Proposed Information Collection Activity; State Plan for Grants to States for Refugee Resettlement (Office of Management and Budget #0970-0351), 75289-75290 [2023-24185]
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75289
Federal Register / Vol. 88, No. 211 / Thursday, November 2, 2023 / Notices
ANNUAL BURDEN ESTIMATES
Total
number of
respondents
Instrument
RFP and Contract ................................................................
Emergency Funding Request ..............................................
Biennial Reports ...................................................................
Advance Planning Document ..............................................
Operational Advance Planning Document ...........................
Independent Verification and Validation (ongoing) ..............
Independent Verification and Validation (semiannually) .....
Independent Verification and Validation (quarterly) ............
System Certification .............................................................
Estimated Total Annual Burden
Hours: 9,158.50.
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: 45 CFR part 95, subpart F.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2023–24211 Filed 11–1–23; 8:45 am]
BILLING CODE 4184–41–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; State Plan for Grants to States
for Refugee Resettlement (Office of
Management and Budget #0970–0351)
Office of Refugee Resettlement,
Administration for Children and
AGENCY:
Total
number of
responses per
respondent
50
21
54
44
10
3
4
10
3
Average
burden hours
per response
4.5
1
1.5
3.6
3
12
6
12
3
Families, U.S. Department of Health and
Human Services.
ACTION: Request for public comments.
The Administration for
Children and Families (ACF), Office of
Refugee Resettlement (ORR) is
requesting a 3-year extension of the
State Plan for Grants to States for
Refugee Resettlement (Office of
Management and Budget #0970–0351,
expiration 6/30/2024). ORR is proposing
changes to the form.
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
infocollection@acf.hhs.gov. Identify all
requests by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: A State Plan is a required
comprehensive narrative description of
the nature and scope of a state’s or
Replacement Designee’s (RD) Refugee
Resettlement Program and provides
assurances that the program will be
administered in conformity with the
specific requirements stipulated in 45
CFR 400.4–400.9. The State Plan must
include all applicable state or RD
procedures, designations, and
certifications for each requirement as
well as supporting documentation. The
SUMMARY:
4
2
1.5
120
30
10
16
30
240
Total
burden hours
900
42
121.5
19,008
900
360
384
3,600
2,160
Annual
burden hours
300
14
40.5
6,336
300
120
128
1,200
720
plan assures ORR that the state or RD is
capable of administering refugee
assistance and coordinating
employment and other social services
for eligible caseloads in conformity with
specific requirements.
ORR proposes the following changes
to the previously approved State Plan
for Grants to States for Refugee
Resettlement:
• streamlining/formatting multiple
sections of the form, including
technical corrections
• enhancing requirements for
collaboration and engagement and
expanding the non-discrimination
aspects
• standardizing sections of the template
related to health to reduce burden by
clarifying text and removing
duplicative parts
• streamlining sections related to the
unaccompanied children to reduce
burden by providing better options for
responses and selections and by
removing unnecessary and confusing
text to ensure consistency regarding
assurances
Respondents: State agencies and RDs
under 45 CFR 400.301(c) administering
or supervising the administration of
programs.
khammond on DSKJM1Z7X2PROD with NOTICES
ANNUAL BURDEN ESTIMATES
Instrument
Total
number of
respondents
Annual
number of
responses per
respondent
Average
burden hours
per response
Annual
burden hours
State Plan for Grants to States for Refugee Resettlement .............................
59
1
18
1,062
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E:\FR\FM\02NON1.SGM
02NON1
75290
Federal Register / Vol. 88, No. 211 / Thursday, November 2, 2023 / Notices
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: 8 U.S.C. 1522 of the
Immigration and Nationality Act (the
Act) [Title IV, Sec. 412 of the Act] for
each state agency requesting federal
funding for refugee resettlement under 8
U.S.C. 524 [Title IV, Sec. 414 of the
Act].
Mary Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2023–24185 Filed 11–1–23; 8:45 am]
BILLING CODE 4184–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2019–N–2809]
Advisory Committee; Patient
Engagement Advisory Committee;
Renewal
AGENCY:
Food and Drug Administration,
HHS.
Notice; renewal of Federal
advisory committee.
ACTION:
The Food and Drug
Administration (FDA or the Agency) is
announcing the renewal of the Patient
Engagement Advisory Committee by the
Commissioner of Food and Drugs (the
Commissioner). The Commissioner has
determined that it is in the public
interest to renew the Patient
Engagement Advisory Committee for an
additional 2 years beyond the charter
expiration date. The new charter will be
in effect until the October 6, 2025,
expiration date.
DATES: Authority for the Patient
Engagement Advisory Committee would
have expired on October 6, 2025, unless
the Commissioner had formally
determined that renewal is in the public
interest.
FOR FURTHER INFORMATION CONTACT:
Letise Williams, Office of the Center
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
16:32 Nov 01, 2023
Jkt 262001
Director, Center for Devices and
Radiological Health, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 66, Rm. 5407, Silver Spring,
MD 20993–0002, 301–796–8398,
Letise.Williams@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Pursuant
to 41 CFR 102–3.65 and approval by the
Department of Health and Human
Services and by the General Services
Administration, FDA is announcing the
renewal of the Patient Engagement
Advisory Committee (the Committee).
The Committee is a discretionary
Federal advisory committee established
to provide advice to the Commissioner.
The Patient Engagement Advisory
Committee advises the Commissioner or
designee in discharging responsibilities
as they relate to helping to ensure safe
and effective devices for human use
and, as required, any other product for
which FDA has regulatory
responsibility.
The Committee provides advice to the
Commissioner of Food and Drugs or
designee on complex scientific, issues
relating to medical devices, the
regulation of devices, and their use by
patients. Agency guidance and policies,
clinical trial or registry design, patient
preference study design, benefit-risk
determinations, device labeling, unmet
clinical needs, available alternatives,
patient reported outcomes, and devicerelated quality of life measures or health
status issues are among the topics that
may be considered by the Committee.
The Committee provides relevant skills
and perspectives to improve
communication of benefits, risks, and
clinical outcomes, and increase
integration of patient perspectives into
the regulatory process for medical
devices. It performs its duties by
identifying new approaches, promoting
innovation, recognizing unforeseen risks
or barriers, and identifying unintended
consequences that could result from
FDA policy.
Pursuant to its Charter, the Committee
shall consist of a core of nine voting
members, including the Chair. Members
and the Chair are selected by the
Commissioner or designee from among
authorities who are knowledgeable in
areas such as clinical research, patient
experience, and healthcare needs of
patient groups in the United States, or
who are experienced in the work of
patient and health professional
organizations, methodologies for patient
reported outcomes and eliciting patient
preferences, and strategies for
communicating benefits, risks, and
clinical outcomes to patients and
research subjects, as well as other
relevant areas. Members will be invited
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to serve for overlapping terms of up to
4 years. Non-Federal members of this
committee will serve as either as Special
Government Employees or non-voting
representatives. Federal members will
serve as Regular Government
Employees. The core of voting members
may include one technically qualified
member, selected by the Commissioner
or designee, who serves as an
individual, but who is identified with
consumer interests and is recommended
by either a consortium of consumeroriented organizations or other
interested persons. The Commissioner
or designee shall also have the authority
to select from a group of individuals
nominated by industry to serve
temporarily as nonvoting members who
are identified with industry interests.
The number of temporary members
selected for a particular meeting will
depend on the meeting topic.
The Commissioner or designee shall
also have the authority to select
members of other scientific and
technical FDA advisory committees
(normally not to exceed 10 members) to
serve temporarily as voting members
and to designate consultants to serve
temporarily as voting members when:
(1) expertise is required that is not
available among current voting standing
members of the Committee (when
additional voting members are added to
the Committee to provide needed
expertise, a quorum will be based on the
combined total of regular and added
members); or (2) to comprise a quorum
when, because of unforeseen
circumstances, a quorum is or will be
lacking. Because of the size of the
Committee and the variety in the types
of issues that it will consider, FDA may,
in connection with a particular
committee meeting, specify a quorum
that is less than a majority of the current
voting members. The Agency’s
regulations (21 CFR 14.22(d)) authorize
a committee charter to specify quorum
requirements.
Further information regarding the
most recent charter and other
information can be found at https://
www.fda.gov/advisory-committees/
committees-and-meeting-materials/
patient-engagement-advisory-committee
or by contacting the Designated Federal
Officer (see FOR FURTHER INFORMATION
CONTACT). In light of the fact that no
change has been made to the committee
name or description of duties, no
amendment will be made to 21 CFR
14.100.
This notice is issued under the
Federal Advisory Committee Act (5
U.S.C. app.). For general information
related to FDA advisory committees,
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Agencies
[Federal Register Volume 88, Number 211 (Thursday, November 2, 2023)]
[Notices]
[Pages 75289-75290]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-24185]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; State Plan for Grants
to States for Refugee Resettlement (Office of Management and Budget
#0970-0351)
AGENCY: Office of Refugee Resettlement, Administration for Children and
Families, U.S. Department of Health and Human Services.
ACTION: Request for public comments.
-----------------------------------------------------------------------
SUMMARY: The Administration for Children and Families (ACF), Office of
Refugee Resettlement (ORR) is requesting a 3-year extension of the
State Plan for Grants to States for Refugee Resettlement (Office of
Management and Budget #0970-0351, expiration 6/30/2024). ORR is
proposing changes to the form.
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: A State Plan is a required comprehensive narrative
description of the nature and scope of a state's or Replacement
Designee's (RD) Refugee Resettlement Program and provides assurances
that the program will be administered in conformity with the specific
requirements stipulated in 45 CFR 400.4-400.9. The State Plan must
include all applicable state or RD procedures, designations, and
certifications for each requirement as well as supporting
documentation. The plan assures ORR that the state or RD is capable of
administering refugee assistance and coordinating employment and other
social services for eligible caseloads in conformity with specific
requirements.
ORR proposes the following changes to the previously approved State
Plan for Grants to States for Refugee Resettlement:
streamlining/formatting multiple sections of the form,
including technical corrections
enhancing requirements for collaboration and engagement and
expanding the non-discrimination aspects
standardizing sections of the template related to health to
reduce burden by clarifying text and removing duplicative parts
streamlining sections related to the unaccompanied children to
reduce burden by providing better options for responses and selections
and by removing unnecessary and confusing text to ensure consistency
regarding assurances
Respondents: State agencies and RDs under 45 CFR 400.301(c)
administering or supervising the administration of programs.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Annual number Average burden
Instrument Total number of of responses hours per Annual burden
respondents per respondent response hours
----------------------------------------------------------------------------------------------------------------
State Plan for Grants to States for Refugee 59 1 18 1,062
Resettlement...............................
----------------------------------------------------------------------------------------------------------------
[[Page 75290]]
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: 8 U.S.C. 1522 of the Immigration and Nationality Act
(the Act) [Title IV, Sec. 412 of the Act] for each state agency
requesting federal funding for refugee resettlement under 8 U.S.C. 524
[Title IV, Sec. 414 of the Act].
Mary Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2023-24185 Filed 11-1-23; 8:45 am]
BILLING CODE 4184-45-P