Agency Information Collection Activities: Submission for OMB Review; Comment Request, 46122-46123 [2024-11676]
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Federal Register / Vol. 89, No. 103 / Tuesday, May 28, 2024 / Notices
experiences and expectations, provide
an early warning of issues with service,
or focus attention on areas where
communication, training or changes in
operations might improve delivery of
products or services. These collections
will allow for ongoing, collaborative and
actionable communications between the
Agency and its customers and
stakeholders. It will also allow feedback
to contribute directly to the
improvement of program management.
The solicitation of feedback will target
areas such as: timeliness,
appropriateness, accuracy of
information, courtesy, efficiency of
service delivery, and resolution of
issues with service delivery. Responses
will be assessed to plan and inform
efforts to improve or maintain the
quality of service offered to the public.
If this information is not collected, vital
feedback from customers and
stakeholders on the Agency’s services
will be unavailable.
CDC will only submit a collection for
approval under this Generic Clearance if
they meet the following conditions:
• The collections are voluntary;
• The collections are low-burden for
respondents (based) on considerations
of total burden hours, total number of
respondents (or burden-hours per
respondent), and are low-cost for both
the respondents and the Federal
Government;
• The collections are
noncontroversial and do not raise issues
of concern to other Federal agencies;
• Any collection is targeted to the
solicitation of opinions from
respondents who have experience with
the program or may have experience
with the program in the near future;
• Personally identifiable information
(PII) is collected only to the extent
necessary and is not retained;
• Information gathered is intended to
be used only internally for general
service improvement and program
management purposes and is not
intended for release outside of the
agency (if released, the agency must
indicate the qualitative nature of the
information);
• Information gathered will not be
used for the purpose of substantially
informing influential policy decisions;
and
• Information gathered will yield
qualitative information (the collections
will not be designed or expected to
yield statistically reliable results or used
as though the results are generalizable to
the population of study).
Feedback collected under CDC
Generic Clearances provides useful
information, but it does not yield data
that can be generalized to the overall
population. This type of Generic
Clearance for qualitative information
will not be used for quantitative
information collections that are
designed to yield reliably actionable
results, such as monitoring trends over
time or documenting program
performance. Such data uses require
more rigorous designs that address: the
target population to which
generalizations will be made, the
sampling frame, the sample design
(including stratification and clustering),
the precision requirements or power
calculations that justify the proposed
sample size, the expected response rate,
methods for assessing potential
nonresponse bias, the protocols for data
collection, and any testing procedures
that were or will be undertaken prior to
fielding the study. Depending on the
degree of influence the results are likely
to have, such collections may still be
eligible for submission for other Generic
Clearance mechanisms that are designed
to yield quantitative results.
As a general matter, information
collections will not result in any new
System of Records containing Privacy
information and will not ask questions
of a sensitive nature, such as sexual
behavior and attitudes, religious beliefs,
and other matters that are commonly
considered private.
CDC requests OMB approval for an
estimated 13,075 annual burden hours.
There is no cost to respondents other
than their time to participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Type of collections
Individuals and Households, Businesses and
Organizations, State, Local or Tribal Government.
Print Surveys .....................................................
Focus Groups ....................................................
Online Surveys ..................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2024–11590 Filed 5–24–24; 8:45 am]
[Document Identifiers: CMS–10882]
Centers for Medicare & Medicaid
Services
BILLING CODE 4163–18–P
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
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AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
SUMMARY:
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50,000
100
1500
Annual
frequency per
response
Hours per
response
1
1
1
15/60
2
15/60
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including the necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of
the estimated burden, ways to enhance
the quality, utility, and clarity of the
information to be collected, and the use
of automated collection techniques or
other forms of information technology to
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28MYN1
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
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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:
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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
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Agencies
[Federal Register Volume 89, Number 103 (Tuesday, May 28, 2024)]
[Notices]
[Pages 46122-46123]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-11676]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-10882]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. 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 or reinstatement of an
existing collection of information, and to allow a second opportunity
for public comment on the notice. Interested persons are invited to
send comments regarding the burden estimate or any other aspect of this
collection of information, including the necessity and utility of the
proposed information collection for the proper performance of the
agency's functions, the accuracy of the estimated burden, ways to
enhance the quality, utility, and clarity of the information to be
collected, and the use of automated collection techniques or other
forms of information technology to
[[Page 46123]]
minimize the information collection burden.
DATES: 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/PRA-Listing
FOR FURTHER INFORMATION CONTACT: William Parham at (410) 786-4669.
SUPPLEMENTARY INFORMATION: 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 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 [email protected].)
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