Submission for OMB Review; Social Services Block Grant (SSBG) Post-Expenditure Report, Pre-Expenditure Report, and Intended Use Plan (OMB #0970-0234), 14432-14433 [2021-05408]
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14432
Federal Register / Vol. 86, No. 49 / Tuesday, March 16, 2021 / Notices
Comments due within 30 days of
publication. OMB must make a decision
about 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.
DATES:
Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
ADDRESSES:
for Public Comments’’ or by using the
search function.
SUPPLEMENTARY INFORMATION:
Description: The PI, prepared in
response to the enactment of the CBCAP
program, as set forth in Title II of the
Child Abuse Prevention and Treatment
Reauthorization Act of 2010 (Public Law
111–320) or CAPTA, provides direction
to the states and territories to
accomplish the purposes of (1)
supporting community-based efforts to
develop, operate, expand, and where
appropriate to network, initiatives
aimed at the prevention of child abuse
and neglect, and to support networks of
coordinated resources and activities to
better strengthen and support families to
reduce the likelihood of child abuse and
neglect; and (2) fostering an
understanding, appreciation, and
knowledge of diverse populations in
order to be effective in preventing and
treating child abuse and neglect. This PI
contains information collection
requirements that are found in CAPTA
and pursuant to receiving a grant award.
The information submitted will be used
by the agency to ensure compliance
with the statute, complete the
calculation of the grant award
entitlement, and provide training and
technical assistance to the grantee.
Respondents: State governments,
quasi-public entities, and non-profit
private agencies.
ANNUAL BURDEN ESTIMATES
Instrument
Annual
number of
respondents
Annual number
of responses
per respondent
Average
burden hours
per response
Total annual
burden hours
Application .....................................................................................................
Annual Report ................................................................................................
52
52
1
1
40
24
2,080
1,248
Estimated Total Annual Burden
Hours: 3,328.
Authority: The CAPTA Reauthorization
Act of 2010; Title II of the CAPTA, Pub. L.
115–271 (42 U.S.C. 5116 et seq.).
Mary B.Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021–05411 Filed 3–15–21; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review; Social
Services Block Grant (SSBG) PostExpenditure Report, Pre-Expenditure
Report, and Intended Use Plan (OMB
#0970–0234)
Office of Community Services,
Administration for Children and
Families, HHS.
ACTION: Request for Public Comment.
AGENCY:
The Administration for
Children and Families (ACF) is
requesting a revision to the Social
Services Block Grant (SSBG) PostExpenditure Report, Pre-Expenditure
Report, and Intended Use Plan (OMB
#0970–0234, previously titled, ‘‘Social
Services Block Grant (SSBG) PostExpenditure Report’’). ACF is proposing
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SUMMARY:
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16:52 Mar 15, 2021
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to expand the information collection to
include the collection of states’
Intended Use Plans and retitle the
information collection to clarify the role
of the Pre-Expenditure Report.
DATES: Comments due within 30 days of
publication. OMB must make a decision
about 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.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
SUPPLEMENTARY INFORMATION:
Description: On an annual basis,
states and territories are required to
submit the following reports: (1) An
Intended Use Plan that provides data
and narrative descriptions related to the
state’s SSBG program. The Intended Use
Plan includes details about the delivery
of SSBG services, and the state agency
administering the SBG Program. ACF is
proposing to expand the currently
approved information collection to
include collection of states’ Intended
PO 00000
Frm 00030
Fmt 4703
Sfmt 4703
Use Plans. Grantees are required to
submit their Pre-Expenditure Report no
less than 30 days prior to the start of the
period covered by the report. (2) A PreExpenditure Report that demonstrates
the state’s anticipated allocation of
SSBG funding among the 29 pre-defined
SSBG service categories. Historically,
states have submitted this report using
the Post-Expenditure Report Form, and
the associated burden is included in the
currently approved information
collection. Grantees are required to
submit their Intended Use Plan no less
than 30 days prior to the start of the
period covered by the report. (3) A PostExpenditure Report that details the
state’s actual use of SSBG funding
among each of the 29 service categories.
Grantees are required to submit their
Post-Expenditure Report within 6
months of the end of the period covered
by the report.
Respondents: Agencies that
administer the SSBG at the state or
territory level, including the 50 states;
District of Columbia; Puerto Rico; and
the territories of American Samoa,
Guam, the Virgin Islands, and the
Commonwealth of Northern Mariana
Islands.
Annual Burden Estimates: This
request is specific to the Intended Use
Plan. Currently approved materials and
associated burden can be found at:
https://www.reginfo.gov/public/do/
PRAViewICR?ref_nbr=202011-0970-006.
E:\FR\FM\16MRN1.SGM
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14433
Federal Register / Vol. 86, No. 49 / Tuesday, March 16, 2021 / Notices
Instrument
Annual
number of
respondents
Annual number
of responses
per respondent
Average
burden hours
per response
Total/annual
burden hours
Intended Use Plan .........................................................................................
56
1
40
2,240.
acceptance receipt is on or before that
date.
Estimated Total Annual Burden
Hours: 2,240.
Authority: 42 U.S.C. 1397 through 1397e.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021–05408 Filed 3–15–21; 8:45 am]
BILLING CODE 4184–24–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–N–0547]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Survey on the
Occurrence of Foodborne Illness Risk
Factors in Selected Retail and
Foodservice Facility Types
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 ‘‘Survey on the
Occurrence of Foodborne Illness Risk
Factors in Selected Retail and
Foodservice Facility Types.’’
DATES: Submit either electronic or
written comments on the collection of
information by May 17, 2021.
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 May 17, 2021.
The https://www.regulations.gov
electronic filing system will accept
comments until 11:59 p.m. Eastern Time
at the end of May 17, 2021. Comments
received by mail/hand delivery/courier
(for written/paper submissions) will be
considered timely if they are
postmarked or the delivery service
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SUMMARY:
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Electronic Submissions
Submit electronic comments in the
following way:
• 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–
2012–N–0547 for ‘‘Agency Information
Collection Activities; Proposed
Collection; Comment Request; Survey
on the Occurrence of Foodborne Illness
Risk Factors in Selected Retail and
Foodservice Facility Types.’’ Received
comments, those filed in a timely
manner (see ADDRESSES), will be placed
in the docket and, except for those
submitted as ‘‘Confidential
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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, 240–402–7500.
• 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
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.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.pdf.
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, 240–402–7500.
FOR FURTHER INFORMATION CONTACT: Ila
S. Mizrachi, Office of Operations, Food
and Drug Administration, Three White
Flint North, 10A–12M, 11601
Landsdown St., North Bethesda, MD
20852, 301–796–7726, PRAStaff@
fda.hhs.gov.
Under the
PRA (44 U.S.C. 3501–3521), Federal
SUPPLEMENTARY INFORMATION:
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]]>Agencies
[Federal Register Volume 86, Number 49 (Tuesday, March 16, 2021)]
[Notices]
[Pages 14432-14433]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-05408]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Social Services Block Grant (SSBG)
Post-Expenditure Report, Pre-Expenditure Report, and Intended Use Plan
(OMB #0970-0234)
AGENCY: Office of Community Services, Administration for Children and
Families, HHS.
ACTION: Request for Public Comment.
-----------------------------------------------------------------------
SUMMARY: The Administration for Children and Families (ACF) is
requesting a revision to the Social Services Block Grant (SSBG) Post-
Expenditure Report, Pre-Expenditure Report, and Intended Use Plan (OMB
#0970-0234, previously titled, ``Social Services Block Grant (SSBG)
Post-Expenditure Report''). ACF is proposing to expand the information
collection to include the collection of states' Intended Use Plans and
retitle the information collection to clarify the role of the Pre-
Expenditure Report.
DATES: Comments due within 30 days of publication. OMB must make a
decision about 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.
ADDRESSES: Written comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function.
SUPPLEMENTARY INFORMATION:
Description: On an annual basis, states and territories are
required to submit the following reports: (1) An Intended Use Plan that
provides data and narrative descriptions related to the state's SSBG
program. The Intended Use Plan includes details about the delivery of
SSBG services, and the state agency administering the SBG Program. ACF
is proposing to expand the currently approved information collection to
include collection of states' Intended Use Plans. Grantees are required
to submit their Pre-Expenditure Report no less than 30 days prior to
the start of the period covered by the report. (2) A Pre-Expenditure
Report that demonstrates the state's anticipated allocation of SSBG
funding among the 29 pre-defined SSBG service categories. Historically,
states have submitted this report using the Post-Expenditure Report
Form, and the associated burden is included in the currently approved
information collection. Grantees are required to submit their Intended
Use Plan no less than 30 days prior to the start of the period covered
by the report. (3) A Post-Expenditure Report that details the state's
actual use of SSBG funding among each of the 29 service categories.
Grantees are required to submit their Post-Expenditure Report within 6
months of the end of the period covered by the report.
Respondents: Agencies that administer the SSBG at the state or
territory level, including the 50 states; District of Columbia; Puerto
Rico; and the territories of American Samoa, Guam, the Virgin Islands,
and the Commonwealth of Northern Mariana Islands.
Annual Burden Estimates: This request is specific to the Intended
Use Plan. Currently approved materials and associated burden can be
found at: https://www.reginfo.gov/public/do/PRAViewICR?ref_nbr=202011-0970-006.
[[Page 14433]]
----------------------------------------------------------------------------------------------------------------
Annual number of Average burden
Instrument Annual number responses per hours per Total/annual
of respondents respondent response burden hours
----------------------------------------------------------------------------------------------------------------
Intended Use Plan.......................... 56 1 40 2,240.
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 2,240.
Authority: 42 U.S.C. 1397 through 1397e.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021-05408 Filed 3-15-21; 8:45 am]
BILLING CODE 4184-24-P
