Agency Information Collection Activities; Proposed Collection; Comment Request; National Survey of Older Americans Act Participants, 74145-74146 [2013-29436]
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Federal Register / Vol. 78, No. 237 / Tuesday, December 10, 2013 / Notices
$28,785 for reporting + $46,080 for
disclosures).
Total annual capital or other nonlabor costs: $314,000, rounded to the
nearest thousand.
Total capital and start-up costs: The
Rule imposes no appreciable current
capital or start-up costs. The vast
majority of warrantors have already
developed systems to retain the records
and provide the disclosures required by
the Rule. Rule compliance does not
require the use of any capital goods,
other than ordinary office equipment, to
which providers already have access.
The Rule imposes only one additional
cost on IDSMs operating under the Rule
that would not apply to other IDSMs:
The annual audit requirement.
According to representatives of the
IDSMs, the vast majority of costs
associated with this requirement consist
of the fees paid to the auditors and their
staffs to perform the annual audit.
Representatives of the IDSMs previously
estimated a combined cost of $300,000
for both IDSMs currently operating
under the Rule. Staff retains that
estimate.
Other non-labor costs: $13,707 in
copying costs, based on estimated
copying costs of 7 cents per page and
several conservative assumptions. Staff
estimates that the average disputerelated file contains 35 pages and a
typical annual audit file contains
approximately 200 pages. As discussed
above, staff assumes that twenty percent
of consumers using an IDSM currently
operating under the Rule
(approximately 2,303 consumers)
request copies of the records relating to
their disputes.
Staff also estimates that a very small
minority of consumers request a copy of
the annual audit. Staff bases this
assumption on (1) the number of
consumer requests received by the
IDSMs in the past; and (2) the fact that
the IDSMs’ annual audits are available
online. For example, annual audits are
available on the FTC’s Web site, where
consumers may view and or print pages
as needed, at no cost to the IDSM. In
addition, the Better Business Bureau
makes available on its Web site the
annual audit of the BBB AUTO LINE.
Therefore, staff conservatively estimates
that only five percent of consumers
using an IDSM covered by the Rule
(approximately 576 consumers) will
request a copy of the IDSM’s audit
report.
Thus, the total annual copying cost
for dispute-related files is
approximately $5,643 (35 pages per file
× $.07 per page × 2,303 consumer
requests) and the total annual copying
cost for annual audit reports is
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approximately $8,064 (200 pages per
audit report × $.07 per page × 576
consumer requests). Accordingly, the
total cost attributed to copying under
the Rule is approximately $13,707.
Thus, the total non-labor cost under the
Rule is approximately $314,000
($300,000 for auditor fees + $13,707 for
copying costs).
Request for Comments
You can file a comment online or on
paper. Write ‘‘Warranty Rules:
Paperwork Comment, FTC File No.
P044403’’ on your comment. Your
comment—including your name and
your state—will be placed on the public
record of this proceeding, including, to
the extent practicable, on the public
Commission Web site, at https://
www.ftc.gov/os/publiccomments.shtm.
As a matter of discretion, the
Commission tries to remove individuals’
home contact information from
comments before placing them on the
Commission Web site.
Because your comment will be made
public, you are solely responsible for
making sure that your comment does
not include any sensitive personal
information, like anyone’s Social
Security number, date of birth, driver’s
license number or other state
identification number or foreign country
equivalent, passport number, financial
account number, or credit or debit card
number. You are also solely responsible
for making sure that your comment does
not include any sensitive health
information, like medical records or
other individually identifiable health
information. In addition, do not include
any ‘‘[t]rade secret or any commercial or
financial information which is * * *
privileged or confidential,’’ as discussed
in Section 6(f) of the FTC Act, 15 U.S.C.
46(f), and FTC Rule 4.10(a)(2), 16 CFR
4.10(a)(2). In particular, do not include
competitively sensitive information
such as costs, sales statistics,
inventories, formulas, patterns, devices,
manufacturing processes, or customer
names.
If you want the Commission to give
your comment confidential treatment,
you must file it in paper form, with a
request for confidential treatment, and
you must follow the procedure
explained in FTC Rule 4.9(c), 16 CFR
4.9(c).14 Your comment will be kept
confidential only if the FTC General
Counsel, in his or her sole discretion,
14 In particular, the written request for
confidential treatment that accompanies the
comment must include the factual and legal basis
for the request, and must identify the specific
portions of the comment to be withheld from the
public record. See FTC Rule 4.9(c), 16 CFR 4.9(c).
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74145
grants your request in accordance with
the law and the public interest.
Postal mail addressed to the
Commission is subject to delay due to
heightened security screening. As a
result, the Commission encourages you
to submit your comments online. To
make sure that the Commission
considers your online comment, you
must file it at https://
ftcpublic.commentworks.com/ftc/
idsrpra by following the instructions on
the web-based form. If this Notice
appears at https://www.regulations.gov,
you also may file a comment through
that Web site.
If you file your comment on paper,
write ‘‘Warranty Rules: Paperwork
Comment, FTC File No. P044403’’ on
your comment and on the envelope, and
mail or deliver it to the following
address: Federal Trade Commission,
Office of the Secretary, Room H–113
(Annex J), 600 Pennsylvania Avenue
NW., Washington, DC 20580. If possible,
submit your paper comment to the
Commission by courier or overnight
service.
Visit the Commission Web site at
https://www.ftc.gov to read this Notice.
The FTC Act and other laws that 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 on or
before February 10, 2014. You can find
more information, including routine
uses permitted by the Privacy Act, in
the Commission’s privacy policy, at
https://www.ftc.gov/ftc/privacy.htm.
David C. Shonka,
Principal Deputy General Counsel.
[FR Doc. 2013–29404 Filed 12–9–13; 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; National Survey of
Older Americans Act Participants
Administration for Community
Living, HHS.
ACTION: Notice.
AGENCY:
The Administration for
Community Living (ACL) 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
SUMMARY:
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maindgalligan on DSK5TPTVN1PROD with NOTICES
74146
Federal Register / Vol. 78, No. 237 / Tuesday, December 10, 2013 / Notices
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the information collection requirements
relating to the information collection
requirements contained in consumer
assessment surveys that are used by
ACL to measure program performance
for programs funded under Title III of
the Older Americans Act.
DATES: Submit written or electronic
comments on the collection of
information by February 10, 2014.
ADDRESSES: Submit electronic
comments on the collection of
information to: elena.fazio@acl.hhs.gov.
Submit written comments on the
collection of information to Elena Fazio,
Administration for Community Living,
Office of Performance and Evaluation,
Washington, DC 20201.
FOR FURTHER INFORMATION CONTACT:
Elena Fazio, 202–357–3583.
SUPPLEMENTARY INFORMATION: 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 request
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 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, ACL is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following collection
of information, ACL invites comments
on: (1) Whether the proposed collection
of information is necessary for the
proper performance of ACL’s functions,
including whether the information will
have practical utility; (2) the accuracy of
ACL’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
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18:48 Dec 09, 2013
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when appropriate, and other forms of
information technology.
The National Survey of Older
Americans Act (OAA) Participants
information collection, which builds on
earlier national pilot studies and
surveys, as well as performance
measurement tools developed by ACL
grantees in the Performance Outcomes
Measures Project (POMP), will include
consumer assessment surveys for the
Congregate and Home-delivered meal
nutrition programs; Case Management,
Homemaker, and Transportation
Services; and the National Family
Caregiver Support Program. This
information will be used by ACL to
track performance outcome measures;
support budget requests; comply with
GPRA Modernization Act of 2010
(GPRAMA) reporting requirements;
provide national benchmark
information; and inform program
development and management
initiatives. Descriptions of previous
National Surveys of OAA Participants
can be found under the section on OAA
Performance Information on ACL’s Web
site at: https://www.aoa.gov/AoARoot/
Program_Results/OAA_
Performance.aspx. Copies of the survey
instruments and data from previous
National Surveys of OAA Participants
can be found and queried using the
AGing Integrated Database (AGID) at
https://www.agid.acl.gov/. The proposed
Ninth National Survey entitled National
Survey of OAA Participants draft 2013
may be found on the ACL Web site at
https://www.aoa.gov/AoARoot/Program_
Results/OAA_Performance.aspx. ACL
estimates the burden of this collection
of information as follows: Respondents:
Individuals; Number of Respondents:
6,250; Number of Responses per
Respondent: one; Average Burden per
Response: 6000 at 40 minutes, 250 at 4
hours; Total Burden: 5,000.
Dated: December 5, 2013.
Kathy Greenlee,
Administrator and Assistant Secretary for
Aging.
[FR Doc. 2013–29436 Filed 12–9–13; 8:45 am]
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Food and Drug Administration
[Docket No. FDA–2013–N–0853]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Medical Devices
Current Good Manufacturing Practice
Quality System Regulation
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
(the PRA).
DATES: Fax written comments on the
collection of information by January 9,
2014.
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
comments should be identified with the
OMB control number 0910–0073. Also
include the FDA docket number found
in brackets in the heading of this
document.
SUMMARY:
FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 1350 Piccard
Dr., PI50–400B, Rockville, MD 20850,
PRAStaff@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.
FOR FURTHER INFORMATION CONTACT:
Medical Devices Current Good
Manufacturing Practice Quality System
Regulation—21 CFR Part 820 (OMB
Control Number 0910–0073)—Extension
Under section 520(f) of the Federal
Food, Drug, and Cosmetic Act (the
FD&C Act) (21 U.S.C. 360j(f)), the
Secretary of the Department of Health
and Human Services has the authority
to prescribe regulations requiring that
the methods used in, and the facilities
and controls used for, the manufacture,
preproduction design validation
(including a process to assess the
performance of a device but not
including an evaluation of the safety
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HUMAN SERVICES
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Agencies
[Federal Register Volume 78, Number 237 (Tuesday, December 10, 2013)]
[Notices]
[Pages 74145-74146]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-29436]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities; Proposed Collection;
Comment Request; National Survey of Older Americans Act Participants
AGENCY: Administration for Community Living, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Administration for Community Living (ACL) 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
[[Page 74146]]
publish notice in the Federal Register concerning each proposed
collection of information, including each proposed extension of an
existing collection of information, and to allow 60 days for public
comment in response to the notice. This notice solicits comments on the
information collection requirements relating to the information
collection requirements contained in consumer assessment surveys that
are used by ACL to measure program performance for programs funded
under Title III of the Older Americans Act.
DATES: Submit written or electronic comments on the collection of
information by February 10, 2014.
ADDRESSES: Submit electronic comments on the collection of information
to: elena.fazio@acl.hhs.gov.
Submit written comments on the collection of information to Elena
Fazio, Administration for Community Living, Office of Performance and
Evaluation, Washington, DC 20201.
FOR FURTHER INFORMATION CONTACT: Elena Fazio, 202-357-3583.
SUPPLEMENTARY INFORMATION: 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 request 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 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, ACL is publishing notice of the proposed collection
of information set forth in this document. With respect to the
following collection of information, ACL invites comments on: (1)
Whether the proposed collection of information is necessary for the
proper performance of ACL's functions, including whether the
information will have practical utility; (2) the accuracy of ACL'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.
The National Survey of Older Americans Act (OAA) Participants
information collection, which builds on earlier national pilot studies
and surveys, as well as performance measurement tools developed by ACL
grantees in the Performance Outcomes Measures Project (POMP), will
include consumer assessment surveys for the Congregate and Home-
delivered meal nutrition programs; Case Management, Homemaker, and
Transportation Services; and the National Family Caregiver Support
Program. This information will be used by ACL to track performance
outcome measures; support budget requests; comply with GPRA
Modernization Act of 2010 (GPRAMA) reporting requirements; provide
national benchmark information; and inform program development and
management initiatives. Descriptions of previous National Surveys of
OAA Participants can be found under the section on OAA Performance
Information on ACL's Web site at: https://www.aoa.gov/AoARoot/Program_Results/OAA_Performance.aspx. Copies of the survey instruments and
data from previous National Surveys of OAA Participants can be found
and queried using the AGing Integrated Database (AGID) at https://www.agid.acl.gov/. The proposed Ninth National Survey entitled National
Survey of OAA Participants draft 2013 may be found on the ACL Web site
at https://www.aoa.gov/AoARoot/Program_Results/OAA_Performance.aspx.
ACL estimates the burden of this collection of information as follows:
Respondents: Individuals; Number of Respondents: 6,250; Number of
Responses per Respondent: one; Average Burden per Response: 6000 at 40
minutes, 250 at 4 hours; Total Burden: 5,000.
Dated: December 5, 2013.
Kathy Greenlee,
Administrator and Assistant Secretary for Aging.
[FR Doc. 2013-29436 Filed 12-9-13; 8:45 am]
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