Agency Information Collection Activities; Submission for OMB Review; Public Comment Request; of the ACL Generic Information Collection for the Administration on Aging Formula Grant Programs OMB Control Number 0985-New, 46123-46125 [2024-11602]
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Federal Register / Vol. 89, No. 103 / Tuesday, May 28, 2024 / Notices
minimize the information collection
burden.
Comments on the collection(s) of
information must be received by the
OMB desk officer by June 27, 2024.
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.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, please access the CMS PRA
website by copying and pasting the
following web address into your web
browser: https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing
DATES:
FOR FURTHER INFORMATION CONTACT:
William Parham at (410) 786–4669.
Under the
Paperwork Reduction Act of 1995 (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. The term ‘‘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 publish a 30-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension or
reinstatement of an existing collection
of information, before submitting the
collection to OMB for approval. To
comply with this requirement, CMS is
publishing this notice that summarizes
the following proposed collection(s) of
information for public comment:
Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: The Medicare
Advantage and Prescription Drug
Programs: Part C and Part D Medicare
Prescription Payment Plan Model
Documents; Use: Sections 1860D–
2(b)(2)(E)(v)(II)–(IV) of the Act state the
requirements for Part D sponsors and
MA organizations in implementing the
program, which include the processes
for outreach to enrollees identified as
likely to benefit, election, and
khammond on DSKJM1Z7X2PROD with NOTICES
SUPPLEMENTARY INFORMATION:
VerDate Sep<11>2014
18:43 May 24, 2024
Jkt 262001
termination. Subsection II states that
any Part D enrollee may elect into the
program prior to (aa) or during (bb) the
plan year. Subsection III details that
PDP sponsors and MA organizations
must have a mechanism in place to
inform enrollees that they are likely to
benefit from electing into the program at
the point of sale (POS). Subsection IV
(aa) states that plans must terminate a
beneficiary’s participation in the
program when the beneficiary fails to
pay the amounts owed under this
program.
CMS has developed the six materials
in the attached package as model
notices in order to provide standardized
and consistent language for potential
and active program participants,
regardless of which Part D plan they
may be enrolled in. CMS will require
Part D plans to disseminate these
notices, as appropriate, to Part D
enrollees to fulfill the requirements of
the Sections 1860D–2(b)(2)(E)(v)(II)–(IV)
of the Act. Form Number: CMS–10882
(OMB control number: 0938-New);
Frequency: Yearly; Affected Public:
Private, Federal Government, Business
or other for profits, Not-for-profits
institutions; Number of Respondents:
1,065; Total Annual Responses: 1,065;
Total Annual Hours: 21,300. (For policy
questions regarding this collection
contact Michael Brown at (872) 287–
1370 or michael.brown3@cms.hhs.gov.)
William N. Parham, III
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–11676 Filed 5–24–24; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Submission for OMB
Review; Public Comment Request; of
the ACL Generic Information
Collection for the Administration on
Aging Formula Grant Programs OMB
Control Number 0985-New
Administration for Community
Living, HHS.
ACTION: Notice.
AGENCY:
The Administration for
Community Living (ACL) is announcing
that the proposed collection of
information listed above has been
submitted to the Office of Management
and Budget (OMB) for review and
clearance as required under the
Paperwork Reduction Act of 1995. This
SUMMARY:
PO 00000
Frm 00069
Fmt 4703
Sfmt 4703
46123
30-day notice collects comments on the
information collection requirements
related to a new information collection
for the ACL Generic Information
Collection (Gen IC) for the
Administration on Aging Formula Grant
Programs.
DATES: Comments on the collection of
information must be submitted
electronically by 11:59 p.m. (ET) or
postmarked by June 27, 2024.
ADDRESSES: Submit written comments
and recommendations for the proposed
information collection within 30 days of
publication of this notice to
www.reginfo.gov/public/do/PRAMain.
Find the information collection by
selecting ‘‘Currently under 30-day
Review—Open for Public Comments’’ or
by using the search function. By mail to
the Office of Information and Regulatory
Affairs, OMB, New Executive Office
Bldg., 725 17th St. NW, rm. 10235,
Washington, DC 20503, Attn: OMB Desk
Officer for ACL.
FOR FURTHER INFORMATION CONTACT:
Adam Mosey (202) 795–7631 or
Adam.Mosey@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, the
Administration for Community Living
(ACL) has submitted the following
proposed collection of information to
OMB for review and clearance. As a unit
of the Administration for Community
Living, the Administration on Aging
(AoA) provides expertise on program
development, advocacy, and initiatives
for older Americans and their caregivers
and families. Working with State
agencies, local agencies, grantees, and
community providers, AoA directs
programs authorized by the Older
Americans Act (OAA), Elder Justice Act
(EJA), and other legislation that
supports older adults. Through these
programs multi-year State Plans and
assurances, and other financial forms
are needed to provide approval and
oversight of grant recipients. ACL is
seeking OMB approval to add a new
Gen IC to ACL’s Paperwork inventory.
This Gen IC will cover ACL/AoA
formula grant programs for State Plans
on Aging and assurances, State Plans on
Adult Protective Services and
assurances, and other financial forms
associated with aging and APS formula
grant management. Adding a Gen IC
will allow for the collection of data
across programmatic and financial
management of the aging and APS
formula grants.
Statutory Background
In 1965, Congress originally passed
the Older Americans Act (OAA) in
response to concerns by policymakers
E:\FR\FM\28MYN1.SGM
28MYN1
46124
Federal Register / Vol. 89, No. 103 / Tuesday, May 28, 2024 / Notices
khammond on DSKJM1Z7X2PROD with NOTICES
about a lack of community social
services for older adults.
The original legislation established
authority for grants to states for
community planning and social
services, research and development
projects, and personnel training in the
field of aging. Changes to the OAA were
made through the Supporting Older
Americans Act of 2020.
This legislation reauthorized the OAA
and its programs from Federal fiscal
year (FFY) 2020 through 2024. The OAA
provides the foundation for the national
aging network, which includes the
Administration on Aging (AoA), State
Units on Aging (SUA), area agencies on
aging (AAA), Tribal organizations,
service providers, and volunteers. SUAs
are an integral part of the network
responsible for developing and
administering a multi-year state plan
that advocates for and aids older
residents, their families, their
caregivers, and, in many States, for
adults with disabilities.
The Elder Justice Act, passed in 2010,
is the first comprehensive legislation to
address the abuse, neglect, and
exploitation of older adults at the
Federal level. The law authorized a
variety of programs and initiatives to
better coordinate Federal responses to
elder abuse, promote elder justice
research and innovation, support Adult
Protective Services systems, and
provide additional protections for
residents of long-term care facilities.
The importance of these services at the
State-level and local-level is
demonstrated by the fact that states
significantly leverage Older Americans
Act (OAA) funds to obtain other funding
for these activities.
The Coronavirus Response and Relief
Supplemental Appropriations Act of
2021 and the American Rescue Plan Act
that are a part of this Gen IC is to
facilitate OAA formula grant
management.
Financial forms provide statutorily
required information regarding each
State’s contribution to programs to
ensure compliance with legislative
requirements, pertinent Federal
regulations, and other applicable
instructions and guidelines issued by
ACL. This information will be used for
Federal oversight of the Aging Programs.
Based on ACL’s extensive experience
working with APS systems and OAA
grantees on their State plans, ACL does
not anticipate a significantly greater
level of detail for the development of
State plans for APS.
OAA and APS grantees are required to
comply with all terms and conditions
contained in Notices of Award (NoA)
issued by ACL. When it is determined
that a grantee is not in compliance with
one or more of these requirements, ACL
may require a grantee to submit to ACL
a plan to come into compliance under
a Corrective Action Plan (CAP), and any
such CAP may require ACL’s prior
written approval, as determined by
ACL. The CAP process is intended to be
collaborative. Under a CAP, a grantee
and ACL will jointly identify progress
milestones and a feasible timeline for
the grantee to come into compliance
with the applicable requirement.
Grantees must make a good faith effort
at achieving full compliance to continue
to have permission from ACL to operate
under a CAP.
provided two years of Federal funding
($188 million in each year) to support,
for the first time, the nationwide APS
formula grant program authorized by the
Elder Justice Act of 2010. That funding
was used by States to expand or develop
a variety of capabilities that were
necessary to meet increased needs due
to the public health pandemic, and
ongoing funding is necessary to
maintain the improved reach and
effectiveness of APS systems beyond the
pandemic.
The FY 2023 Omnibus
Appropriations Bill provided, for the
first time, an annual appropriation of
$15 million to continue providing
Federal formula grants to State APS
programs. This will be the first time
State entities are required to develop
and submit State plans under Section
2042 of the Elder Justice Act, 42 U.S.C.
1397m-1(b). However, States have
developed spending plans for the
formula funding received to date,
consistent with 45 CFR 75.206(d), and
to update those every three to five years.
This new Gen IC is for programmatic
and financial management of the Aging
and APS formula grants. The purpose of
the State Plans is to document and
provide the opportunity for public
comment on achievements and planned
activities for the multi-year plan period.
A wide range of constituents use or
will use the State Plans to coordinate,
monitor, evaluate, and improve Aging
Network and APS support services by
using the State Plans as a blueprint for
service planning and delivery.
Additionally, ACL leverages State Plans
to understand the numerous services
older adults use, and to utilize the
information for advocating for the needs
of older adults and those who use APS
and for requesting additional funding.
The purpose of the other financial forms
Comments in Response to the 60-Day
Federal Register Notice
A 60-day notice published in the
Federal Register on October 18, 2023, at
88 FR 71869–71871. ACL received one
public comment.
Organization
Section
Comment
Response
Commonwealth of Virginia, Department for Aging and Rehabilitative Services.
Estimated Annualized Burden
Table.
Noted that the burden estimates for State
Plans on Aging, and State Plans on APS
are too low. Recommended identification of
ways to reduce reporting requirements, as
well as revising burden estimates. Recommended survey of states to inform future burden estimates..
ACL appreciates the comment
but declines to make
changes at this time.
Estimated Program Burden: ACL
estimates the burden of this collection
of information as follows:
ESTIMATED ANNUALIZED BURDEN TABLE
Number of
respondents
Respondent/data collection activity
Form
State Unit on Aging (SUA) ................................
State Unit on Aging (SUA) ................................
State Plan on Aging ..........................................
Financial Forms ................................................
VerDate Sep<11>2014
18:43 May 24, 2024
Jkt 262001
PO 00000
Frm 00070
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
14.7
56
E:\FR\FM\28MYN1.SGM
1
5
28MYN1
Average
burden hours
per response
80
1
Total burden
hours
1,176
280
46125
Federal Register / Vol. 89, No. 103 / Tuesday, May 28, 2024 / Notices
ESTIMATED ANNUALIZED BURDEN TABLE—Continued
Form
OAA or APS Grantee ........................................
Corrective Action Plan (CAP) ...........................
Total Estimated Burden ..............................
...........................................................................
Dated: May 21, 2024.
Alison Barkoff,
Principal Deputy Administrator for the
Administration for Community Living,
performing the delegable duties of the
Administrator and the Assistant Secretary for
Aging.
[FR Doc. 2024–11602 Filed 5–24–24; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2023–N–0201]
Jessica Palacio; Denial of Hearing;
Final Debarment Order
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
denying a request for a hearing
submitted by Andrew S. Feldman, on
behalf of Jessica Palacio (Palacio), and is
issuing an order under the Federal
Food, Drug, and Cosmetic Act (FD&C
Act) permanently debarring Palacio
from providing services in any capacity
to a person that has an approved or
pending drug product application. FDA
bases this order on a finding that Palacio
was convicted of a felony under Federal
law for conduct relating to the
development or approval, including the
process for development or approval, of
any drug product under the FD&C Act.
FDA provided notice to Palacio of the
proposed debarment and an opportunity
to request a hearing within the
timeframe prescribed by regulation.
Palacio submitted a request for hearing
but failed to file with the Agency
information and analyses sufficient to
create a basis for a hearing.
DATES: The order is applicable May 28,
2024.
ADDRESSES: Any application for
termination of debarment by Palacio
under section 306(d) of the FD&C Act
(21 U.S.C. 335a(d)) (application) may be
submitted as follows:
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
Electronic Submissions
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
VerDate Sep<11>2014
18:43 May 24, 2024
Jkt 262001
75
I
........................
instructions for submitting comments.
An application submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
application will be made public, you are
solely responsible for ensuring that your
application 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
application, that information will be
posted on https://www.regulations.gov.
• If you want to submit an
application with confidential
information that you do not wish to be
made available to the public, submit the
application 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 a written/paper application
submitted to the Dockets Management
Staff, FDA will post your application, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All applications must
include the Docket No. FDA–2023–N–
0201. An application will be placed in
the docket and, unless 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 an application with confidential
information that you do not wish to be
made publicly available, submit your
application only as a written/paper
submission. You should submit two
copies total. One copy will include the
PO 00000
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Fmt 4703
Number of
responses per
respondent
Number of
respondents
Respondent/data collection activity
Sfmt 4703
Average
burden hours
per response
1
I
........................
Total burden
hours
8
I
........................
600
I
2,056
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 your application.
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 application 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, 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 between 9 a.m.
and 4 p.m., Monday through Friday,
240–402–7500. Publicly available
submissions may be seen in the docket.
FOR FURTHER INFORMATION CONTACT:
Karen Fikes, Office of Scientific
Integrity, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 1, Rm. 4232, Silver Spring,
MD 20993, 301–796–9603.
SUPPLEMENTARY INFORMATION:
I. Background
Section 306(a)(2)(A) of the FD&C Act
mandates permanent debarment if FDA
finds that the individual has been
convicted of a felony under Federal law
for conduct relating to the development
or approval, including the process for
development or approval, of any drug
product. On January 12, 2023, following
a jury trial, the U.S. District Court for
the Southern District of Florida entered
E:\FR\FM\28MYN1.SGM
28MYN1
]]>Agencies
[Federal Register Volume 89, Number 103 (Tuesday, May 28, 2024)]
[Notices]
[Pages 46123-46125]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-11602]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities; Submission for OMB
Review; Public Comment Request; of the ACL Generic Information
Collection for the Administration on Aging Formula Grant Programs OMB
Control Number 0985-New
AGENCY: Administration for Community Living, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Administration for Community Living (ACL) is announcing
that the proposed collection of information listed above has been
submitted to the Office of Management and Budget (OMB) for review and
clearance as required under the Paperwork Reduction Act of 1995. This
30-day notice collects comments on the information collection
requirements related to a new information collection for the ACL
Generic Information Collection (Gen IC) for the Administration on Aging
Formula Grant Programs.
DATES: Comments on the collection of information must be submitted
electronically by 11:59 p.m. (ET) or postmarked by June 27, 2024.
ADDRESSES: Submit written comments and recommendations for the proposed
information collection within 30 days of publication of this notice to
www.reginfo.gov/public/do/PRAMain. Find the information collection by
selecting ``Currently under 30-day Review--Open for Public Comments''
or by using the search function. By mail to the Office of Information
and Regulatory Affairs, OMB, New Executive Office Bldg., 725 17th St.
NW, rm. 10235, Washington, DC 20503, Attn: OMB Desk Officer for ACL.
FOR FURTHER INFORMATION CONTACT: Adam Mosey (202) 795-7631 or
[email protected].
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, the
Administration for Community Living (ACL) has submitted the following
proposed collection of information to OMB for review and clearance. As
a unit of the Administration for Community Living, the Administration
on Aging (AoA) provides expertise on program development, advocacy, and
initiatives for older Americans and their caregivers and families.
Working with State agencies, local agencies, grantees, and community
providers, AoA directs programs authorized by the Older Americans Act
(OAA), Elder Justice Act (EJA), and other legislation that supports
older adults. Through these programs multi-year State Plans and
assurances, and other financial forms are needed to provide approval
and oversight of grant recipients. ACL is seeking OMB approval to add a
new Gen IC to ACL's Paperwork inventory. This Gen IC will cover ACL/AoA
formula grant programs for State Plans on Aging and assurances, State
Plans on Adult Protective Services and assurances, and other financial
forms associated with aging and APS formula grant management. Adding a
Gen IC will allow for the collection of data across programmatic and
financial management of the aging and APS formula grants.
Statutory Background
In 1965, Congress originally passed the Older Americans Act (OAA)
in response to concerns by policymakers
[[Page 46124]]
about a lack of community social services for older adults.
The original legislation established authority for grants to states
for community planning and social services, research and development
projects, and personnel training in the field of aging. Changes to the
OAA were made through the Supporting Older Americans Act of 2020.
This legislation reauthorized the OAA and its programs from Federal
fiscal year (FFY) 2020 through 2024. The OAA provides the foundation
for the national aging network, which includes the Administration on
Aging (AoA), State Units on Aging (SUA), area agencies on aging (AAA),
Tribal organizations, service providers, and volunteers. SUAs are an
integral part of the network responsible for developing and
administering a multi-year state plan that advocates for and aids older
residents, their families, their caregivers, and, in many States, for
adults with disabilities.
The Elder Justice Act, passed in 2010, is the first comprehensive
legislation to address the abuse, neglect, and exploitation of older
adults at the Federal level. The law authorized a variety of programs
and initiatives to better coordinate Federal responses to elder abuse,
promote elder justice research and innovation, support Adult Protective
Services systems, and provide additional protections for residents of
long-term care facilities. The importance of these services at the
State-level and local-level is demonstrated by the fact that states
significantly leverage Older Americans Act (OAA) funds to obtain other
funding for these activities.
The Coronavirus Response and Relief Supplemental Appropriations Act
of 2021 and the American Rescue Plan Act provided two years of Federal
funding ($188 million in each year) to support, for the first time, the
nationwide APS formula grant program authorized by the Elder Justice
Act of 2010. That funding was used by States to expand or develop a
variety of capabilities that were necessary to meet increased needs due
to the public health pandemic, and ongoing funding is necessary to
maintain the improved reach and effectiveness of APS systems beyond the
pandemic.
The FY 2023 Omnibus Appropriations Bill provided, for the first
time, an annual appropriation of $15 million to continue providing
Federal formula grants to State APS programs. This will be the first
time State entities are required to develop and submit State plans
under Section 2042 of the Elder Justice Act, 42 U.S.C. 1397m-1(b).
However, States have developed spending plans for the formula funding
received to date, consistent with 45 CFR 75.206(d), and to update those
every three to five years.
This new Gen IC is for programmatic and financial management of the
Aging and APS formula grants. The purpose of the State Plans is to
document and provide the opportunity for public comment on achievements
and planned activities for the multi-year plan period.
A wide range of constituents use or will use the State Plans to
coordinate, monitor, evaluate, and improve Aging Network and APS
support services by using the State Plans as a blueprint for service
planning and delivery. Additionally, ACL leverages State Plans to
understand the numerous services older adults use, and to utilize the
information for advocating for the needs of older adults and those who
use APS and for requesting additional funding. The purpose of the other
financial forms that are a part of this Gen IC is to facilitate OAA
formula grant management.
Financial forms provide statutorily required information regarding
each State's contribution to programs to ensure compliance with
legislative requirements, pertinent Federal regulations, and other
applicable instructions and guidelines issued by ACL. This information
will be used for Federal oversight of the Aging Programs.
Based on ACL's extensive experience working with APS systems and
OAA grantees on their State plans, ACL does not anticipate a
significantly greater level of detail for the development of State
plans for APS.
OAA and APS grantees are required to comply with all terms and
conditions contained in Notices of Award (NoA) issued by ACL. When it
is determined that a grantee is not in compliance with one or more of
these requirements, ACL may require a grantee to submit to ACL a plan
to come into compliance under a Corrective Action Plan (CAP), and any
such CAP may require ACL's prior written approval, as determined by
ACL. The CAP process is intended to be collaborative. Under a CAP, a
grantee and ACL will jointly identify progress milestones and a
feasible timeline for the grantee to come into compliance with the
applicable requirement. Grantees must make a good faith effort at
achieving full compliance to continue to have permission from ACL to
operate under a CAP.
Comments in Response to the 60-Day Federal Register Notice
A 60-day notice published in the Federal Register on October 18,
2023, at 88 FR 71869-71871. ACL received one public comment.
----------------------------------------------------------------------------------------------------------------
Organization Section Comment Response
----------------------------------------------------------------------------------------------------------------
Commonwealth of Virginia, Department Estimated Annualized Noted that the burden ACL appreciates the
for Aging and Rehabilitative Burden Table. estimates for State comment but declines
Services. Plans on Aging, and to make changes at
State Plans on APS are this time.
too low. Recommended
identification of ways
to reduce reporting
requirements, as well
as revising burden
estimates. Recommended
survey of states to
inform future burden
estimates..
----------------------------------------------------------------------------------------------------------------
Estimated Program Burden: ACL estimates the burden of this
collection of information as follows:
Estimated Annualized Burden Table
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Respondent/data collection Form Number of responses per hours per Total burden
activity respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
State Unit on Aging (SUA)..... State Plan on 14.7 1 80 1,176
Aging.
State Unit on Aging (SUA)..... Financial Forms. 56 5 1 280
[[Page 46125]]
OAA or APS Grantee............ Corrective 75 1 8 600
Action Plan
(CAP).
---------------------------------------------------------------------------------
Total Estimated Burden.... ................ .............. .............. .............. 2,056
----------------------------------------------------------------------------------------------------------------
Dated: May 21, 2024.
Alison Barkoff,
Principal Deputy Administrator for the Administration for Community
Living, performing the delegable duties of the Administrator and the
Assistant Secretary for Aging.
[FR Doc. 2024-11602 Filed 5-24-24; 8:45 am]
BILLING CODE 4154-01-P
