Submission for OMB Review; Unaccompanied Children (UC) Program Budget Workbook Template (New Collection), 72602-72603 [2021-27767]
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Federal Register / Vol. 86, No. 243 / Wednesday, December 22, 2021 / Notices
• Disseminate insights related to
human trafficking cases and trends to
inform anti-trafficking strategies and
policies; and
• Provide information to Congress,
other federal agencies, stakeholders, the
public, and other countries on the
aggregate outputs and outcomes of the
NHTH operations.
In accordance with the Paperwork
Reduction Act of 1995 (Pub. L. 104–13)
and OMB regulations at 5 CFR part
1320, ACF published a notice in the
Federal Register to announce the
agency’s intention to request OMB
review of this information collection
activity and provide a sixty-day period
for public comment (86 FR 38489).
During the notice and comment period,
one comment was received from the
NHTH grantee. The comment did not
pertain to the burden estimate for
respondents (signalers to the NHTH),
rather the burden on the recordkeeper
(the NHTH grantee).
To be responsive to this comment and
reduce the burden on the recordkeeper,
OTIP modified the collection to remove
several of the data elements that were
initially proposed. Where OTIP has
requested any new data (e.g., data the
grantee is not already providing to OTIP
as a condition of award), particularly,
for existing data to be further
disaggregated, it is in the interest of
allowing OTIP to:
• Monitor performance and
operational issues;
• Generate more timely insights into
trends related to victim demographics
and service needs, and the impact of
particular intra- and inter-agency efforts,
messaging campaigns, trainings, and
other anti-trafficking efforts on NHTH
signals, and;
• Respond to congressional inquiries
and other ad hoc inquiries without
submitting burdensome individual
requests to the NHTH.
Respondents: Potential victims,
representatives of governmental entities,
law enforcement, first responders,
members of the community,
representatives of nongovernmental
entities providing social, legal, or
protective services to individuals in the
United States who may have been
subjected to severe forms of trafficking
in persons utilize the NHTH as
signalers.
ANNUAL BURDEN ESTIMATES
Instrument
Total
number of
respondents
(signalers)
Total
number of
responses per
respondent
Average
burden hours
per response
Total
burden hours
Annual
burden hours
585,300
1
0.43333333
253,630
84,543
National Human Trafficking Hotline (NHTH) Performance
Indicators ..........................................................................
Estimated Total Annual Burden
Hours: 84,543.
Authority: 22 U.S.C. 7105.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021–27646 Filed 12–21–21; 8:45 am]
BILLING CODE 4184–47–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Unaccompanied Children (UC)
Program Budget Workbook Template
(New Collection)
Office of Refugee Resettlement,
Administration for Children and
Families, HHS.
ACTION: Request for public comment.
AGENCY:
The Administration for
Children and Families’ (ACF) Office of
Refugee Resettlement (ORR) is
requesting clearance for the proposed
new collection titled ‘‘UC Program
Budget Workbook’’ to streamline budget
details and justifications of applicants to
funding opportunities.
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.
SUMMARY:
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
ADDRESSES:
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
SUPPLEMENTARY INFORMATION:
Description: The UC Program Budget
Workbook will streamline the budget
detail and justification documentation
for applicants to any upcoming Notice
of Funding Opportunity (NOFO). This
new information collection will provide
guidance to the applicant as well as a
fillable form to insert calculations and
budget line items. With the assistance of
this template, the review of applications
will be expedited since documentation
will be clearer and more unified.
Additionally, this will facilitate the
completion of applications that may not
otherwise be completed due to lack of
budget documentation guidance in past
NOFOs.
Respondents: New and existing
applicants to NOFOs for residential
services for UC.
khammond on DSKJM1Z7X2PROD with NOTICES
ANNUAL BURDEN ESTIMATES
Instrument
Total
number of
respondents
Total
number of
responses per
respondent
Average
burden
hours per
response
Total
burden
hours
Annual
burden
hours
UC Program Budget Form ...................................................
120
3
90
32,400
10,800
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Federal Register / Vol. 86, No. 243 / Wednesday, December 22, 2021 / Notices
Estimated Total Annual Burden
Hours: 10,800.
Authority: 8 U.S.C. 1522 of the
Immigration and Nationality Act (the Act)
(Title IV, Sec. 412 of the Act) and 45 CFR
400.28(b).
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021–27767 Filed 12–21–21; 8:45 am]
BILLING CODE 4184–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2021–D–0756]
Validation and Verification of
Analytical Testing Methods Used for
Tobacco Products; Draft Guidance for
Industry; Availability; Request for
Comments
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice; request for comments.
The Food and Drug
Administration (FDA, Agency, or we) is
announcing the availability of a draft
guidance for industry entitled
‘‘Validation and Verification of
Analytical Testing Methods used for
Tobacco Products’’ and requesting
comments, including scientific and
other information, concerning the
recommendations set forth in the draft
guidance. The draft guidance, when
finalized, would provide information
and recommendations related to the
validation and verification of analytical
test methods, including analytical
testing of tobacco product constituents,
ingredients, and additives, as well as
stability testing of tobacco products.
This draft guidance would help industry
produce more consistent and reliable
analytical data used to support
regulatory submissions for finished
tobacco products.
DATES: Submit either electronic or
written comments on the draft guidance
by February 22, 2022 to ensure that the
Agency considers your comment on this
draft guidance before it begins work on
the final version of the guidance.
ADDRESSES: You may submit comments
on any guidance at any time as follows:
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
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://
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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–
2021–D–0756 for ‘‘Validation and
Verification of Analytical Testing
Methods used for Tobacco Products.’’
Received comments 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, 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
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72603
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.
You may submit comments on any
guidance at any time (see 21 CFR
10.115(g)(5)).
Submit written requests for single
copies of the draft guidance to the
Center for Tobacco Products, Food and
Drug Administration, 10903 New
Hampshire Ave., Document Control
Center, Bldg. 71, Rm. G335, Silver
Spring, MD 20993–0002. Send one selfaddressed adhesive label to assist that
office in processing your request or
include a fax number to which the
guidance document may be sent. See the
SUPPLEMENTARY INFORMATION section for
electronic access to the draft guidance
document.
FOR FURTHER INFORMATION CONTACT:
Nathan Mease or Matthew Brenner,
Center for Tobacco Products, Food and
Drug Administration, Document Control
Center, 10903 New Hampshire Ave.,
Bldg. 71, Rm. G335, Silver Spring, MD
20993–0002, 1–877–287–1373, email:
CTPRegulations@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
We are announcing the availability of
a draft document entitled ‘‘Validation
and Verification of Analytical Testing
Methods used for Tobacco Products;
Draft Guidance for Industry.’’ This draft
guidance, when finalized, provides
information and recommendations on
how tobacco product manufacturers can
produce validation and verification data
for the analytical procedures and
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]]>Agencies
[Federal Register Volume 86, Number 243 (Wednesday, December 22, 2021)]
[Notices]
[Pages 72602-72603]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-27767]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Unaccompanied Children (UC) Program
Budget Workbook Template (New Collection)
AGENCY: Office of Refugee Resettlement, Administration for Children and
Families, HHS.
ACTION: Request for public comment.
-----------------------------------------------------------------------
SUMMARY: The Administration for Children and Families' (ACF) Office of
Refugee Resettlement (ORR) is requesting clearance for the proposed new
collection titled ``UC Program Budget Workbook'' to streamline budget
details and justifications of applicants to funding opportunities.
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: The UC Program Budget Workbook will streamline the
budget detail and justification documentation for applicants to any
upcoming Notice of Funding Opportunity (NOFO). This new information
collection will provide guidance to the applicant as well as a fillable
form to insert calculations and budget line items. With the assistance
of this template, the review of applications will be expedited since
documentation will be clearer and more unified. Additionally, this will
facilitate the completion of applications that may not otherwise be
completed due to lack of budget documentation guidance in past NOFOs.
Respondents: New and existing applicants to NOFOs for residential
services for UC.
Annual Burden Estimates
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total number of Average burden
Instrument Total number of responses per hours per Total burden Annual burden
respondents respondent response hours hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
UC Program Budget Form............................................. 120 3 90 32,400 10,800
--------------------------------------------------------------------------------------------------------------------------------------------------------
[[Page 72603]]
Estimated Total Annual Burden Hours: 10,800.
Authority: 8 U.S.C. 1522 of the Immigration and Nationality Act
(the Act) (Title IV, Sec. 412 of the Act) and 45 CFR 400.28(b).
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021-27767 Filed 12-21-21; 8:45 am]
BILLING CODE 4184-45-P
