14-Day FRN - ACF-696T Updates Sept 2024

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Federal Register / Vol. 89, No. 172 / Thursday, September 5, 2024 / Notices

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10902]

Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
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
(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
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates 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 minimize the
information collection burden.
DATES: Comments must be received by
November 4, 2024.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to http://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number: lll, Room C4–26–
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.

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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.
FOR FURTHER INFORMATION CONTACT:
William N. Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10902 Environmental Health
Hazards Checklist Medicare Coverage
for Individuals Exposed to
Environmental Health Hazards
Under the 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
requires Federal agencies to publish a
60-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.
Information Collections
1. Type of Information Collection
Request: New Collection (Request for a
new OMB control number); Title of
Information Collection: Environmental
Health Hazards Checklist Medicare
Coverage for Individuals Exposed to
Environmental Health Hazards; Use:
Section 1881A of the Act provides an
enrollment basis for individuals who
have been exposed to environmental
health hazards. Currently, the only
individuals eligible for Medicare under
this provision are those who were
present in Lincoln County, Montana,
and have an asbestos-related disease
(ARD) diagnosis. Eligible individuals
must be diagnosed with one or more
asbestos-related conditions and have

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been present in Lincoln County,
Montana, for a total of at least 6 months
(need not be consecutive) in the period
ending 10 years or more before
diagnosis of an asbestos-related
condition. This form provides
verification from a provider so that SSA
can determine eligibility for Medicare
enrollment.
SSA uses this information to
determine whether an individual meets
the requirements for Medicare
enrollment on the basis of an
Environmental Health Hazard. The form
is faxed to the applicant’s provider by
SSA. The provider must complete and
sign the form and submit it back to SSA
via fax or mail. The information on the
completed form is reviewed manually
by SSA. Thus, the collection of this
information does not involve the use of
information technology. Form Number:
CMS–10902 (OMB control number:
0938–New); Frequency: Once; Affected
Public: Individuals and Households;
Number of Respondents: 61; Total
Annual Responses: 61; Total Annual
Hours: 10. (For policy questions
regarding this collection contact Tyrissa
Woods at 410–786–0286 or
[email protected]).
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–19867 Filed 9–4–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Child Care Development Fund
(CCDF) ACF–696T Financial Report for
Tribes (OMB #0970–0510)
Office of Child Care,
Administration for Children and
Families, U.S. Department of Health and
Human Services.
ACTION: Request for public comments.
AGENCY:

The Administration for
Children and Families (ACF) Office of
Child Care plans to submit revisions to
an approved generic information
collection (GenIC) under the umbrella
generic: Generic Clearance for Financial
Reports used for ACF Non-Discretionary
Grant Programs (0970–0510). The
request revises ACF–696T, the annual
financial report for tribal CCDF grant
programs to submit financial claims.
This specific form collects financial data
for Tribal CCDF programs. The

SUMMARY:

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Federal Register / Vol. 89, No. 172 / Thursday, September 5, 2024 / Notices
proposed revisions to the ACF–696T
will provide reporting instructions to
Tribal Lead Agencies who are approved
under a temporary opportunity to
retroactively request the use CCDF
funds, including most COVID-relief
funds, for construction and/or major
renovation with the intent of offsetting
increased costs of materials, labor, and
other related project costs.
DATES: Comments due within 14 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 and below.
ADDRESSES: Copies of the proposed
collection of information can be

obtained and comments may be
forwarded by emailing infocollection@
acf.hhs.gov. All requests should be
identified by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: ACF programs require
detailed financial information from their
grantees that allows ACF to monitor
various specialized cost categories
within each program, to closely manage
program activities, and to have
sufficient financial information to
enable periodic thorough and detailed
audits. Generic Clearance for Financial
Reports used for ACF Non-Discretionary
Grant Programs allows ACF programs to
efficiently develop and receive approval
for financial reports that are tailored to

specific funding recipients and the
associated needs of the program. For
more information about the umbrella
generic, see: https://www.reginfo.gov/
public/do/PRAViewDocument?ref_
nbr=202108-0970-002.
This specific GenIC collects financial
data for tribal CCDF programs. The
proposed revisions to the ACF–696T
will provide reporting instructions to
Tribal Lead Agencies who are approved
under a temporary opportunity to
retroactively request the use CCDF
funds, including most COVID-relief
funds, for construction and/or major
renovation with the intent of offsetting
increased costs of materials, labor, and
other related project costs.

ANNUAL BURDEN ESTIMATES
Number of
respondents

Title of information collection
ACF–696T ............................................................................................................

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 14 days of this publication.
Authority: 42 U.S.C. 9857, 42 U.S.C.
618.
Mary C. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2024–19916 Filed 9–4–24; 8:45 am]

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219

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2024–N–3902]

Agency Information Collection
Activities; Proposed Collection;
Comment Request; Registration of
Producers of Drugs and Listing of
Drugs in Commercial Distribution and
Related Collections of Information
AGENCY:

Food and Drug Administration,

HHS.
ACTION:

Notice.

The Food and Drug
Administration (FDA, the Agency, or
we) is announcing an opportunity for
public comment on the proposed
collection of certain information by the
Agency. 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 of an
existing collection of information, and
to allow 60 days for public comment in
response to the notice. This notice
solicits comments on the information
collections related to requirements for
drug establishment registration and drug
listing, including registrant reporting
under the Federal Food, Drug, and
Cosmetic Act (FD&C Act) with respect
to listed drugs and certain guidances.
DATES: Either electronic or written
comments on the collection of

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Hourly
burden per
response
1

Annual
hourly
burden
5

1,095

information must be submitted by
November 4, 2024.
You may submit comments
as follows. Please note that late,
untimely filed comments will not be
considered. The https://
www.regulations.gov electronic filing
system will accept comments until
11:59 p.m. Eastern Time at the end of
November 4, 2024. Comments received
by mail/hand delivery/courier (for
written/paper submissions) will be
considered timely if they are received
on or before that date.

ADDRESSES:

Electronic Submissions

SUMMARY:

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Annual
frequency of
responses

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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://
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.

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