Att 2

Federal Register / Vol. 75, No. 100 / Tuesday, May 25, 2010 / Notices
A comment filed in paper form
should include the reference ‘‘Food
Industry Marketing to Children and
Adolescents Study: Paperwork
Comment; Project No. P094511’’ both in
the text and on the envelope, and
should be mailed or delivered to the
following address: Federal Trade
Commission, Office of the Secretary,
Room H-135 (Annex J), 600
Pennsylvania Avenue, N.W.,
Washington, D.C. 20580. The FTC is
requesting that any comment filed in
paper form be sent by courier or
overnight service, if possible, because
U.S. postal mail in the Washington area
and at the Commission is subject to
delay due to heightened security
precautions.
Comments on the proposed reporting
requirements, which are subject to OMB
review under the PRA, should
additionally be submitted to: Office of
Information and Regulatory Affairs,
Office of Management and Budget,
Attention: Desk Officer for Federal
Trade Commission. Comments should
be submitted via facsimile to (202) 3955167 because U.S. postal mail at the
OMB is subject to delays due to
heightened security precautions.
The FTC Act and other laws the
Commission administers permit the
collection of public comments to
consider and use in this proceeding as
appropriate. The Commission will
consider all timely and responsive
public comments that it receives,
whether filed in paper or electronic
form. Comments received will be
available to the public on the FTC
Website, to the extent practicable, at
(http://www.ftc.gov/os/
publiccomments.shtm). As a matter of
discretion, the FTC makes every effort to
remove home contact information for
individuals from the public comments it
receives before placing those comments
on the FTC Website. More information,
including routine uses permitted by the
Privacy Act, may be found in the FTC’s
privacy policy, at (http://www.ftc.gov/
ftc/privacy.shtm).
David C. Shonka,
Acting General Counsel.
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[FR Doc. 2010–12511 Filed 5–24–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day–10–10DT]

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 Daneshvar,
CDC 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.
Proposed Project
Monitoring and Reporting System for
Chronic Disease Prevention and Control
Programs—New—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Chronic diseases are the leading
causes of death and disability in the
United States, accounting for seven of
every ten deaths and affecting the
quality of life for 90 million Americans.
Chronic diseases represent 83% of all
U.S. health care spending.
The National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP) provides
funding to health departments in States,
territories, and the District of Columbia
to implement and evaluate chronic

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disease prevention and control
programs. Traditionally, support has
been provided through cooperative
agreements that are specific to a chronic
disease or condition. In 2009, CDC
announced a new cooperative
agreement program for collaborative
chronic disease prevention and health
promotion programs (RFA DP09–901;
authorized under sections 301, 307, 310,
and 311 of the Public Health Service Act
[42 U.S.C. 241 and 247(b)(k)). The new
program streamlines funding,
communication and collaboration in
four areas that have previously been
funded and evaluated independently:
Tobacco control, diabetes prevention
and control, State-based surveillance
through the Behavioral Risk Factor
Surveillance System (BRFSS), and the
Healthy Communities initiative.
Awardees are the 50 States, the District
of Columbia, Puerto Rico, and the Virgin
Islands. The new cooperative agreement
encourages each awardee to collaborate
with partners (both internal and
external to the State health department)
to develop and implement a multi-year,
statewide strategic plan.
CDC requests OMB approval to collect
information from the four specified
State programs through a new,
electronic Management Information
System (MIS). Upon approval, the new
information collection system will
replace two previously approved
information collections for tobacco
control programs (OMB No. 0920–0601,
exp. 5/31/2010), and diabetes
prevention and control programs (OMB
No. 0920–0479, exp. 4/30/2013), and
harmonize their content. In addition,
the new MIS will provide a common
progress reporting framework for Statebased BRFSS programs and Healthy
Community programs, which have
previously reported progress
information to CDC using standard
progress reporting forms for cooperative
agreement awardees (OMB No. 4040–
0004, exp. 3/31/2012).
Information will be collected on each
program’s objectives, planning
activities, resources, partnerships,
policy and environmental strategies for
preventing or controlling chronic
diseases, and progress toward meeting
goals. The increased emphasis on
partnership and collaboration is
intended to identify priorities, gaps in
chronic disease prevention and health
promotion activities, and opportunities
to leverage CDC and State (Federal and
non-Federal) resources. Information will
be collected electronically through a
new Management Information System
(MIS). The collection of information, in
a uniform and efficient manner, will
reduce duplicative reporting

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Federal Register / Vol. 75, No. 100 / Tuesday, May 25, 2010 / Notices

requirements for awardees, minimize
respondent burden, facilitate
collaborative efforts and provide
common performance metrics across
program areas. The collaborative
cooperative agreement is part of an
initiative within NCCDPHP to
standardize and streamline the funding
and performance monitoring processes
for programs funded through the Center;
to promote more efficient ways to use
resources; and to achieve greater health
impact. The objectives for awardees,
and the performance indicators defined
for them, reflect CDC’s support for more
integrated approaches to the prevention
and control of chronic conditions.
Awardees will use the information
collection to manage and coordinate

and control strategies implemented by
awardees. CDC will also use the
information collection to respond to
Congressional and stakeholder inquiries
about chronic disease control activities,
program implementation, and program
impact. Finally, the information
collection will allow CDC to evaluate
the success of the collaborative funding
model which places increased emphasis
on partnerships as well as policy and
environmental strategies for preventing
and controlling chronic diseases.
Information will be collected from
each State-based program twice per
year. There are no costs to respondents
other than their time.

their activities and to improve their
efforts to prevent and control chronic
diseases. The MIS will allow awardees
to fulfill their reporting obligations
under the cooperative agreements in an
efficient manner by employing a single
instrument to collect necessary
information for both progress reports
and continuation applications including
work plans.
CDC will use the information
collected in the MIS to monitor each
awardee’s progress and to make
adjustments, as needed, in the type and
level of technical assistance provided to
them. The information collection will
allow CDC to oversee the use of Federal
funds, and identify and disseminate
information about successful prevention

ESTIMATED ANNUALIZED BURDEN TABLE
Number of
respondents

Type of respondents

State
State
State
State

Total burden

Diabetes Program ..................................................................................
Tobacco Program ...................................................................................
BRFSS Program ....................................................................................
Healthy Communities Program ..............................................................

53
53
53
53

2
2
2
2

6
6
6
6

636
636
636
636

Total ..........................................................................................................

........................

........................

........................

2,544

Carol Walker,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2010–12537 Filed 5–24–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection:
Comment Request

srobinson on DSKHWCL6B1PROD with NOTICES

Average
burden per
response
(in hours)

Number of
responses per
respondent

In compliance with the requirement
for opportunity for public comment on
proposed data collection projects
(section 3506(c)(2)(A) of Title 44, United
States Code, as amended by the
Paperwork Reduction Act of 1995, Pub.
L. 104–13), the Health Resources and
Services Administration (HRSA)
publishes periodic summaries of
proposed projects being developed for
submission to the Office of Management
and Budget (OMB) under the Paperwork
Reduction Act of 1995. To request more
information on the proposed project or
to obtain a copy of the data collection
plans and draft instruments, e-mail

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paperwork@hrsa.gov or call the HRSA
Reports Clearance Officer at (301) 443–
1129.
Comments are invited on: (a) The
proposed collection of information for
the proper performance of the functions
of the agency; (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.
Proposed Project: Healthcare Integrity
and Protection Data Bank for Final
Adverse Information on Health Care
Providers, Suppliers and Practitioners
(45 CFR 61) (OMB No. 0915–0239)—
[Extension]
This is a request for extension of OMB
approval of the information collections
contained in regulations found in 45
CFR part 61 governing the Healthcare
Integrity and Protection Data Bank
(HIPDB) and the forms to be used in
reporting information to and requesting
information from the HIPDB cleared
under OMB No. 0915–0239. The HIPDB

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is authorized by section 1128E of the
Social Security Act (hereinafter referred
to as section 1128E), as added by section
221(a) of the Health Insurance
Portability and Accountability Act of
1996. Section 1128E directs the
Secretary of Health and Human Services
(the Secretary) to establish a national
health care fraud and abuse data
collection program for the reporting and
disclosing of certain final adverse
actions (excluding settlements in which
no findings of liability have been made)
taken against health care providers,
suppliers, or practitioners. It also directs
the Secretary to maintain a database of
final adverse actions taken against
health care providers, suppliers, or
practitioners. The regulations
implementing section 1128E governing
the operation of the HIPDB are codified
at 45 CFR part 61. The HIPDB became
operational November 22, 1999.
Approval is requested to continue the
following reporting data collection and
disclosure requirements and the ensuing
HIPDB forms along with the
instructions. The recordkeeping,
reporting, and disclosure requirements
are specified in the regulations to
implement the HIPDB. The annual
estimate of burden is as follows:

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