Agency Forms Undergoing Paperwork Reduction Act Review, 26780-26781 [2013-10853]
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Federal Register / Vol. 78, No. 89 / Wednesday, May 8, 2013 / Notices
Title: The G6 Alliance Agreement.
Parties: American President Lines,
Ltd. and APL Co. Pte, Ltd. (Operating as
one Party); Hapag-Lloyd AG; Hyundai
Merchant Marine Co., Ltd.; Mitsui
O.S.K. Lines, Ltd.; Nippon Yusen
Kaisha; and Orient Overseas Container
Line, Limited and Orient Overseas
Container Line Inc. (Operating as one
party).
Filing Party: David F. Smith, Esq.;
Cozen O’Connor; 1627 I Street NW.,
Suite 1100; Washington, DC 20006.
Synopsis: The amendment corrects
the name of Orient Overseas Container
Line Limited and Orient Overseas
Container Line Inc. (Operating as one
party).
Agreement No.: 012206.
Title: Industria Armamento
Meridionale S.P.A./K-Line Space
Charter Agreement.
Parties: Industria Armamento
Meridionale S.P.A. (‘‘Inarme’’) and
Kawasaki Kisen Kaisha, Ltd.
Filing Party: John P. Meade, Esq.;
General Counsel; K- Line America, Inc.;
6009 Bethlehem Road; Preston, MD
21655.
Synopsis: The agreement authorizes
Inarme to charter space on K-Line
vessels in the trade from the United
Kingdom to the U.S. East Coast.
Dated: May 3, 2013.
By Order of the Federal Maritime
Commission.
Karen V. Gregory,
Secretary.
FEDERAL RESERVE SYSTEM
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Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
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 will also be
available for inspection at the offices of
the Board of Governors. Interested
Jkt 229001
[FR Doc. 2013–10907 Filed 5–7–13; 8:45 am]
BILLING CODE 6210–01–P
Change in Bank Control Notices;
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies;
Correction
BILLING CODE P
17:56 May 07, 2013
Board of Governors of the Federal Reserve
System, May 3, 2013.
Margaret McCloskey Shanks,
Deputy Secretary of the Board.
FEDERAL RESERVE SYSTEM
[FR Doc. 2013–10926 Filed 5–7–13; 8:45 am]
VerDate Mar<15>2010
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.
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 June 3, 2013.
A. Federal Reserve Bank of
Minneapolis (Jacqueline G. King,
Community Affairs Officer) 90
Hennepin Avenue, Minneapolis,
Minnesota 55480–0291:
1. Lake Shore III Corporation,
Glenwood City, Wisconsin; to become a
bank holding company by acquiring 100
percent of Hiawatha National Bank,
Hager City, Wisconsin.
This notice corrects a notice (FR Doc.
78–FR 25084) published on pages
25084–25085 of the issue for Monday,
April 29, 2013.
Under the Federal Reserve Bank of
Kansas City heading, the entry for First
Central Nebraska Co, Broken Bow,
Nebraska is revised to read as follows:
A. Federal Reserve Bank of Kansas
City (Dennis Denney, Assistant Vice
President) 1 Memorial Drive, Kansas
City, Missouri 64198–0001:
1. Gene R. Giles, Alliance, Nebraska,
Sally J. Giles, Denver, Colorado, Randall
D. Giles, San Diego, California, Nicholas
G. Giles, Lincoln, Nebraska, and Lucas
G. Giles, Lincoln, Nebraska, all of the
Giles family group; the Bradley S.
Norden Irrevocable Trust and the Brett
A. Norden Irrevocable Trust, Brett A.
Norden and Bradley S. Norden, as cotrustees of both trusts, all of Highlands
Ranch, Colorado, and as members of the
Norden family group; Cheryl L. Ryan,
the Michael L. Ryan 2011 Irrevocable
Trust and the Cheryl L. Ryan 2012
Irrevocable Trust, all of Minden,
Nebraska, Jeffrey M. Ryan, Heartwell,
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Fmt 4703
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Nebraska, and Jamie Johnson, Minden,
Nebraska, as co-trustees of both trusts;
and Walter D. Wood Revocable Trust,
Walter D. Wood, trustee, both of Omaha,
Nebraska, as part of the Ryan/Wood
family group; to acquire voting shares of
First Central Nebraska Co., and thereby
indirectly acquire voting shares of
Nebraska State Bank and Trust
Company, both in Broken Bow,
Nebraska.
Comments on this application must
be received by May 23, 2012.
Board of Governors of the Federal Reserve
System, May 3, 2012.
Margaret McCloskey Shanks,
Deputy Secretary of the Board.
[FR Doc. 2013–10922 Filed 5–7–13; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day-13–0041]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC), Agency for Toxic
Substances and Disease Registry
(ATSDR) publishes a list of information
collection requests under review by the
Office of Management and Budget
(OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–7570 or send an
email to omb@cdc.gov. Send written
comments to ATSDR Desk Officer,
Office of Management and Budget,
Washington, DC 20503 or by fax to (202)
395–5806. Written comments should be
received within 30 days of this notice.
Proposed Project
National Amyotrophic Lateral
Sclerosis (ALS) Registry—Revision
(0923–0041, Expiration 7/31/13)—
Agency for Toxic Substances and
Disease Registry (ATSDR).
Background and Brief Description
On October 10, 2008, President Bush
signed S. 1382: ALS Registry Act which
amended the Public Health Service Act
to provide for the establishment of an
Amyotrophic Lateral Sclerosis (ALS)
Registry. The activities described are
part of the effort to create the National
ALS Registry. The purpose of the
registry is to: (1) Better describe the
incidence and prevalence of ALS in the
United States; (2) examine appropriate
E:\FR\FM\08MYN1.SGM
08MYN1
26781
Federal Register / Vol. 78, No. 89 / Wednesday, May 8, 2013 / Notices
factors, such as environmental and
occupational, that might be associated
with the disease; (3) better outline key
demographic factors (such as age, race
or ethnicity, gender, and family history
of individuals who are diagnosed with
the disease) associated with the disease;
and (4) better examine the connection
between ALS and other motor neuron
disorders that can be confused with
ALS, misdiagnosed as ALS, and in some
cases progress to ALS. The registry will
collect personal health information that
may provide a basis for further scientific
studies of potentially risks for
developing ALS.
After piloting methodology, on
October 18, 2010 the Agency for Toxic
Substances and Disease Registry
(ATSDR) launched the registration
component of the National ALS
Registry.
individuals with ALS which can be
combined with information obtained
from existing sources of information.
This combined data will become the
National ALS Registry and will be used
to provide more accurate estimates of
the incidence and prevalence of disease
as well as the demographic
characteristics of the cases. Information
obtained from the surveys will be used
to better characterize potential risk
factors for ALS which will lead to
further in-depth studies.
The existence of the Web site (https://
wwwn.cdc.gov/als) is being advertised
by ATSDR and advocacy groups such as
the Amyotrophic Lateral Sclerosis
Association (ALSA) and the Muscular
Dystrophy Association (MDA). There
are no costs to the respondents other
than their time. The estimated
annualized burden hours are 1,375.
The registration portion of the data
collection will be limited to information
that can be used to identify an
individual to assure that there are not
duplicate records for an individual.
Avoiding duplication of registrants due
to obtaining records from multiple
sources is imperative to get accurate
estimates of incidence and prevalence,
as well as accurate information on
demographic characteristics of the cases
of ALS.
In addition to questions required for
registration, there will be a series of
short surveys to collect information on
such things as military history,
occupations, residential history, and
family history that would not likely be
available from other sources.
This project proposes to add 10
additional risk factor surveys while
continuing to collect information on
ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondent
Form name
Person with ALS ....................
Validation questions (Screener) for suspected ALS cases ...
Registration Form of ALS cases ...........................................
Cases of ALS completing 1-time surveys .............................
Cases of ALS completing twice yearly surveys ....................
Ron A. Otten,
Director, Office of Scientific Integrity, Office
of the Associate Director for Science, Office
of the Director, Centers for Disease Control
and Prevention.
[FR Doc. 2013–10853 Filed 5–7–13; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Administration for Native Americans
Tribal Consultation; Notice of Meeting
Administration for Children
and Families, Department of Health and
Human Services.
ACTION: Notice of tribal consultation.
AGENCY:
The Department of Health and
Human Services (HHS), Administration
for Children and Families (ACF) will
host a tribal consultation to consult on
ACF programs and tribal priorities.
DATES: July 9–10, 2013.
ADDRESSES: 901 D Street SW., 7th Floor
Multipurpose Room, Washington, DC
20024.
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SUMMARY:
FOR FURTHER INFORMATION CONTACT:
Lillian A. Sparks, Commissioner,
VerDate Mar<15>2010
17:56 May 07, 2013
Jkt 229001
Number of
respondents
Administration for Native Americans at
202–401–5590, by email at
Lillian.sparks@acf.hhs.gov or by mail at
370 L’Enfant Promenade SW., 2 West,
Washington, DC 20447.
SUPPLEMENTARY INFORMATION: On
November 5, 2009, President Obama
signed the ‘‘Memorandum for the Heads
of Executive Departments and Agencies
on Tribal Consultation.’’ The President
stated that his Administration is
committed to regular and meaningful
consultation and collaboration with
tribal officials in policy decisions that
have tribal implications, including, as
an initial step, through complete and
consistent implementation of Executive
Order 13175.
The United States has a unique legal
and political relationship with Indian
tribal governments, established through
and confirmed by the Constitution of
the United States, treaties, statutes,
executive orders, and judicial decisions.
In recognition of that special
relationship, pursuant to Executive
Order 13175 of November 6, 2000,
executive departments and agencies are
charged with engaging in regular and
meaningful consultation and
collaboration with tribal officials in the
development of federal policies that
have tribal implications, and are
PO 00000
Frm 00035
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
1,670
1,500
750
750
1
1
16
2.3
Average
burden per
response
(in hours)
2/60
7/60
5/60
5/60
responsible for strengthening the
government-to-government relationship
between the United States and Indian
tribes.
HHS has taken its responsibility to
comply with Executive Order 13175
very seriously over the past decade,
including the initial implementation of
a department-wide policy on tribal
consultation and coordination in 1997,
and through multiple evaluations and
revisions of that policy, most recently in
2010. ACF has also developed its own
agency-specific consultation policy that
complements the department-wide
efforts.
ACF’s Administration for Native
Americans (ANA) will hold a tribal
consultation on the morning of July 9,
2013, to discuss the reauthorization of
ANA’s authorizing legislation, the
Native American Programs Act, and the
development of data collection elements
to collect information on the impact of
ACF funding on the members of a tribal
community.
A tribal resource day will begin the
afternoon of July 9 and the ACF Tribal
Consultation Session will begin the
morning of July 10 and continue
throughout the day until all discussions
have been completed. Other ACF
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]]>Agencies
[Federal Register Volume 78, Number 89 (Wednesday, May 8, 2013)]
[Notices]
[Pages 26780-26781]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-10853]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-13-0041]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC), Agency for
Toxic Substances and Disease Registry (ATSDR) publishes a list of
information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-7570 or send an email to
omb@cdc.gov. Send written comments to ATSDR Desk Officer, Office of
Management and Budget, Washington, DC 20503 or by fax to (202) 395-
5806. Written comments should be received within 30 days of this
notice.
Proposed Project
National Amyotrophic Lateral Sclerosis (ALS) Registry--Revision
(0923-0041, Expiration 7/31/13)--Agency for Toxic Substances and
Disease Registry (ATSDR).
Background and Brief Description
On October 10, 2008, President Bush signed S. 1382: ALS Registry
Act which amended the Public Health Service Act to provide for the
establishment of an Amyotrophic Lateral Sclerosis (ALS) Registry. The
activities described are part of the effort to create the National ALS
Registry. The purpose of the registry is to: (1) Better describe the
incidence and prevalence of ALS in the United States; (2) examine
appropriate
[[Page 26781]]
factors, such as environmental and occupational, that might be
associated with the disease; (3) better outline key demographic factors
(such as age, race or ethnicity, gender, and family history of
individuals who are diagnosed with the disease) associated with the
disease; and (4) better examine the connection between ALS and other
motor neuron disorders that can be confused with ALS, misdiagnosed as
ALS, and in some cases progress to ALS. The registry will collect
personal health information that may provide a basis for further
scientific studies of potentially risks for developing ALS.
After piloting methodology, on October 18, 2010 the Agency for
Toxic Substances and Disease Registry (ATSDR) launched the registration
component of the National ALS Registry.
The registration portion of the data collection will be limited to
information that can be used to identify an individual to assure that
there are not duplicate records for an individual. Avoiding duplication
of registrants due to obtaining records from multiple sources is
imperative to get accurate estimates of incidence and prevalence, as
well as accurate information on demographic characteristics of the
cases of ALS.
In addition to questions required for registration, there will be a
series of short surveys to collect information on such things as
military history, occupations, residential history, and family history
that would not likely be available from other sources.
This project proposes to add 10 additional risk factor surveys
while continuing to collect information on individuals with ALS which
can be combined with information obtained from existing sources of
information. This combined data will become the National ALS Registry
and will be used to provide more accurate estimates of the incidence
and prevalence of disease as well as the demographic characteristics of
the cases. Information obtained from the surveys will be used to better
characterize potential risk factors for ALS which will lead to further
in-depth studies.
The existence of the Web site (https://wwwn.cdc.gov/als) is being
advertised by ATSDR and advocacy groups such as the Amyotrophic Lateral
Sclerosis Association (ALSA) and the Muscular Dystrophy Association
(MDA). There are no costs to the respondents other than their time. The
estimated annualized burden hours are 1,375.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Person with ALS.................... Validation questions 1,670 1 2/60
(Screener) for suspected
ALS cases.
Registration Form of ALS 1,500 1 7/60
cases.
Cases of ALS completing 1- 750 16 5/60
time surveys.
Cases of ALS completing 750 2.3 5/60
twice yearly surveys.
----------------------------------------------------------------------------------------------------------------
Ron A. Otten,
Director, Office of Scientific Integrity, Office of the Associate
Director for Science, Office of the Director, Centers for Disease
Control and Prevention.
[FR Doc. 2013-10853 Filed 5-7-13; 8:45 am]
BILLING CODE 4163-18-P
