Agency Information Collection Activities; Proposed Collection; Public Comment Request; Revision of a Currently Approved Information Collection (ICR-Rev); Title III Supplemental Form to the Financial Status Report (SF-425), 28068-28069 [2017-12755]
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28068
Federal Register / Vol. 82, No. 117 / Tuesday, June 20, 2017 / Notices
Agency Contact: For further
information or comments regarding this
supplemental action, contact Cynthia
LaCounte, U.S. Department of Health
and Human Services, Administration for
Community Living, Administration on
Aging, 330 C Street SW., Washington
DC 20201; telephone 202–795–7380;
email Cynthia.LaCounte@acl.hhs.gov.
Dated: June 13, 2017.
Daniel P. Berger,
Acting Administrator and Assistant Secretary
for Aging.
[FR Doc. 2017–12753 Filed 6–19–17; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Proposed Collection; Public
Comment Request; Revision of a
Currently Approved Information
Collection (ICR-Rev); Title III
Supplemental Form to the Financial
Status Report (SF–425)
Administration for Community
Living, HHS.
AGENCY:
ACTION:
Notice.
The Administration for
Community Living (ACL) is announcing
an opportunity for the public to
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 a 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 proposed action. This
notice solicits comments on a proposed
revision of an existing data collection
regarding the information collection
requirements relating to the Title III
Supplemental Form to the Financial
Status Report for all ACL/AoA Title III
Grantees.
SUMMARY:
Submit written or electronic
comments on the collection of
information by August 21, 2017.
sradovich on DSK3GMQ082PROD with NOTICES
DATES:
Submit electronic
comments on the collection of
information to: jesse.more@acl.hhs.gov.
Submit written comments on the
collection of information to the U.S.
Department of Health and Human
Services, Administration for
Community Living, Washington, DC
20201, Attention: Jesse E. Moore, Jr.
FOR FURTHER INFORMATION CONTACT:
Jesse E. Moore, Jr., Aging Services
Program Specialist, Administration for
Community Living, Washington, DC,
20201, 202–795–7578.
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 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 to provide a 60 day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension or
update of an existing collection of
information, before submitting the
collection to OMB for approval. To
comply with this requirement, ACL is
publishing the 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.
ADDRESSES:
Number of
respondents
Respondent/data collection activity
Purpose
The Title III Supplemental Form to
the Financial Status Report (SF–425) is
used by ACL/AoA for all grantees to
obtain a more detailed understanding of
how projects funded under Title III of
the Older Americans Act (OAA) of 1965,
as amended, are being administered,
and to ensure compliance with
legislative requirements, pertinent
Federal regulations and other applicable
instructions and guidelines issued by
the ACL. The level of data detail
necessary is not available through the
Federal Financial Status Report (SF–
425) form. The Title III Supplemental
Form provides necessary details on nonfederal required match, administration
expenditures, Older Relative Caregivers
expenditures, and Long Term Care
Ombudsman expenditures.
In addition to renewing OMB
approval of this data collection, minor
changes are being proposed to it to
reflect changes in statutory language
that occurred as a result of the 2016
reauthorization of the OAA.
Specifically, the term ‘‘Grandparents
Only’’ has been changed to ‘‘Older
Relative Caregivers,’’ the new term in
the OAA that describes this population
of eligible service recipients. Similarly,
the accompanying instructions for
completing the Title III Supplemental
Form to the Financial Status Report
were also modified to include this same
language. References in the Code of
Federal Regulation (CFR) have been
updated addressing financial reporting
requirements and non-substantive
technical edits have been made to the
instructions.
Data Burden
ACL estimates the burden of this
collection of information as follows: 56
State Units on Aging (SUA) respond
semi-annually which should have an
average estimated burden of 2 hours per
grantee for a total of 112 hours per
submission.
The proposed data collection tool may
be found on the ACL Web site for
review at: https://www.acl.gov/sites/
default/files/about-acl/2017-06/
ACL%20Title%20
III%20Supplemental%20Form%20
and%20Instructions%202017.pdf.
Responses
per
respondent
Hours per
response
Total annual
burden hours
Title III Supplemental Form to the Financial Status Report ............................
56
2/yr
2
224
Total ..........................................................................................................
56
2/yr
2
224
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Federal Register / Vol. 82, No. 117 / Tuesday, June 20, 2017 / Notices
Dated: June 13, 2017.
Daniel P. Berger,
Acting Administrator and Assistant Secretary
for Aging.
[FR Doc. 2017–12755 Filed 6–19–17; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–1119]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Food Canning
Establishment Registration, Process
Filing, and Recordkeeping for Acidified
Foods and Thermally Processed LowAcid Foods in Hermetically Sealed
Containers
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
announcing an opportunity for public
comment on the proposed collection of
certain information by the Agency.
Under the Paperwork Reduction Act of
1995 (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 information, and
to allow 60 days for public comment in
response to the notice. This notice
solicits comments on the information
collection provisions of reporting and
recordkeeping requirements for firms
that process acidified foods and
thermally processed low-acid foods in
hermetically sealed containers.
DATES: Submit either electronic or
written comments on the collection of
information by August 21, 2017.
ADDRESSES: You may submit comments
as follows. Please note that late,
untimely filed comments will not be
considered. Electronic comments must
be submitted on or before August 21,
2017. The https://www.regulations.gov
electronic filing system will accept
comments until midnight Eastern Time
at the end of August 21, 2017.
Comments received by mail/hand
delivery/courier (for written/paper
submissions) will be considered timely
if they are postmarked or the delivery
service acceptance receipt is on or
before that date.
sradovich on DSK3GMQ082PROD with NOTICES
SUMMARY:
Electronic Submissions
Submit electronic comments in the
following way:
VerDate Sep<11>2014
18:01 Jun 19, 2017
Jkt 241001
• Federal eRulemaking Portal:
https://www.regulations.gov/. Follow
the instructions for submitting
comments. Comments submitted
electronically, including attachments, to
https://www.regulations.gov/ will be
posted to the docket unchanged.
Because your comment will be made
public, you are solely responsible for
ensuring that your comment does not
include any confidential information
that you or a third party may not wish
to be posted, such as medical
information, your or anyone else’s
Social Security number, or confidential
business information, such as a
manufacturing process. Please note that
if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov/.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2013–N–1119 for ‘‘Agency Information
Collection Activities; Proposed
Collection; Comment Request; Food
Canning Establishment Registration,
Process Filing, and Recordkeeping for
Acidified Foods and Thermally
Processed Low-Acid Foods in
Hermetically Sealed Containers.’’
Received comments, those filed in a
timely manner (see ADDRESSES), will be
placed in the docket and, except for
those submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov/ or at the
Dockets Management Staff between 9
a.m. and 4 p.m., Monday through
Friday.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
PO 00000
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28069
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on
https://www.regulations.gov/. Submit
both copies to the Dockets Management
Staff. If you do not wish your name and
contact information to be made publicly
available, you can provide this
information on the cover sheet and not
in the body of your comments and you
must identify this information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://www.fda.gov/
regulatoryinformation/dockets/
default.htm.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov/ and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Dockets Management
Staff, 5630 Fishers Lane, Rm. 1061,
Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
JonnaLynn Capezzuto, Office of
Operations, Food and Drug
Administration, Three White Flint
North, 10A63, 11601 Landsdown St.,
North Bethesda, MD 20852, 301–796–
3794, PRAStaff@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
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 to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
E:\FR\FM\20JNN1.SGM
20JNN1
]]>Agencies
[Federal Register Volume 82, Number 117 (Tuesday, June 20, 2017)]
[Notices]
[Pages 28068-28069]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-12755]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities; Proposed Collection;
Public Comment Request; Revision of a Currently Approved Information
Collection (ICR-Rev); Title III Supplemental Form to the Financial
Status Report (SF-425)
AGENCY: Administration for Community Living, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Administration for Community Living (ACL) is announcing an
opportunity for the public to 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 a 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 proposed action. This notice solicits comments on a
proposed revision of an existing data collection regarding the
information collection requirements relating to the Title III
Supplemental Form to the Financial Status Report for all ACL/AoA Title
III Grantees.
DATES: Submit written or electronic comments on the collection of
information by August 21, 2017.
ADDRESSES: Submit electronic comments on the collection of information
to: jesse.more@acl.hhs.gov. Submit written comments on the collection
of information to the U.S. Department of Health and Human Services,
Administration for Community Living, Washington, DC 20201, Attention:
Jesse E. Moore, Jr.
FOR FURTHER INFORMATION CONTACT: Jesse E. Moore, Jr., Aging Services
Program Specialist, Administration for Community Living, Washington,
DC, 20201, 202-795-7578.
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 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 to provide a 60 day notice in the Federal
Register concerning each proposed collection of information, including
each proposed extension or update of an existing collection of
information, before submitting the collection to OMB for approval. To
comply with this requirement, ACL is publishing the 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.
Purpose
The Title III Supplemental Form to the Financial Status Report (SF-
425) is used by ACL/AoA for all grantees to obtain a more detailed
understanding of how projects funded under Title III of the Older
Americans Act (OAA) of 1965, as amended, are being administered, and to
ensure compliance with legislative requirements, pertinent Federal
regulations and other applicable instructions and guidelines issued by
the ACL. The level of data detail necessary is not available through
the Federal Financial Status Report (SF-425) form. The Title III
Supplemental Form provides necessary details on non-federal required
match, administration expenditures, Older Relative Caregivers
expenditures, and Long Term Care Ombudsman expenditures.
In addition to renewing OMB approval of this data collection, minor
changes are being proposed to it to reflect changes in statutory
language that occurred as a result of the 2016 reauthorization of the
OAA. Specifically, the term ``Grandparents Only'' has been changed to
``Older Relative Caregivers,'' the new term in the OAA that describes
this population of eligible service recipients. Similarly, the
accompanying instructions for completing the Title III Supplemental
Form to the Financial Status Report were also modified to include this
same language. References in the Code of Federal Regulation (CFR) have
been updated addressing financial reporting requirements and non-
substantive technical edits have been made to the instructions.
Data Burden
ACL estimates the burden of this collection of information as
follows: 56 State Units on Aging (SUA) respond semi-annually which
should have an average estimated burden of 2 hours per grantee for a
total of 112 hours per submission.
The proposed data collection tool may be found on the ACL Web site
for review at: https://www.acl.gov/sites/default/files/about-acl/2017-06/ACL%20Title%20III%20Supplemental%20Form%20and%20Instructions%202017.pdf.
----------------------------------------------------------------------------------------------------------------
Number of Responses per Hours per Total annual
Respondent/data collection activity respondents respondent response burden hours
----------------------------------------------------------------------------------------------------------------
Title III Supplemental Form to the Financial 56 2/yr 2 224
Status Report..................................
---------------------------------------------------------------
Total....................................... 56 2/yr 2 224
----------------------------------------------------------------------------------------------------------------
[[Page 28069]]
Dated: June 13, 2017.
Daniel P. Berger,
Acting Administrator and Assistant Secretary for Aging.
[FR Doc. 2017-12755 Filed 6-19-17; 8:45 am]
BILLING CODE 4154-01-P
