of
the Assistant Secretary for Health, Office of
the Secretary, U.S. Department of Health and
Human Services.
[FR Doc. 2010–24880 Filed 10–4–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Renewal of Declaration Regarding
Emergency Use of Doxycycline Hyclate
Tablets Accompanied by Emergency
Use Information
AGENCY:
Office of the Secretary (OS),
HHS.
ACTION:
Notice.
The Secretary of Homeland
Security determined on September 23,
2008 that there is a significant potential
for a domestic emergency involving a
heightened risk of attack with a
specified biological, chemical,
radiological, or nuclear agent or
agents—in this case, Bacillus anthracis.
On the basis of this determination, the
Secretary of Health and Human Services
is renewing the October 1, 2008
declaration by former Secretary Michael
O. Leavitt of an emergency justifying the
authorization of emergency use of
doxycycline hyclate tablets
accompanied by emergency use
information subject to the terms of any
authorization issued by the Food and
Drug Commissioner under 21 U.S.C.
360bbb–3(a). This notice is being issued
in accordance with section 564(b)(4) of
the Federal Food, Drug, and Cosmetic
Act, 21 U.S.C. 360bbb–3(b)(4).
DATES: This Notice and referenced HHS
declaration are effective as of October 1,
2010.
FOR FURTHER INFORMATION CONTACT:
Nicole Lurie, MD MSPH, Assistant
Secretary for Preparedness and
Response, Office of the Secretary,
Department of Health and Human
Services, 200 Independence Avenue,
SW., Washington, DC 20201, Telephone
(202) 205–2882 (this is not a toll free
number).
SUPPLEMENTARY INFORMATION: On
September 23, 2008, former Secretary of
Homeland Security, Michael Chertoff,
determined that there is a significant
potential for a domestic emergency,
involving a heightened risk of attack
SUMMARY:
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Federal Register / Vol. 75, No. 192 / Tuesday, October 5, 2010 / Notices
with a specified biological, chemical,
radiological, or nuclear agent or
agents—in this case, Bacillus anthracis,
although there is no current domestic
emergency involving anthrax, no
current heightened risk of an anthrax
attack, and no credible information
indicating an imminent threat of an
attack involving Bacillus anthracis.
Pursuant to section 564(b) of the Federal
Food, Drug and Cosmetic Act, 21 U.S.C.
360bbb–3(b), and on the basis of such
determination, on October 1, 2008,
former Secretary of Health and Human
Services, Michael O. Leavitt, declared
an emergency justifying the
authorization of the emergency use of
doxycycline hyclate tablets
accompanied by emergency use
information subject to the terms of any
authorization issued under 21 U.S.C.
360bbb–3(a).1 Pursuant to section
564(b)(2)(B) of the Federal Food, Drug
and Cosmetic Act, 21 U.S.C. 360bbb–
3(b), and on the basis of Secretary
Chertoff’s September 23, 2008
determination, I hereby renew former
Secretary Leavitt’s October 1, 2008
declaration of an emergency, which I
previously renewed on October 1, 2009,
justifying the authorization of the
emergency use of doxycycline hyclate
tablets accompanied by emergency use
information subject to the terms of any
authorization issued under 21 U.S.C.
360bbb–3(a). I am issuing this notice in
accordance with section 564(b)(4) of the
Federal Food, Drug, and Cosmetic Act,
21 U.S.C. 360bbb–3(b)(4).
Dated: September 24, 2010.
Kathleen Sebelius,
Secretary.
[FR Doc. 2010–24840 Filed 9–30–10; 11:15 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
OMB No.: 0970–0175.
Description: Section 466(a)(5)(C) of
the Social Security Act requires States
to pass laws ensuring a simple civil
process for voluntarily acknowledging
paternity under which the State must
provide that the mother and putative
father must be given notice, orally and
in writing, of the benefits and legal
responsibilities and consequences of
acknowledging paternity. The
information is to be used by hospitals,
birth record agencies, and other entities
participating in the voluntary paternity
establishment program that collect
information from the parents of children
that are born out of wedlock.
Respondents: The parents of children
that are born out of wedlock.
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: Voluntary Establishment of
Paternity—NPRM.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
1,167,097
1
0.17
198,406.49
Estimated Total Annual Burden Hours: ....................................................
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None .................................................................................................................
........................
........................
........................
198,406.49
In compliance with the requirements
of Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded 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. E-mail address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.
The Department specifically requests
comments on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
1 Pursuant to section 564(b)(4) of the FFDCA,
notice of the determination by the Secretary, DHS,
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18:36 Oct 04, 2010
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agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: September 30, 2010.
Robert Sargis,
Reports Clearance Officer.
AGENCY:
[FR Doc. 2010–24893 Filed 10–4–10; 8:45 am]
SUMMARY:
Food and Drug Administration
[Docket No. FDA–2010–N–0502]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; National Consumer
Surveys on Understanding the Risks
and Benefits of FDA-Regulated Medical
Products
Food and Drug Administration,
HHS.
ACTION:
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Notice.
The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information and to allow 60 days for
and the declaration by the Secretary, HHS, was
provided at 73 FR 58242 (October 6, 2008).
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Agencies
[Federal Register Volume 75, Number 192 (Tuesday, October 5, 2010)]
[Notices]
[Pages 61489-61490]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-24840]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
Renewal of Declaration Regarding Emergency Use of Doxycycline
Hyclate Tablets Accompanied by Emergency Use Information
AGENCY: Office of the Secretary (OS), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Secretary of Homeland Security determined on September 23,
2008 that there is a significant potential for a domestic emergency
involving a heightened risk of attack with a specified biological,
chemical, radiological, or nuclear agent or agents--in this case,
Bacillus anthracis. On the basis of this determination, the Secretary
of Health and Human Services is renewing the October 1, 2008
declaration by former Secretary Michael O. Leavitt of an emergency
justifying the authorization of emergency use of doxycycline hyclate
tablets accompanied by emergency use information subject to the terms
of any authorization issued by the Food and Drug Commissioner under 21
U.S.C. 360bbb-3(a). This notice is being issued in accordance with
section 564(b)(4) of the Federal Food, Drug, and Cosmetic Act, 21
U.S.C. 360bbb-3(b)(4).
DATES: This Notice and referenced HHS declaration are effective as of
October 1, 2010.
FOR FURTHER INFORMATION CONTACT: Nicole Lurie, MD MSPH, Assistant
Secretary for Preparedness and Response, Office of the Secretary,
Department of Health and Human Services, 200 Independence Avenue, SW.,
Washington, DC 20201, Telephone (202) 205-2882 (this is not a toll free
number).
SUPPLEMENTARY INFORMATION: On September 23, 2008, former Secretary of
Homeland Security, Michael Chertoff, determined that there is a
significant potential for a domestic emergency, involving a heightened
risk of attack
[[Page 61490]]
with a specified biological, chemical, radiological, or nuclear agent
or agents--in this case, Bacillus anthracis, although there is no
current domestic emergency involving anthrax, no current heightened
risk of an anthrax attack, and no credible information indicating an
imminent threat of an attack involving Bacillus anthracis. Pursuant to
section 564(b) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C.
360bbb-3(b), and on the basis of such determination, on October 1,
2008, former Secretary of Health and Human Services, Michael O.
Leavitt, declared an emergency justifying the authorization of the
emergency use of doxycycline hyclate tablets accompanied by emergency
use information subject to the terms of any authorization issued under
21 U.S.C. 360bbb-3(a).\1\ Pursuant to section 564(b)(2)(B) of the
Federal Food, Drug and Cosmetic Act, 21 U.S.C. 360bbb-3(b), and on the
basis of Secretary Chertoff's September 23, 2008 determination, I
hereby renew former Secretary Leavitt's October 1, 2008 declaration of
an emergency, which I previously renewed on October 1, 2009, justifying
the authorization of the emergency use of doxycycline hyclate tablets
accompanied by emergency use information subject to the terms of any
authorization issued under 21 U.S.C. 360bbb-3(a). I am issuing this
notice in accordance with section 564(b)(4) of the Federal Food, Drug,
and Cosmetic Act, 21 U.S.C. 360bbb-3(b)(4).
---------------------------------------------------------------------------
\1\ Pursuant to section 564(b)(4) of the FFDCA, notice of the
determination by the Secretary, DHS, and the declaration by the
Secretary, HHS, was provided at 73 FR 58242 (October 6, 2008).
Dated: September 24, 2010.
Kathleen Sebelius,
Secretary.
[FR Doc. 2010-24840 Filed 9-30-10; 11:15 am]
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