Agency Information Collection Activities; Proposed Collection; Comment Request; University Centers for Excellence in Developmental Disabilities Education, Research, and Service-Annual Report, 34106-34107 [2013-13421]
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Federal Register / Vol. 78, No. 109 / Thursday, June 6, 2013 / Notices
5. LIHEAP Program Integrity
Assessment Supplement—OMB
Control No. 0970–0075; and
6. LIHEAP Model Plan (Detailed and
Abbreviated)—OMB Control No.
0970–0075.
The content and annual burden
estimates for the above existing data
collections will remain unchanged. The
only modification is the instrument of
the data collections, which will now be
through OLDC.
The information is being collected for
the Department’s annual LIHEAP Report
to Congress. The data also provides
information about the need for LIHEAP
funds. Finally, the data are used in the
calculation of LIHEAP performance
measures under the Government
Performance and Results Act of 1993.
The data elements will improve the
accuracy of measuring LIHEAP targeting
performance and LIHEAP cost
efficiency.
Respondents: State Governments and
the District of Columbia
ANNUAL BURDEN ESTIMATES FOR PERFORMANCE MEASURES
mstockstill on DSK4VPTVN1PROD with NOTICES
Percentage of Reduction in Household Energy Burden .................
Number of Utility Service Restorations ............................................
Number of Crises Averted ...............................................................
Estimated Total Annual Burden
Hours: 5,100.
As LIHEAP is a block grant, there is
a wide spectrum of capacity to collect
and report data among grantees. The
estimated burden hours displayed above
are for the average LIHEAP grantee,
assuming data collection systems and
agreements already in place. For those
grantees that would need to establish
such agreements and systems, estimated
burden for the initial year of reporting
would more closely resemble 400 hours
for each performance measure.
However, after the systems are in place,
estimated burden for the collection of
these data will more closely reflect the
figures in the table above.
In compliance with the requirements
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Administration,
Office of Information Services, 370
L’Enfant Prmenade SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. Email address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.
The Department specifically requests
comments 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)
the quality, utility, and clarity of the
information to be collected; and (d)
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Number of
responses per
respondent
Number of
respondents
Performance measure
51
51
51
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.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2013–13384 Filed 6–5–13; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Proposed Collection;
Comment Request; University Centers
for Excellence in Developmental
Disabilities Education, Research, and
Service—Annual Report
The Administration on
Intellectual and Developmental
Disabilities (AIDD), Administration for
Community Living (ACL), HHS.
ACTION: Notice.
AGENCY:
The Administration on
Intellectual and Developmental
Disabilities (AIDD), now part of the
Administration for Community Living,
is announcing that the proposed
collection of information listed below
has been submitted to the Office of
Management and Budget (OMB) for
review and clearance under the
Paperwork Reduction Act of 1995.
DATES: Submit written comments on the
collection of information by July 8,
2013.
SUMMARY:
ADDRESSES:
OIRA_submission@omb.eop.gov or by
fax to 202.395.5806. Attn: OMB Desk
PO 00000
Frm 00076
Fmt 4703
Sfmt 4703
Average
burden hours
per response
1
1
1
60
20
20
Total burden
hours
3,060
1,020
1,020
Officer for ACL, Office of Information
and Regulatory Affairs, OMB.
FOR FURTHER INFORMATION CONTACT:
Jennifer Johnson, at 202–690–5982 or
jennifer.johnson@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, the
Administration on Intellectual and
Developmental Disabilities (now part of
the Administration for Community
Living) has submitted the following
proposed collection of information to
OMB for review and clearance.
Section 104 (42 U.S.C. 15004) of the
Developmental Disabilities Assistance
and Bill of Rights Act of 2000 (DD Act
of 2000) directs the Secretary of Health
and Human Services to develop and
implement a system of program
accountability to monitor the grantees
funded under the DD Act of 2000. The
program accountability system shall
include the National Network of
University Centers for Excellence in
Developmental Disabilities Education,
Research, and Service (UCEDDs)
authorized under Part D of the DD Act
of 2000. In addition to the
accountability system, Section 154 (e)
(42 U.S.C. 15064) of the DD Act of 2000
includes requirements for a UCEDD
Annual Report. In response to the 60day Federal Register notice related to
this proposed data collection and
published on January 15, 2013 in
Volume 78, ten sets of comments were
received. Most of the comments
provided recommendations for
enhancing the quality and clarity of the
information to be collected. The
comments resulted in some revisions to
the proposed data collection tools. The
originally proposed data collection
tools, the comments with responses and
a revised set of data collection tools may
be obtained by contacting Jennifer
Johnson at jennifer.johnson@acl.hhs.gov
or 202–690–5982. AIDD estimates the
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Federal Register / Vol. 78, No. 109 / Thursday, June 6, 2013 / Notices
burden of this collection of information
as 1,412 average burden hours per
responses, for 67 UCEDDs—Total
burden is 94,604 hours per year.
Dated: June 3, 2013.
Kathy Greenlee,
Administrator and Assistant Secretary for
Aging.
[FR Doc. 2013–13421 Filed 6–5–13; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0190]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Requirements
Under the Comprehensive Smokeless
Tobacco Health Education Act of 1986,
as Amended by the Family Smoking
Prevention and Tobacco Control Act
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by July 8,
2013.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or emailed to
oira_submission@omb.eop.gov. All
SUMMARY:
comments should be identified with the
OMB control number 0910–0671. Also
include the FDA docket number found
in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT:
Daniel Gittleson, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
5156, daniel.gittleson@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
Requirements Under the
Comprehensive Smokeless Tobacco
Health Education Act of 1986, as
Amended by the Family Smoking
Prevention and Tobacco Control Act—
(OMB Control Number 0910–0671)—
Extension
On June 22, 2009, the President
signed the Family Smoking Prevention
and Tobacco Control Act (the Tobacco
Control Act) (Pub. L. 111–31) into law.
Section 3 of the Comprehensive
Smokeless Tobacco Health Education
Act of 1986 (the Smokeless Tobacco
Act) (15 U.S.C. 4402), as amended by
section 204 of the Tobacco Control Act,
requires, among other things, that all
smokeless tobacco product packages
and advertisements bear one of four
required warning statements. Section
3(b)(3)(A) of the Smokeless Tobacco Act
requires that the warnings be displayed
on packaging and advertising for each
brand of smokeless tobacco ‘‘in
accordance with a plan submitted by the
tobacco product manufacturer, importer,
distributor, or retailer’’ to, and approved
by, FDA.
This information collection—the
submission to FDA of warning plans for
smokeless tobacco products—is
statutorily mandated. The warning
plans will be reviewed by FDA, as
required by the Smokeless Tobacco Act,
to determine whether the companies’
plans for the equal distribution and
display of warning statements on
packaging and the quarterly rotation of
warning statements in advertising for
each brand of smokeless tobacco
products comply with section 3 of the
Smokeless Tobacco Act, as amended.
Based on the Federal Trade
Commission’s (FTC’s) previous
experience with the submission of
warning plans and FDA’s experience
with smokeless tobacco companies (e.g.,
correspondence associated with user
fees under section 919 of the Federal
Food, Drug, and Cosmetic Act, as
amended by the Tobacco Control Act
(21 U.S.C. 387s)), FDA estimates that
there are 36 companies affected by this
information collection. To account for
the entry of new smokeless tobacco
companies that may be affected by this
information collection, FDA is
estimating the total number of
respondents to be 100.
When the FTC requested an extension
of their approved information collection
in 2007, based on over 20 years
implementing the warning plan
requirements and taking into account
increased computerization and
improvements in electronic
communication, the FTC estimated
submitting an initial plan would take 60
hours. Based on FDA’s experience over
the past several years, FDA believes the
estimate of 60 hours to complete an
initial rotational plan continues to be
reasonable.
In the Federal Register of March 18,
2013 (78 FR 16678), FDA published a
60-day notice requesting public
comment on the proposed collection of
information. No comments were
received.
FDA estimates the burden of this
collection of information as follows:
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN 1
Activity
Number of
respondents
Number of
responses per
respondent
Total annual
responses
Average
burden per
response
Total hours
Total capital
costs
Submission of rotational plans for health
warning label statements .....................
100
1
100
60
6,000
$1,200
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1 There
are no operating and maintenance costs associated with this collection of information.
FDA estimates a total of 100
respondents at 1 response each and 60
burden hours per response for a total of
6,000 burden hours (100 respondents ×
1 response × 60 burden hours = 6,000
total burden hours). In addition, capital
costs are based on all 100 respondents
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mailing in their submission at a postage
rate of $12 for a 5-pound parcel
(business parcel post mail delivered
from the farthest delivery zone).
Therefore, FDA estimates that the total
postage cost for mailing the rotational
warning plans to be $1,200.
PO 00000
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Dated: June 3, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013–13448 Filed 6–5–13; 8:45 am]
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Agencies
[Federal Register Volume 78, Number 109 (Thursday, June 6, 2013)]
[Notices]
[Pages 34106-34107]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-13421]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities; Proposed Collection;
Comment Request; University Centers for Excellence in Developmental
Disabilities Education, Research, and Service--Annual Report
AGENCY: The Administration on Intellectual and Developmental
Disabilities (AIDD), Administration for Community Living (ACL), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Administration on Intellectual and Developmental
Disabilities (AIDD), now part of the Administration for Community
Living, is announcing that the proposed collection of information
listed below has been submitted to the Office of Management and Budget
(OMB) for review and clearance under the Paperwork Reduction Act of
1995.
DATES: Submit written comments on the collection of information by July
8, 2013.
ADDRESSES: OIRA_submission@omb.eop.gov or by fax to 202.395.5806.
Attn: OMB Desk Officer for ACL, Office of Information and Regulatory
Affairs, OMB.
FOR FURTHER INFORMATION CONTACT: Jennifer Johnson, at 202-690-5982 or
jennifer.johnson@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, the
Administration on Intellectual and Developmental Disabilities (now part
of the Administration for Community Living) has submitted the following
proposed collection of information to OMB for review and clearance.
Section 104 (42 U.S.C. 15004) of the Developmental Disabilities
Assistance and Bill of Rights Act of 2000 (DD Act of 2000) directs the
Secretary of Health and Human Services to develop and implement a
system of program accountability to monitor the grantees funded under
the DD Act of 2000. The program accountability system shall include the
National Network of University Centers for Excellence in Developmental
Disabilities Education, Research, and Service (UCEDDs) authorized under
Part D of the DD Act of 2000. In addition to the accountability system,
Section 154 (e) (42 U.S.C. 15064) of the DD Act of 2000 includes
requirements for a UCEDD Annual Report. In response to the 60-day
Federal Register notice related to this proposed data collection and
published on January 15, 2013 in Volume 78, ten sets of comments were
received. Most of the comments provided recommendations for enhancing
the quality and clarity of the information to be collected. The
comments resulted in some revisions to the proposed data collection
tools. The originally proposed data collection tools, the comments with
responses and a revised set of data collection tools may be obtained by
contacting Jennifer Johnson at jennifer.johnson@acl.hhs.gov or 202-690-
5982. AIDD estimates the
[[Page 34107]]
burden of this collection of information as 1,412 average burden hours
per responses, for 67 UCEDDs--Total burden is 94,604 hours per year.
Dated: June 3, 2013.
Kathy Greenlee,
Administrator and Assistant Secretary for Aging.
[FR Doc. 2013-13421 Filed 6-5-13; 8:45 am]
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