Agency Information Collection Activities: Submission for OMB Review; Comment Request, 12545-12546 [2010-5673]
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Federal Register / Vol. 75, No. 50 / Tuesday, March 16, 2010 / Notices
President) 701 East Byrd Street,
Richmond, Virginia 23261–4528:≤
1. Peden B. McLeod, Mary H. McLeod,
John R. McLeod, all of Walterboro,
South Carolina; Peden B. McLeod, Jr.,
Mt. Pleasant, South Carolina; Mary C.
Benson, Columbia, South Carolina; and
Rhoda L. Perry, Hendersonville, North
Carolina; acting in concert to retain
voting shares of Communitycorp, and
thereby indirectly retain voting shares of
Bank of Walterboro, both of Walterboro,
South Carolina.
B. Federal Reserve Bank of St. Louis
(Glenda Wilson, Community Affairs
Officer) P.O. Box 442, St. Louis,
Missouri 63166–2034:
1. First State Bancorp, Inc. Employee
Stock Ownership Plan (Irvin G. Waller
and Duane S. Michie as trustees), all of
Caruthersville, Missouri; to acquire
voting shares of First State Bancorp,
Inc., and thereby indirectly acquire
voting shares of First State Bank and
Trust Company, both of Caruthersville,
Missouri.
Board of Governors of the Federal Reserve
System, March 11, 2010.
Jennifer J. Johnson,
Secretary of the Board.
[FR Doc. 2010–5686 Filed 3–15–10; 8:45 am]
BILLING CODE 6210–01–S
Board of Governors of the Federal Reserve
System, March 11, 2010.
Jennifer J. Johnson,
Secretary of the Board.
FEDERAL RESERVE SYSTEM
sroberts on DSKD5P82C1PROD 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 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
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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 April 9, 2010.
A. Federal Reserve Bank of
Philadelphia (Michael E. Collins, Senior
Vice President) 100 North 6th Street,
Philadelphia, Pennsylvania 19105–
1521:
1. Tower Bancorp, Inc., Harrisburg,
Pennsylvania; to merge with First
Chester County Corporation, and
thereby indirectly acquire First National
Bank of Chester County, both of West
Chester, Pennsylvania.
B. Federal Reserve Bank of St. Louis
(Glenda Wilson, Community Affairs
Officer) P.O. Box 442, St. Louis,
Missouri 63166–2034:
1. Du Quoin State Bank ESOP, Du
Quoin, Illinois; to become a bank
holding company by retaining voting
shares of Perry County Bancorp, Inc.,
and Du Quoin State Bank, both of Du
Quoin, Illinois.
[FR Doc. 2010–5687 Filed 3–15–10; 8:45 am]
BILLING CODE 6210–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Periodically, the Health Resources
and Services Administration (HRSA)
publishes abstracts of information
requests under review by the Office of
Management and Budget (OMB), in
compliance with the Paperwork
Reduction Act of 1995 (44 U.S.C.
Chapter 35). To request a copy of the
clearance requests submitted to OMB for
review, e-mail paperwork@hrsa.gov or
call the HRSA Reports Clearance Officer
at (301) 443–1129.
The following request has been
submitted to the Office of Management
and Budget for review under the
Paperwork Reduction Act of 1995:
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12545
Proposed Project: Ryan White
Treatment and Modernization Act Part
A Minority AIDS Initiative Report (the
Part A MAI Report). (OMB No. 0915–
0304): Extension
HRSA’s HIV/AIDS Bureau (HAB)
administers Part A of Title XXVI of the
Public Health Service Act as amended
by Congress in October 2009 (Ryan
White HIV/AIDS Treatment Extension
Act of 2009). Part A provides emergency
relief for areas with substantial need for
HIV/AIDS care and support services that
are most severely affected by the HIV/
AIDS epidemic, including eligible
metropolitan areas (EMA) and
Transitional Grant Areas (TGAs). As a
component of Part A (previously Title I),
the purpose of the Minority AIDS
Initiative (MAI) Supplement is to
improve access to high quality HIV care
services and health outcomes for
individuals in disproportionately
impacted communities of color who are
living with HIV disease, including
African-Americans, Latinos, Native
Americans, Asian Americans, Native
Hawaiians and Pacific Islanders
(Section 2693(b)(2)(A) of the Public
Health Service (PHS) Act). Since the
purpose of the Part A MAI is to expand
access to medical, health, and social
support services for disproportionately
impacted racial/ethnic minority
populations living with HIV/AIDS, who
are not yet in care, it is important that
HRSA is able to report on minorities
served by the Part A MAI.
The Part A MAI Report is a data
collection instrument in which grantees
report on the number and characteristics
of clients served and services provided.
The Part A MAI Report, first approved
for use in March 2006, is designed to
collect performance data from Part A
Grantees that will not change, and it has
two parts: (1) a web-based data entry
application that collects standardized
quantitative and qualitative information,
and (2) an accompanying narrative
report. Grantees submit two Part A MAI
Reports annually: Part A MAI Plan
(Plan) and the Part A MAI Year-End
Annual Report (Annual Report). The
Plan and Annual Report components of
the report are linked to minimize the
reporting burden, and include dropdown menu responses, fields for
reporting budget, expenditure and
aggregated client level data, and openended responses for describing client or
service-level outcomes. Together the
Plan and Annual Report components
collect information from grantees on
MAI-funded services, expenditure
patterns, the number and demographics
of clients served, and client-level
outcomes.
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12546
Federal Register / Vol. 75, No. 50 / Tuesday, March 16, 2010 / Notices
The MAI Plan Narrative that
accompanies the Plan Web forms
provides (1) an explanation of the data
submitted in the Plan Web forms; (2) a
summary of the Plan, including the plan
and timeline for disbursing funds,
monitoring service delivery, and
implementing any service-related
capacity development or technical
assistance activities; and (3) the plan
and timeline for documenting clientlevel outcome measures. In addition, if
the EMA/TGA revised any planned
services, allocation amounts or target
communities after their grant
application was submitted, the changes
must be highlighted and explained. The
accompanying MAI Annual Report
Narrative describes (1) progress towards
achieving specific goals and objectives
identified in the Grantee’s approved
MAI Plan for that fiscal year and in
linking MAI services/activities to Part A
and other Ryan White HIV/AIDS
Program services; (2) achievements in
relation to client-level health outcomes;
(3) summary of challenges or barriers at
the provider or grantee levels, the
strategies and/or action steps
implemented to address them, and
lessons learned; and, (4) discussion of
MAI technical assistance needs
identified by the EMA/TGA.
This information is needed to monitor
and assess: (1) Changes in the type and
amount of HIV/AIDS health care and
related services being provided to each
disproportionately impacted community
of color; (2) the aggregate number of
persons receiving HIV/AIDS services
within each racial and ethnic
community; and (3) the impact of Part
A MAI-funded services in terms of
client-level and service-level health
outcomes. The information also is used
to plan new technical assistance and
capacity development activities, and
inform the HRSA policy and program
management functions. The data
provided to HRSA does not contain
individual or personally identifiable
information.
The annual estimated response
burden for grantees is as follows:
Form
Estimated
number of
respondents
Responses
per
respondent
Total
responses
Hours per
response
Total burden
hours
Part A MAI Report ...............................................................
56
2
112
5
560
Note: Data collection system enhancements have resulted in a shortened response burden (from 6 to 5 total hours per response) for respondents since the previous OMB approval request.
E-mail comments to
paperwork@hrsa.gov or mail the HRSA
Reports Clearance Officer, Room 10–33,
Parklawn Building, 5600 Fishers Lane,
Rockville, Maryland 20857. Written
comments should be received within 30
days of this notice.
Dated: March 5, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information
Coordination.
[FR Doc. 2010–5673 Filed 3–15–10; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0120]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Cosmetic Labeling
Regulations
AGENCY:
Food and Drug Administration,
sroberts on DSKD5P82C1PROD with NOTICES
Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined in
44 U.S.C. 3502(3) and 5 CFR 1320.3(c)
and includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires Federal agencies
SUPPLEMENTARY INFORMATION:
HHS.
ACTION:
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
information collection provisions in
FDA’s cosmetic labeling regulations.
DATES: Submit written or electronic
comments on the collection of
information by May 17, 2010.
ADDRESSES: Submit electronic
comments on the collection of
information to https://
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Denver Presley, Jr., Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
3793.
Notice.
SUMMARY: 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, including each proposed
extension of an existing collection of
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to provide a 60-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
Cosmetic Labeling Regulations—21 CFR
Part 701 (OMB Control Number 0910–
0599)—Extension
The Federal Food, Drug, and Cosmetic
Act (the act) and the Fair Packaging and
Labeling Act (the FPLA) require that
cosmetic manufacturers, packers, and
distributors disclose information about
themselves or their products on the
labels or labeling of their products.
E:\FR\FM\16MRN1.SGM
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]]>Agencies
[Federal Register Volume 75, Number 50 (Tuesday, March 16, 2010)]
[Notices]
[Pages 12545-12546]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-5673]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
Periodically, the Health Resources and Services Administration
(HRSA) publishes abstracts of information requests under review by the
Office of Management and Budget (OMB), in compliance with the Paperwork
Reduction Act of 1995 (44 U.S.C. Chapter 35). To request a copy of the
clearance requests submitted to OMB for review, e-mail
paperwork@hrsa.gov or call the HRSA Reports Clearance Officer at (301)
443-1129.
The following request has been submitted to the Office of
Management and Budget for review under the Paperwork Reduction Act of
1995:
Proposed Project: Ryan White Treatment and Modernization Act Part A
Minority AIDS Initiative Report (the Part A MAI Report). (OMB No. 0915-
0304): Extension
HRSA's HIV/AIDS Bureau (HAB) administers Part A of Title XXVI of
the Public Health Service Act as amended by Congress in October 2009
(Ryan White HIV/AIDS Treatment Extension Act of 2009). Part A provides
emergency relief for areas with substantial need for HIV/AIDS care and
support services that are most severely affected by the HIV/AIDS
epidemic, including eligible metropolitan areas (EMA) and Transitional
Grant Areas (TGAs). As a component of Part A (previously Title I), the
purpose of the Minority AIDS Initiative (MAI) Supplement is to improve
access to high quality HIV care services and health outcomes for
individuals in disproportionately impacted communities of color who are
living with HIV disease, including African-Americans, Latinos, Native
Americans, Asian Americans, Native Hawaiians and Pacific Islanders
(Section 2693(b)(2)(A) of the Public Health Service (PHS) Act). Since
the purpose of the Part A MAI is to expand access to medical, health,
and social support services for disproportionately impacted racial/
ethnic minority populations living with HIV/AIDS, who are not yet in
care, it is important that HRSA is able to report on minorities served
by the Part A MAI.
The Part A MAI Report is a data collection instrument in which
grantees report on the number and characteristics of clients served and
services provided. The Part A MAI Report, first approved for use in
March 2006, is designed to collect performance data from Part A
Grantees that will not change, and it has two parts: (1) a web-based
data entry application that collects standardized quantitative and
qualitative information, and (2) an accompanying narrative report.
Grantees submit two Part A MAI Reports annually: Part A MAI Plan (Plan)
and the Part A MAI Year-End Annual Report (Annual Report). The Plan and
Annual Report components of the report are linked to minimize the
reporting burden, and include drop-down menu responses, fields for
reporting budget, expenditure and aggregated client level data, and
open-ended responses for describing client or service-level outcomes.
Together the Plan and Annual Report components collect information from
grantees on MAI-funded services, expenditure patterns, the number and
demographics of clients served, and client-level outcomes.
[[Page 12546]]
The MAI Plan Narrative that accompanies the Plan Web forms provides
(1) an explanation of the data submitted in the Plan Web forms; (2) a
summary of the Plan, including the plan and timeline for disbursing
funds, monitoring service delivery, and implementing any service-
related capacity development or technical assistance activities; and
(3) the plan and timeline for documenting client-level outcome
measures. In addition, if the EMA/TGA revised any planned services,
allocation amounts or target communities after their grant application
was submitted, the changes must be highlighted and explained. The
accompanying MAI Annual Report Narrative describes (1) progress towards
achieving specific goals and objectives identified in the Grantee's
approved MAI Plan for that fiscal year and in linking MAI services/
activities to Part A and other Ryan White HIV/AIDS Program services;
(2) achievements in relation to client-level health outcomes; (3)
summary of challenges or barriers at the provider or grantee levels,
the strategies and/or action steps implemented to address them, and
lessons learned; and, (4) discussion of MAI technical assistance needs
identified by the EMA/TGA.
This information is needed to monitor and assess: (1) Changes in
the type and amount of HIV/AIDS health care and related services being
provided to each disproportionately impacted community of color; (2)
the aggregate number of persons receiving HIV/AIDS services within each
racial and ethnic community; and (3) the impact of Part A MAI-funded
services in terms of client-level and service-level health outcomes.
The information also is used to plan new technical assistance and
capacity development activities, and inform the HRSA policy and program
management functions. The data provided to HRSA does not contain
individual or personally identifiable information.
The annual estimated response burden for grantees is as follows:
--------------------------------------------------------------------------------------------------------------------------------------------------------
Estimated
Form number of Responses per Total Hours per Total burden
respondents respondent responses response hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Part A MAI Report.................................................. 56 2 112 5 560
--------------------------------------------------------------------------------------------------------------------------------------------------------
Note: Data collection system enhancements have resulted in a shortened response burden (from 6 to 5 total hours per response) for respondents since the
previous OMB approval request.
E-mail comments to paperwork@hrsa.gov or mail the HRSA Reports
Clearance Officer, Room 10-33, Parklawn Building, 5600 Fishers Lane,
Rockville, Maryland 20857. Written comments should be received within
30 days of this notice.
Dated: March 5, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information Coordination.
[FR Doc. 2010-5673 Filed 3-15-10; 8:45 am]
BILLING CODE 4165-15-P
