Submission for Office of Management and Budget Review; Guidance for Tribal Temporary Assistance for Needy Families Program (Office of Management and Budget #0970-0157), 45219-45220 [2023-15001]
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Federal Register / Vol. 88, No. 134 / Friday, July 14, 2023 / Notices
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CMS–116 Clinical Laboratory
Improvement Amendments (CLIA)
Application Form and Supporting
Regulations
CMS–2746 End Stage Renal Disease
Death Notification
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 Collection
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Clinical
Laboratory Improvement Amendments
(CLIA) Application Form and
Supporting Regulations; Use: Section
353 (b) of the Public Health Service Act
specifies that the laboratory must
submit an application in such form and
manner as the Secretary shall prescribe
that describes the characteristics of the
laboratory and examinations and
procedures performed by the laboratory.
The application must be completed by
entities performing laboratory’s testing
specimens for diagnostic or treatment
purposes. This information is vital to
the certification process. In this
revision, the majority of changes were
minor changes to the form and
accompanying instructions to facilitate
the completion and data entry of the
form. We anticipate that the changes
will not increase the time to complete
the form. Form Number: CMS–116
(OMB control number: 0938–0581);
Frequency: Biennially and Occasionally;
Affected Public: Private Sector—
Business or other for-profits and Notfor-profit institutions; Number of
Respondents: 64,598; Total Annual
Responses: 64,598; Total Annual Hours:
64,598. (For policy questions regarding
this collection contact Kimberly Weaver
at 410–786–3366.)
2. Type of Information Collection
Request: Reinstatement of a previously
approved collection; Title of
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Information Collection: End Stage Renal
Disease Death Notification; Use: The
ESRD Death Notification form (CMS–
2746) is completed by all Medicareapproved ESRD facilities upon death of
an ESRD patient. Its primary purpose is
to collect fact of death and cause of
death of ESRD patients. The ESRD
Program Management and Medical
Information System (PMMIS) has the
responsibility of collecting, maintaining,
and disseminating, on a national basis,
uniform data pertaining to ESRD
patients and their treatment of care. All
renal facilities approved to participate
in the ESRD program are required by
Public Law 95–292 to supply data to
this system.
Federal regulations require that the
ESRD Networks examine the mortality
rates of every Medicare-approved
facility within its area of responsibility.
CMS–2746 provides the necessary data
to assist the ESRD Networks in making
decisions that result in improved
patient care and in cost-effective
distribution of ESRD resources. The data
is used by the ESRD Networks to verify
facility deaths and to monitor facility
performance. The form is also used by
health care planning agencies and
researchers to determine survival rates
by diagnoses. This request is to revise
the form to better align with the
common verbiage used on standardized
forms, by other Federal agencies,
including the Census Bureau. Form
Number: CMS–2746 (OMB control
number: 0938–0448); Frequency: Yearly;
Affected Public: Private Sector (Business
or other for-profits, Not-for-Profit
Institutions); Number of Respondents:
7,726; Total Annual Responses:
101,491; Total Annual Hours: 50,746.
(For policy questions regarding this
collection contact Christina Goatee at
410–786–6689.)
Dated: July 11, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2023–14985 Filed 7–13–23; 8:45 am]
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45219
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10847]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Correction
In notice document 2023–14176
beginning on page 42722 in the issue of
Monday, July 3, 2023, make the
following correction:
On page 42722, in the third column,
in the third line of the DATES section,
‘‘August 2, 2023’’ should read ‘‘July 31,
2023’’.
[FR Doc. C1–2023–14176 Filed 7–13–23; 8:45 am]
BILLING CODE 0099–10–D
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for Office of Management
and Budget Review; Guidance for
Tribal Temporary Assistance for Needy
Families Program (Office of
Management and Budget #0970–0157)
Office of Family Assistance;
Administration for Children and
Families; Department of Health and
Human Services.
ACTION: Request for public comment.
AGENCY:
The Administration for
Children and Families (ACF) is
requesting a 3-year extension of the
form ACF–123: Guidance for the Tribal
Temporary Assistance for Needy
Families (TANF) Program (Office of
Management and Budget (OMB) #0970–
0157, expiration date: August 31, 2023).
There are minor clarifying changes
requested to the guidance.
DATES: Comments due within 30 days of
publication. OMB is required to make a
decision concerning 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
SUMMARY:
E:\FR\FM\14JYN1.SGM
14JYN1
45220
Federal Register / Vol. 88, No. 134 / Friday, July 14, 2023 / Notices
for Public Comments’’ or by using the
search function.
SUPPLEMENTARY INFORMATION:
Description: 42 U.S.C. 612 (Section
412 of the Social Security Act) requires
each Indian tribe that elects to
administer and operate a TANF program
to submit a TANF Tribal Plan. This
request includes the renewal of the
guidance for completing the initial
Tribal TANF Plan. The TANF Tribal
Plan is a mandatory statement
submitted to the Secretary of the United
States Department of Health and Human
Services (HHS) by the Indian tribe,
which consists of an outline of how the
Indian tribe’s TANF program will be
administered and operated. It is used by
the Secretary to determine whether the
plan is approvable and to determine that
the Indian tribe is eligible to receive a
TANF assistance grant. It is also made
available to the public. The renewal
includes minor edits, such as updating
hyperlinks and correcting typographical
errors. Additionally, the list of
requirements has been reformatted so
that it is easier to read and use.
Respondents: Indian tribes applying
to operate a TANF program and to
renew their Tribal Family Assistance
Plan.
ANNUAL BURDEN ESTIMATES
Instrument
Total number
of respondents
Total number
of responses
per
respondent
Average
burden hours
per response
Total burden
hours
Annual burden
hours
Guidance for the TANF Program .........................................
75
1
68
5,100
1,700
Estimated Total Annual Burden
Hours: 1,700.
Authority: 42 U.S.C. 612.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2023–15001 Filed 7–13–23; 8:45 am]
BILLING CODE 4184–36–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2023–N–2680]
Pediatric Advisory Committee; Notice
of Meeting; Establishment of a Public
Docket; Request for Comments
AGENCY:
Food and Drug Administration,
HHS.
Notice; establishment of a
public docket; request for comments.
ACTION:
The Food and Drug
Administration (FDA or the Agency)
announces a forthcoming public
advisory committee meeting of the
Pediatric Advisory Committee (the
Committee). The general function of the
Committee is to provide advice and
recommendations to the Agency on
pediatric regulatory issues. At least one
portion of the meeting will be closed to
the public. FDA is establishing a docket
for public comment on this document.
DATES: The meeting will be held
virtually on September 19, 2023, from 9
a.m. to 5:30 p.m. Eastern Time and
September 20, 2023, from 9 a.m. to 1
p.m. Eastern Time.
ADDRESSES: All meeting participants
will be joining this advisory committee
via an online teleconferencing platform.
All meeting participants will be heard,
viewed, captioned, and recorded for this
advisory committee meeting via an
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SUMMARY:
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online teleconferencing and/or video
conferencing platform. Answers to
commonly asked questions about FDA
advisory committee meetings may be
accessed at: https://www.fda.gov/
AdvisoryCommittees/
AboutAdvisoryCommittees/ucm408555.
htm.
FDA is establishing a docket for
public comment on this meeting. The
docket number is FDA–2023–N–2680.
The docket will close on September 18,
2023. 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 September 18, 2023.
Comments received by mail/hand
delivery/courier (for written/paper
submissions) will be considered timely
if they are received on or before that
date.
Comments received on or before
September 5, 2023, will be provided to
the Committee. Comments received after
that date will be taken into
consideration by FDA. In the event that
the meeting is cancelled, FDA will
continue to evaluate any relevant
applications or information, and
consider any comments submitted to the
docket, as appropriate.
You may submit comments as
follows:
Electronic Submissions
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
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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.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment 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 written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2023–N–2680 for ‘‘Pediatric Advisory
Committee; Notice of Meeting;
Establishment of a Public Docket;
Request for Comments.’’ Received
comments, those filed in a timely
manner (see ADDRESSES), will be placed
in the docket and, except for those
submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
Dockets Management Staff between 9
E:\FR\FM\14JYN1.SGM
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Agencies
[Federal Register Volume 88, Number 134 (Friday, July 14, 2023)]
[Notices]
[Pages 45219-45220]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-15001]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for Office of Management and Budget Review; Guidance
for Tribal Temporary Assistance for Needy Families Program (Office of
Management and Budget #0970-0157)
AGENCY: Office of Family Assistance; Administration for Children and
Families; Department of Health and Human Services.
ACTION: Request for public comment.
-----------------------------------------------------------------------
SUMMARY: The Administration for Children and Families (ACF) is
requesting a 3-year extension of the form ACF-123: Guidance for the
Tribal Temporary Assistance for Needy Families (TANF) Program (Office
of Management and Budget (OMB) #0970-0157, expiration date: August 31,
2023). There are minor clarifying changes requested to the guidance.
DATES: Comments due within 30 days of publication. OMB is required to
make a decision concerning 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
[[Page 45220]]
for Public Comments'' or by using the search function.
SUPPLEMENTARY INFORMATION:
Description: 42 U.S.C. 612 (Section 412 of the Social Security Act)
requires each Indian tribe that elects to administer and operate a TANF
program to submit a TANF Tribal Plan. This request includes the renewal
of the guidance for completing the initial Tribal TANF Plan. The TANF
Tribal Plan is a mandatory statement submitted to the Secretary of the
United States Department of Health and Human Services (HHS) by the
Indian tribe, which consists of an outline of how the Indian tribe's
TANF program will be administered and operated. It is used by the
Secretary to determine whether the plan is approvable and to determine
that the Indian tribe is eligible to receive a TANF assistance grant.
It is also made available to the public. The renewal includes minor
edits, such as updating hyperlinks and correcting typographical errors.
Additionally, the list of requirements has been reformatted so that it
is easier to read and use.
Respondents: Indian tribes applying to operate a TANF program and
to renew their Tribal Family Assistance Plan.
Annual Burden Estimates
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total number of Average burden
Instrument Total number of responses per hours per Total burden Annual burden
respondents respondent response hours hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Guidance for the TANF Program...................................... 75 1 68 5,100 1,700
--------------------------------------------------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 1,700.
Authority: 42 U.S.C. 612.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2023-15001 Filed 7-13-23; 8:45 am]
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