Proposed Data Collections Submitted for Public Comment and Recommendations, 37229-37230 [E9-17898]
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37229
Federal Register / Vol. 74, No. 143 / Tuesday, July 28, 2009 / Notices
next iteration of national health
promotion and disease prevention
objectives. Healthy People provides
science-based, 10-year national
objectives for promoting health and
preventing disease. Since 1979, Healthy
People has set and monitored national
health objectives to meet a broad range
of health needs, encourage
collaborations across sectors, guide
individuals toward making informed
health decisions, and measure the
impact of our prevention and health
promotion activities. Healthy People
2020 will reflect assessments of major
risks to health and wellness, changing
public health priorities, and emerging
issues related to our nation’s health
preparedness and prevention.
Public Participation at Meeting:
Members of the public are invited to
listen to the online Committee meeting.
There will be no opportunity for oral
public comments during the online
Committee meeting. Written comments,
however, are welcome throughout the
development process of the national
health promotion and disease
prevention objectives for 2020. They can
be submitted through the Healthy
People Web site at: https://
www.healthypeople.gov/hp2020/
comments/ or they can be e-mailed to
HP2020@hhs.gov. Please note that the
public comment Web site will be
updated throughout the Healthy People
development process, so people should
return to the site frequently and provide
their input.
To listen to the Committee meeting,
individuals must pre-register to attend
at the Healthy People Web site located
at https://www.healthypeople.gov.
Participation in the meeting is limited.
Registrations will be accepted until
maximum WebEx capacity is reached
and must be completed by 9 a.m. EDT
on August 14, 2009. A waiting list will
be maintained should registrations
exceed WebEx capacity. Individuals on
the waiting list will be contacted as
additional space for the meeting
becomes available.
Registration questions may be
directed to Hilary Scherer at
HP2020@norc.org (e-mail), (301) 634–
9374 (phone) or (301) 634–9301 (fax).
Dated: July 22, 2009.
Penelope Slade-Sawyer,
RADM, USPHS, Deputy Assistant Secretary
for Health (Disease Prevention and Health
Promotion).
[FR Doc. E9–17895 Filed 7–27–09; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: FPLS Child Support Services
Portal Registration (FCSSP).
OMB No.: New Collection.
Description: The Federal Office of
Child Support Enforcement (OCSE) is
implementing the Federal Parent
Locator Service (FPLS) Child Support
Services Portal (FCSSP) for users of the
FPLS to access online Web applications.
The portal Registration Process will
provide OCSE, States, employers and
multistate financial institutions the
ability to create a secure account to view
data for their respective applications. In
order for users to access the portal,
registration is required.
Respondents: OCSE, Employers,
Multistate Financial Institutions and
State Child Support Agencies.
Annual Burden Estimates
BILLING CODE 4150–32–P
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total
burden hours
Registration Screens: Employers, Financial Institutions and State Child
Support Agencies .................................................................................
mstockstill on DSKH9S0YB1PROD with NOTICES
Instrument
520
1
0.10
52
Estimated Total Annual Burden
Hours: 52.
Additional Information: Copies of the
proposed collection may be obtained 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. All requests
should be identified by the title of the
information collection. E-mail address:
infocollection@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Fax: 202–395–7245.
Attn: Desk Officer for the
VerDate Nov<24>2008
19:36 Jul 27, 2009
Jkt 217001
Administration for Children and
Families.
Dated: July 23, 2009.
Janean Chambers,
Reports Clearance Officer.
[FR Doc. E9–17886 Filed 7–27–09; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–09–08BN]
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
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
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 404–639–5960 and
send comments to Maryam I. Daneshvar,
CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS–D74, Atlanta,
GA 30333 or send an e-mail 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.
E:\FR\FM\28JYN1.SGM
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37230
Federal Register / Vol. 74, No. 143 / Tuesday, July 28, 2009 / Notices
Proposed Project
Voluntary Product Satisfaction and
Usability Assessment—New—National
Center for Injury Prevention and Control
(NCIPC), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Executive Order 12862 directs Federal
agencies that provide services directly
to the public to survey customers to
determine the kind and quality of
services they need and their level of
satisfaction with existing services.
CDC releases a number of new
products each year to its customers, a
diverse group that includes health care
providers, researchers, public health
practitioners, policy makers, and the
general public. The term product is
broadly defined to include publications,
Web pages, podcasts, e-cards, CD–
ROMs, and videos. At present, there is
no mechanism for evaluating whether
1. Response cards via mail: Each
product that is sent out will include a
one-page response card along with a
self-addressed and stamped envelope.
Customers can then voluntarily choose
whether to return the response card.
2. E-mail announcements: Products
are released to customers via an e-mail
announcement that includes a link to
the electronic version of the product
plus a link to a Web-based evaluation.
Customers can then voluntarily choose
whether to complete the evaluation.
3. Web-based assessments: Products
are available on-line in an electronic
format. Each product Web page will
include a link to a Web-based
evaluation. Customers can then
voluntarily choose whether to complete
the evaluation.
The information being collected will
not impose a cost burden on the
respondents beyond that associated
with their time to provide the required
data.
these products are meeting customer
needs.
CDC is requesting a 3-year generic
clearance in order to better evaluate its
products. Obtaining feedback from
customers on a regular, on-going basis
will help ensure that customers find
CDC products to be useful. This type of
evaluation will allow CDC to maximize
the impact of its products which will
ultimately benefit the public’s health.
The target audience will be limited to
customers who request and receive CDC
products. Customer participation in the
evaluation is completely voluntary.
Names of customers will not be
collected. The only personal
information collected will relate to
professional discipline, job duties, and
experience working with public health
topics. No sensitive data (e.g., age, race,
or gender) will be collected. The
evaluation data will be collected using
a combination of methodologies
including:
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Evaluation
method
Customers .....................
Response cards ...................................................
E-mail Assessments ............................................
Web-Based Assessments ...................................
50,000
60,000
432,000
1
1
1
10/60
10/60
10/60
8,333
10,000
72,000
Total ........................
..............................................................................
........................
........................
........................
90,333
Dated: July 22, 2009.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E9–17898 Filed 7–27–09; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
mstockstill on DSKH9S0YB1PROD with NOTICES
Office of Community Services; Notice
To Award a Single Source Program
Expansion Supplement Under the
American Recovery and Reinvestment
Act (ARRA) to Technical Assistance by
Community Action Program Legal
Services, Inc.
AGENCY: Office of Community Services,
ACF, HHS.
ACTION: Notice to award a Single Source
Program Expansion Supplement under
the American Recovery and
Reinvestment Act (ARRA) to Technical
Assistance by Community Action
Program Legal Services, Inc.
VerDate Nov<24>2008
19:36 Jul 27, 2009
Jkt 217001
Number of
respondents
Average
burden per
response
(in hours)
Type of respondent
CFDA#: 93.710.
Legislative Authority: The legislative
authority for this award is provided in the
American Recovery and Reinvestment Act of
2009 (Pub. L. 111–5). Additional legislative
authority and requirements are provided in
Section 674(b)(2)(B) of the CSBG Act, as
amended, by the Community Opportunity
Accountability, and Training and
Educational Services (Coats Human Services
Reauthorization Act of 1998) (Pub. L. 105–
285).
Amount of Supplemental Award:
$96,952.
Project Period: September 30, 2006
through September 30, 2009.
SUMMARY: The Office of Community
Services (OCS) announces the awarding
of a $96,952 single source program
expansion supplement to the
Community Action Legal Services, Inc.
(CAPLAW), located in Boston, MA, to
support training and technical
assistance on legal issues faced by
Community Action Agencies (CAAs)
related to the American Recovery and
Reinvestment Act of 2009 (ARRA). The
project activities are designed to support
and strengthen the ability of the CAA
network to comply with, and carry out,
PO 00000
Frm 00044
Fmt 4703
Sfmt 4703
Total burden
(in hours)
Community Services Block Grant
(CSBG) activities funded by ARRA. The
training projects and resources
developed under the award will include
analysis and explanation of the practical
impact of ARRA for States and CSBGeligible entities so that they can work
more effectively to reach the ARRA
goals and document how they have in
fact reached those goals and used the
ARRA funds. The project’s overall
approach is based on the following five
key elements: (1) Technical assistance
and issue-specific consultation; (2)
Publications, including online postings
on the CAPLAW Web site, e-Bulletins,
and a print newsletter, which is also
available on CAPLAW’s Web site; (3)
Online toolkit; (4) Presentations at CAA
conferences, including CAPLAW’s 2009
national training conference, and
CAPLAW audio conferences.
The training and technical assistance
CAPLAW will provide is particularly
critical at this time due to the large
temporary increase in funding of CSBG
awards to eligible entities and the need
for both rapid implementation of these
programs and adherence to high
E:\FR\FM\28JYN1.SGM
28JYN1
]]>Agencies
[Federal Register Volume 74, Number 143 (Tuesday, July 28, 2009)]
[Notices]
[Pages 37229-37230]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-17898]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-09-08BN]
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 404-639-5960
and send comments to Maryam I. Daneshvar, CDC Acting Reports Clearance
Officer, 1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send an e-mail
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.
[[Page 37230]]
Proposed Project
Voluntary Product Satisfaction and Usability Assessment--New--
National Center for Injury Prevention and Control (NCIPC), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Executive Order 12862 directs Federal agencies that provide
services directly to the public to survey customers to determine the
kind and quality of services they need and their level of satisfaction
with existing services.
CDC releases a number of new products each year to its customers, a
diverse group that includes health care providers, researchers, public
health practitioners, policy makers, and the general public. The term
product is broadly defined to include publications, Web pages,
podcasts, e-cards, CD-ROMs, and videos. At present, there is no
mechanism for evaluating whether these products are meeting customer
needs.
CDC is requesting a 3-year generic clearance in order to better
evaluate its products. Obtaining feedback from customers on a regular,
on-going basis will help ensure that customers find CDC products to be
useful. This type of evaluation will allow CDC to maximize the impact
of its products which will ultimately benefit the public's health.
The target audience will be limited to customers who request and
receive CDC products. Customer participation in the evaluation is
completely voluntary. Names of customers will not be collected. The
only personal information collected will relate to professional
discipline, job duties, and experience working with public health
topics. No sensitive data (e.g., age, race, or gender) will be
collected. The evaluation data will be collected using a combination of
methodologies including:
1. Response cards via mail: Each product that is sent out will
include a one-page response card along with a self-addressed and
stamped envelope. Customers can then voluntarily choose whether to
return the response card.
2. E-mail announcements: Products are released to customers via an
e-mail announcement that includes a link to the electronic version of
the product plus a link to a Web-based evaluation. Customers can then
voluntarily choose whether to complete the evaluation.
3. Web-based assessments: Products are available on-line in an
electronic format. Each product Web page will include a link to a Web-
based evaluation. Customers can then voluntarily choose whether to
complete the evaluation.
The information being collected will not impose a cost burden on
the respondents beyond that associated with their time to provide the
required data.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondent Evaluation method respondents responses per response (in (in hours)
respondent hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Customers...................................... Response cards......................... 50,000 1 10/60 8,333
E-mail Assessments..................... 60,000 1 10/60 10,000
Web-Based Assessments.................. 432,000 1 10/60 72,000
--------------------------------------------------------------------------------------------------------
Total...................................... ....................................... .............. .............. .............. 90,333
--------------------------------------------------------------------------------------------------------------------------------------------------------
Dated: July 22, 2009.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E9-17898 Filed 7-27-09; 8:45 am]
BILLING CODE 4163-18-P
