Agency Information Collection Activities; Proposed Collection; Public Comment Request, 66360-66361 [2013-26401]
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66360
Federal Register / Vol. 78, No. 214 / Tuesday, November 5, 2013 / Notices
Dated: October 31, 2013.
Robert E. Feldman,
Committee Management Officer, Federal
Deposit Insurance Corporation.
[FR Doc. 2013–26439 Filed 11–4–13; 8:45 am]
BILLING CODE 6714–01–P
FEDERAL ELECTION COMMISSION
Sunshine Act Meeting
Federal Election Commission.
Thursday, November 7,
2013 at 10:00 a.m.
PLACE: 999 E Street NW., Washington,
DC.
STATUS: This meeting will be closed to
the public.
ITEMS TO BE DISCUSSED: Compliance
matters pursuant to 2 U.S.C. 437g.
Matters concerning participation in civil
actions or proceedings or arbitration.
Internal personnel rules and procedures
or matters affecting a particular
employee.
*
*
*
*
*
PERSON TO CONTACT FOR INFORMATION:
Judith Ingram, Press Officer, Telephone:
(202) 694–1220.
AGENCY:
DATE AND TIME:
Shawn Woodhead Werth,
Secretary of the Commission.
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 December 2,
2013.
A. Federal Reserve Bank of Kansas
City (Dennis Denney, Assistant Vice
President) 1 Memorial Drive, Kansas
City, Missouri 64198–0001:
1. Geneva State Company, Geneva,
Nebraska; to acquire 100 percent of the
voting shares of, and merge with
Riverdale Bancshares, Inc., and thereby
indirectly acquire voting shares of State
Bank of Riverdale, both in Riverdale,
Nebraska.
Board of Governors of the Federal Reserve
System, October 31, 2013.
Michael J. Lewandowski,
Associate Secretary of the Board.
[FR Doc. 2013–26440 Filed 11–4–13; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2013–26551 Filed 11–1–13; 11:15 am]
Office of the Secretary
BILLING CODE 6715–01–P
[Document Identifier HHS–OS–20790–60D]
FEDERAL RESERVE SYSTEM
Agency Information Collection
Activities; Proposed Collection; Public
Comment Request
wreier-aviles on DSK5TPTVN1PROD with NOTICES
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
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
VerDate Mar<15>2010
15:22 Nov 04, 2013
Jkt 232001
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
In compliance with section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, announces plans
to submit a new Information Collection
Request (ICR), described below, to the
Office of Management and Budget
(OMB). Prior to submitting that ICR to
OMB, OS seeks comments from the
public regarding the burden estimate,
below, or any other aspect of the ICR.
DATES: Comments on the ICR must be
received on or before January 6, 2014.
ADDRESSES: Submit your comments to
Information.CollectionClearance@
hhs.gov or by calling (202) 690–6162.
FOR FURTHER INFORMATION CONTACT:
Information Collection Clearance staff,
Information.CollectionClearance@
hhs.gov or (202) 690–6162.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
SUMMARY:
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
information, please include the
document identifier HHS–OS–20790–
60D for reference. Information
Collection Request Title: Title X Family
Planning Outreach and Enrollment Data
Collection Form.
Abstract: The Office of Population
Affairs within the Office of the Assistant
Secretary for Health seeks to collect data
from the Title X service delivery
grantees on efforts related to outreach
and enrollment to assist individuals in
obtaining health insurance available as
a result of the Affordable Care Act
(ACA). Grantees will be asked to collect
and report information on the numbers
of individuals who are; (1) Assisted by
a trained health center worker; (2)
number of individuals who receive an
eligibility determination for the
marketplace, Medicaid or CHIP with the
assistance of a trained worker; and (3)
number of individuals who enroll in an
insurance program with the assistance
of a trained worker. The information
will be reported for all sites in their
grantee network.
Need and Proposed Use of the
Information:
The Title X Family Planning Program
(‘‘Title X program’’ or ‘‘program’’) is the
only Federal grant program dedicated
solely to providing individuals with
comprehensive family planning and
related preventive health services (e.g.,
screening for breast and cervical cancer,
sexually transmitted diseases (STDs),
and human immunodeficiency virus
[HIV]). By law, priority is given to
persons from low-income families
(Section 1006[c] of Title X of the Public
Health Service Act, 42 USC 300). The
Office of Population Affairs (OPA)
within the Office of the Assistant
Secretary for Health administers the
Title X program.
In fiscal year 2013, Congress
appropriated approximately $296.8
million for Title X family planning
activities. In accordance with the statute
and regulations (42 Code of Federal
Regulations [CFR] Part 59), at least 90%
of the appropriation is used for clinical
family planning services. In 2012, 98
Title X grantees provided family
planning services to five million women
and men through a network of 4,400
community-based clinics that include
state and local health departments,
tribal organizations, and other public
and private nonprofit agencies. There is
at least one clinic that receives Title X
funds and provides services as required
under the Title X statute in 73% of U.S.
counties.
Sixty percent of the clients seen at
Title X funded service sites self-identify
as being uninsured. Seventy percent of
the total clients are under the age 30.
E:\FR\FM\05NON1.SGM
05NON1
Federal Register / Vol. 78, No. 214 / Tuesday, November 5, 2013 / Notices
Thus Title X service sites see a large
proportion of young and uninsured
individuals. Over the past years, OPA
has encouraged grantees to develop
enrollment programs to ensure that
clients who are currently uninsured
understand new health insurance
options that are available as a result of
the ACA. Some sites already assist
individuals with enrolling in Medicaid
and other public insurance programs.
With the availability of the health
insurance marketplace, many more
service delivery sites are assisting
clients enroll in health insurance
programs.
OPA does not have any data on how
many sites are assisting and enrolling
clients into health insurance programs.
Thus we seek to collect this data in
order to understand the impact of Title
X funded service sites on assisting and
enrolling clients into insurance
programs. We will utilize this
information to guide strategic planning
around how Title X service sites and
prepare for, and assist with, the full
implementation of the ACA. Through a
separate data collection process called
the Family Planning Annual Report
(FPAR) (OMB No. 0990–0221,
expiration January 31, 2016), OPA
collects information on the insurance
status of the clients served. With the
implementation of the ACA, many of
the traditional clients served by Title X
service sites will qualify for health
insurance. Due to the varying resources
available at the State level to conduct
outreach and enrollment, OPA has
authorized grantees to use funding to
conduct outreach and enrollment
activities. However, we are not currently
collecting data on how many sites are
conducting such activities, the impact of
those activities in enrolling clients into
health insurance programs, and the
need for additional resources to conduct
outreach and enrollment. By collecting
information on how many clients are
assisted and enrolled in health
insurance programs, OPA can; (1)
measure the impact of Title X service
sites in enrolling clients into insurance
programs; (2) design strategic initiatives
to encourage outreach and enrollment;
and (3) better understand the impact of
the Affordable Care Act on Title X
service delivery sites.
Likely Respondents: This annual
reporting requirement is for family
planning services delivery projects
authorized and funded by the Title X
Family Planning Program [‘‘Population
Research and Voluntary Family
Planning Programs’’ (Pub. L. 91–572)],
66361
which was enacted in 1970 as Title X of
the Public Health Service Act (Section
1001 of Title X of the Public Health
Service Act, 42 United States Code
[USC] 300).
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose or provide the information
requested. This includes the time
needed to review instructions, to
develop, acquire, install and utilize
technology and systems for the purpose
of collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information, to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information, and to
transmit or otherwise disclose the
information.
This data is currently being collected
by the Health Resources and Services
Administration (HRSA) and the burden
estimate is based on the supporting
statement from their OMB application.
The total annual burden hours
estimated for this ICR are summarized
in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Form name
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
hours
Outreach and Enrollment Activities .................................................................
95
1
1
95
OS specifically requests comments on
(1) the necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions, (2) the accuracy of the
estimated burden, (3) ways to enhance
the quality, utility, and clarity of the
information to be collected, and (4) the
use of automated collection techniques
or other forms of information
technology to minimize the information
collection burden.
wreier-aviles on DSK5TPTVN1PROD with NOTICES
Darius Taylor,
Deputy, Information Collection Clearance
Officer.
[FR Doc. 2013–26401 Filed 11–4–13; 8:45 am]
BILLING CODE 4150–47–P
VerDate Mar<15>2010
15:22 Nov 04, 2013
Jkt 232001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60-Day–14–14BE]
Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–7570 or send
comments to CDC/ATSDR LeRoy
Richardson, 1600 Clifton Road, MS D–
PO 00000
Frm 00033
Fmt 4703
Sfmt 4703
74, Atlanta, GA 30333 or send an email
to omb@cdc.gov.
Comments are invited 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
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance 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. Written comments should
be received within 60 days of this
notice.
Proposed Project
CDC Worksite Health Scorecard—
New—National Center for Chronic
Disease Prevention and Health
E:\FR\FM\05NON1.SGM
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]]>Agencies
[Federal Register Volume 78, Number 214 (Tuesday, November 5, 2013)]
[Notices]
[Pages 66360-66361]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-26401]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
[Document Identifier HHS-OS-20790-60D]
Agency Information Collection Activities; Proposed Collection;
Public Comment Request
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the Secretary (OS), Department of
Health and Human Services, announces plans to submit a new Information
Collection Request (ICR), described below, to the Office of Management
and Budget (OMB). Prior to submitting that ICR to OMB, OS seeks
comments from the public regarding the burden estimate, below, or any
other aspect of the ICR.
DATES: Comments on the ICR must be received on or before January 6,
2014.
ADDRESSES: Submit your comments to
Information.CollectionClearance@hhs.gov or by calling (202) 690-6162.
FOR FURTHER INFORMATION CONTACT: Information Collection Clearance
staff, Information.CollectionClearance@hhs.gov or (202) 690-6162.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the document identifier HHS-OS-20790-60D
for reference. Information Collection Request Title: Title X Family
Planning Outreach and Enrollment Data Collection Form.
Abstract: The Office of Population Affairs within the Office of the
Assistant Secretary for Health seeks to collect data from the Title X
service delivery grantees on efforts related to outreach and enrollment
to assist individuals in obtaining health insurance available as a
result of the Affordable Care Act (ACA). Grantees will be asked to
collect and report information on the numbers of individuals who are;
(1) Assisted by a trained health center worker; (2) number of
individuals who receive an eligibility determination for the
marketplace, Medicaid or CHIP with the assistance of a trained worker;
and (3) number of individuals who enroll in an insurance program with
the assistance of a trained worker. The information will be reported
for all sites in their grantee network.
Need and Proposed Use of the Information:
The Title X Family Planning Program (``Title X program'' or
``program'') is the only Federal grant program dedicated solely to
providing individuals with comprehensive family planning and related
preventive health services (e.g., screening for breast and cervical
cancer, sexually transmitted diseases (STDs), and human
immunodeficiency virus [HIV]). By law, priority is given to persons
from low-income families (Section 1006[c] of Title X of the Public
Health Service Act, 42 USC 300). The Office of Population Affairs (OPA)
within the Office of the Assistant Secretary for Health administers the
Title X program.
In fiscal year 2013, Congress appropriated approximately $296.8
million for Title X family planning activities. In accordance with the
statute and regulations (42 Code of Federal Regulations [CFR] Part 59),
at least 90% of the appropriation is used for clinical family planning
services. In 2012, 98 Title X grantees provided family planning
services to five million women and men through a network of 4,400
community-based clinics that include state and local health
departments, tribal organizations, and other public and private
nonprofit agencies. There is at least one clinic that receives Title X
funds and provides services as required under the Title X statute in
73% of U.S. counties.
Sixty percent of the clients seen at Title X funded service sites
self-identify as being uninsured. Seventy percent of the total clients
are under the age 30.
[[Page 66361]]
Thus Title X service sites see a large proportion of young and
uninsured individuals. Over the past years, OPA has encouraged grantees
to develop enrollment programs to ensure that clients who are currently
uninsured understand new health insurance options that are available as
a result of the ACA. Some sites already assist individuals with
enrolling in Medicaid and other public insurance programs. With the
availability of the health insurance marketplace, many more service
delivery sites are assisting clients enroll in health insurance
programs.
OPA does not have any data on how many sites are assisting and
enrolling clients into health insurance programs. Thus we seek to
collect this data in order to understand the impact of Title X funded
service sites on assisting and enrolling clients into insurance
programs. We will utilize this information to guide strategic planning
around how Title X service sites and prepare for, and assist with, the
full implementation of the ACA. Through a separate data collection
process called the Family Planning Annual Report (FPAR) (OMB No. 0990-
0221, expiration January 31, 2016), OPA collects information on the
insurance status of the clients served. With the implementation of the
ACA, many of the traditional clients served by Title X service sites
will qualify for health insurance. Due to the varying resources
available at the State level to conduct outreach and enrollment, OPA
has authorized grantees to use funding to conduct outreach and
enrollment activities. However, we are not currently collecting data on
how many sites are conducting such activities, the impact of those
activities in enrolling clients into health insurance programs, and the
need for additional resources to conduct outreach and enrollment. By
collecting information on how many clients are assisted and enrolled in
health insurance programs, OPA can; (1) measure the impact of Title X
service sites in enrolling clients into insurance programs; (2) design
strategic initiatives to encourage outreach and enrollment; and (3)
better understand the impact of the Affordable Care Act on Title X
service delivery sites.
Likely Respondents: This annual reporting requirement is for family
planning services delivery projects authorized and funded by the Title
X Family Planning Program [``Population Research and Voluntary Family
Planning Programs'' (Pub. L. 91-572)], which was enacted in 1970 as
Title X of the Public Health Service Act (Section 1001 of Title X of
the Public Health Service Act, 42 United States Code [USC] 300).
Burden Statement: Burden in this context means the time expended by
persons to generate, maintain, retain, disclose or provide the
information requested. This includes the time needed to review
instructions, to develop, acquire, install and utilize technology and
systems for the purpose of collecting, validating and verifying
information, processing and maintaining information, and disclosing and
providing information, to train personnel and to be able to respond to
a collection of information, to search data sources, to complete and
review the collection of information, and to transmit or otherwise
disclose the information.
This data is currently being collected by the Health Resources and
Services Administration (HRSA) and the burden estimate is based on the
supporting statement from their OMB application.
The total annual burden hours estimated for this ICR are summarized
in the table below.
Total Estimated Annualized Burden--Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Form name Number of responses per per response Total burden
respondents respondent (in hours) hours
----------------------------------------------------------------------------------------------------------------
Outreach and Enrollment Activities.......... 95 1 1 95
----------------------------------------------------------------------------------------------------------------
OS specifically requests comments on (1) the necessity and utility
of the proposed information collection for the proper performance of
the agency's functions, (2) the accuracy of the estimated burden, (3)
ways to enhance the quality, utility, and clarity of the information to
be collected, and (4) the use of automated collection techniques or
other forms of information technology to minimize the information
collection burden.
Darius Taylor,
Deputy, Information Collection Clearance Officer.
[FR Doc. 2013-26401 Filed 11-4-13; 8:45 am]
BILLING CODE 4150-47-P
