Proposed Information Collection Activity; Native Employment Works (NEW) Plan Guidance and NEW Program Report (OMB No.: 0970-0174), 16741-16742 [2022-06271]
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16741
Federal Register / Vol. 87, No. 57 / Thursday, March 24, 2022 / Notices
requirements, and goals of the statute.
Additionally, under 42 CFR 155.1200(b)
State Exchanges are required to provide
performance monitoring data to CMS.
State Exchanges must provide this data
at least annually and, in the manner,
format, and deadlines specified by HHS.
The information collection requirements
associated with these ICRs will
primarily involve programmatic
narrative, accompanying budget
narrative and appropriate supporting
documentation, and provision of
performance outcome and operational
data by grantees operating their
Exchanges. The SBEs are not required to
track or submit any personally
identifiable data. It is expected that
States will create data with readily
available word processing and
spreadsheet programs relying on source
data from information systems
developed from grant funding, ACA
section 1332 pass-through funding, or
state funding sources and submit such
information electronically. Form
Number: CMS–10371 (OMB control
number: 0938–1119); Frequency: Once;
Affected Public: State Government
agencies, non-profit entities; Number of
Respondents: 75; Number of Responses:
273; Total Annual Hours: 2,451. For
policy questions regarding this
collection contact Jenny Chen at (301)
492–5156 or Shilpa Gogna at (301) 492–
4257.
Dated: March 21, 2022.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2022–06213 Filed 3–23–22; 8:45 am]
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copies of the proposed collection of
information by emailing infocollection@
acf.hhs.gov. Identify all emailed
requests by the title of the information
collection.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Children’s Bureau National Youth in
Transition Database (NYTD); OMB
#0970–0340
SUPPLEMENTARY INFORMATION:
Children’s Bureau,
Administration for Children and
Families, HHS.
ACTION: Request for public comment.
AGENCY:
The Administration for
Children and Families (ACF) is
requesting a 3-year extension of the
National Youth in Transition Database
(NYTD) Youth Services Report and
Youth Outcomes Survey Data Collection
(OMB #0970–0340, expiration date 03/
31/2022). There are no changes
requested to the form.
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. You can also obtain
SUMMARY:
Description: The Foster Care
Independence Act of 1999 (42 U.S.C.
1305 et seq.) as amended by Public Law
106–169 requires state child welfare
agencies to collect and report to ACF
Children’s Bureau data on the
characteristics of youth receiving
independent living services and
information regarding their outcomes.
The regulation implementing the NYTD,
listed in 45 CFR 1356.80, contains
standard data collection and reporting
requirements for states to meet the law’s
requirements. Additionally, the Family
First Prevention Services Act of 2017
(H.R. 253) further outlines the
expectation of the collection and
reporting of data and outcomes
regarding youth who are in receipt of
independent living services. ACF uses
the information collected under the
regulation to track independent living
services, assess the collective outcomes
of youth, and potentially to evaluate
state performance with regard to those
outcomes consistent with the law’s
mandate.
Respondents: State agencies that
administer the Chafee Foster Care
Program for Successful Transition to
Adulthood (Chafee program) and youth
served by these agencies.
ANNUAL BURDEN ESTIMATES FOR 2022–2024
Total
number of
respondents
khammond on DSKJM1Z7X2PROD with NOTICES
Information collection title
Total
number of
responses per
respondent
Average
burden hours
per response
Total burden
hours for
2022–24
Annual
burden hours
State Data File .....................................................................
Youth Outcomes Survey ......................................................
52
47,000
2
1
3916
.5
407,264
23,500
135,755
7,833
Estimated Annual Burden Total ....................................
........................
........................
........................
........................
143,588
Estimated Total Annual Burden
Hours: 143,588.
Authority: NYTD is authorized by
Public Law 106–169, enacted December
14, 1999. This public law establishes the
John H. Chafee Foster Care
Independence Program, now known as
Chafee program, at section 477 of the
Social Security Act (the Act). NYTD
data are collected pursuant to 45 CFR
1356.80.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Mary B. Jones,
ACF/OPRE Certifying Officer.
Administration for Children and
Families
[FR Doc. 2022–06234 Filed 3–23–22; 8:45 am]
BILLING CODE 4184–01–P
Proposed Information Collection
Activity; Native Employment Works
(NEW) Plan Guidance and NEW
Program Report (OMB No.: 0970–0174)
Division of Tribal TANF
Management, Office of Family
AGENCY:
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16742
Federal Register / Vol. 87, No. 57 / Thursday, March 24, 2022 / Notices
Assistance, Administration for Children
and Families, HHS.
ACTION: Request for public comment.
The Administration for
Children and Families (ACF) is
requesting a 3-year extension of the
form OFA–0086: NEW Plan Guidance
and NEW Program Report (OMB #0970–
0174, expiration 8/31/2022). There are
minor changes requested to both
documents.
SUMMARY:
Comments due within 60 days of
publication. In compliance with the
requirements of the Paperwork
Reduction Act of 1995, ACF is soliciting
public comment on the specific aspects
DATES:
of the information collection described
above.
ADDRESSES: You can obtain copies of the
proposed collection of information and
submit comments by emailing
infocollection@acf.hhs.gov. Identify all
requests by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: The NEW Program Plan
Guidance documents specify the
information needed to complete a NEW
program plan and explain the process
for plan submission every third year and
to complete the annual program report.
The program plan is the application for
NEW program funding and documents
how the grantee will carry out its NEW
program. ACF proposes a change in how
draft plans are submitted. The program
report provides HHS, Congress, and
grantees information to document and
assess the activities and
accomplishments of the NEW program.
ACF proposes to extend data collection
with revisions that clarify that programs
should not count more than once
individuals who meet multiple
categories; for example, persons age 20
are both youth and adults, but they
should be counted as one or the other,
not both.
Respondents: Indian tribes and tribal
coalitions that operate NEW programs.
ANNUAL BURDEN ESTIMATES
Total number
of respondents
(over 3 yrs.)
Instrument
Average
burden hours
per response
Annual burden
hours
NEW Program Plan Guidance .........................................................................
NEW Program Report ......................................................................................
40
40
1 .333
1
29
15
386
600
Total Estimated Annual Burden ...............................................................
........................
........................
........................
986
1 We
have used .333 responses per year to represent one submission of the NEW Program Plan Guidance during the 3-year approval period.
Comments: 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) 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.
Authority: 42 U.S.C. 612.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2022–06271 Filed 3–23–22; 8:45 am]
BILLING CODE 4184–36–P
khammond on DSKJM1Z7X2PROD with NOTICES
Annual
number of
responses per
respondent
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17:39 Mar 23, 2022
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
796–3137, Kimberly.Lehrfeld@
fda.hhs.gov.
Food and Drug Administration
SUPPLEMENTARY INFORMATION:
[Docket No. FDA–2022–N–0352]
Secura Bio, Inc.; Withdrawal of
Approval of New Drug Application for
FARYDAK (Panobinostat) Capsules, 10
Milligrams, 15 Milligrams, and 20
Milligrams
Food and Drug Administration,
Health and Human Services (HHS).
ACTION: Notice.
AGENCY:
The Food and Drug
Administration (FDA or Agency) is
withdrawing approval of the new drug
application (NDA) for FARYDAK
(panobinostat) Capsules, 10 milligrams
(mg), 15 mg, and 20 mg, held by Secura
Bio, Inc., 1995 Village Center Circle,
Suite 128, Las Vegas, NV 89134. Secura
Bio, Inc. has voluntarily requested that
FDA withdraw approval of this
application and has waived its
opportunity for a hearing.
DATES: Approval is withdrawn as of
March 24, 2022.
FOR FURTHER INFORMATION CONTACT:
Kimberly Lehrfeld, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, Rm. 6226,
Silver Spring, MD 20993–0002, 301–
SUMMARY:
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On
February 23, 2015, FDA approved NDA
205353 for FARYDAK (panobinostat)
Capsules, 10 mg, 15 mg, and 20 mg, in
combination with bortezomib and
dexamethasone for the treatment of
patients with multiple myeloma who
have received at least two prior
regimens, including bortezomib and an
immunomodulatory agent, under the
Agency’s accelerated approval
regulations, 21 CFR part 314, subpart H.
The accelerated approval of FARYDAK
(panobinostat) Capsules, 10 mg, 15 mg,
and 20 mg, for multiple myeloma
included a required postmarketing trial
intended to verify the clinical benefit of
FARYDAK.
On September 24, 2021, FDA
published the Federal Register notice
‘‘Oncologic Drugs Advisory Committee;
Notice of Meeting; Establishment of a
Public Docket; Request for Comments,’’
announcing that FARYDAK
(panobinostat) Capsules would be
discussed at an Oncologic Drug
Advisory Committee Meeting (ODAC)
scheduled for December 2, 2021 (86 FR
53067). On November 19, 2021, FDA
met with Secura Bio, Inc. to discuss the
planned ODAC meeting. The topics
discussed included the lack of initiation
of the postmarketing trial intended to
verify clinical benefit.
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[Federal Register Volume 87, Number 57 (Thursday, March 24, 2022)]
[Notices]
[Pages 16741-16742]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-06271]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Native Employment Works
(NEW) Plan Guidance and NEW Program Report (OMB No.: 0970-0174)
AGENCY: Division of Tribal TANF Management, Office of Family
[[Page 16742]]
Assistance, Administration for Children and Families, HHS.
ACTION: Request for public comment.
-----------------------------------------------------------------------
SUMMARY: The Administration for Children and Families (ACF) is
requesting a 3-year extension of the form OFA-0086: NEW Plan Guidance
and NEW Program Report (OMB #0970-0174, expiration 8/31/2022). There
are minor changes requested to both documents.
DATES: Comments due within 60 days of publication. In compliance with
the requirements of the Paperwork Reduction Act of 1995, ACF is
soliciting public comment on the specific aspects of the information
collection described above.
ADDRESSES: You can obtain copies of the proposed collection of
information and submit comments by emailing [email protected].
Identify all requests by the title of the information collection.
SUPPLEMENTARY INFORMATION:
Description: The NEW Program Plan Guidance documents specify the
information needed to complete a NEW program plan and explain the
process for plan submission every third year and to complete the annual
program report. The program plan is the application for NEW program
funding and documents how the grantee will carry out its NEW program.
ACF proposes a change in how draft plans are submitted. The program
report provides HHS, Congress, and grantees information to document and
assess the activities and accomplishments of the NEW program. ACF
proposes to extend data collection with revisions that clarify that
programs should not count more than once individuals who meet multiple
categories; for example, persons age 20 are both youth and adults, but
they should be counted as one or the other, not both.
Respondents: Indian tribes and tribal coalitions that operate NEW
programs.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Total number Annual number Average burden
Instrument of respondents of responses hours per Annual burden
(over 3 yrs.) per respondent response hours
----------------------------------------------------------------------------------------------------------------
NEW Program Plan Guidance....................... 40 \1\ .333 29 386
NEW Program Report.............................. 40 1 15 600
---------------------------------------------------------------
Total Estimated Annual Burden............... .............. .............. .............. 986
----------------------------------------------------------------------------------------------------------------
\1\ We have used .333 responses per year to represent one submission of the NEW Program Plan Guidance during the
3-year approval period.
Comments: 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) 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.
Authority: 42 U.S.C. 612.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2022-06271 Filed 3-23-22; 8:45 am]
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