Agency Information Collection Activities: Submission for OMB Review; Comment Request, 30377-30379 [2024-08658]
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30377
Federal Register / Vol. 89, No. 79 / Tuesday, April 23, 2024 / Notices
aggregate reporting only; not to be
reported for each individual
participant); an OMB-recommended sixpoint disability variable (not tied to CDC
recognition and with a variable option
of ‘Participant chose not to respond’); a
health equity-related social
determinants of health (SDOH) variable
set (to assess whether there was a social
needs assessment conducted; key SDOH
issues identified; and whether any
action was taken; not tied to CDC
recognition); a Middle Eastern or North
African write-in option within the
current race/ethnicity variable; and two
new options for the current payersource
variable.
Key changes to the application data
collection instrument allow for a yes/no
drop-down question asking if an
organization’s zip code is in an area of
high social vulnerability based on the
Social Vulnerability Index, which
would permit an in-person organization
to be fast-tracked to Preliminary
recognition status to allow the
organization to apply to CMS to become
an MDPP supplier; revisions to the
combination delivery mode to include
an option for in-person delivery with a
distance learning component; and
collection of a projected program startdate.
During the period of this Revision,
CDC estimates receipt of approximately
200 DPRP application forms per year
from new organizations. The estimated
burden per one-time application
response is one hour (annualized to 200
hours). In addition, CDC estimates
receipt of semi-annual evaluation data
submissions from the same 200
additional organizations per year,
estimated at two hours per response.
The total estimated average annualized
evaluation burden for new respondents
is 2,400 hours. This includes an
estimate of the time needed to extract
and compile the required data records
and fields from an existing electronic
database, review the data, and enter the
data via the DPRP Data Portal. CDC also
has 1,500 currently recognized
organizations that will continue to
submit semi-annual evaluation data.
These organizations are reflected in
Supporting Statement B within this
OMB revision.
The estimated burden per response is
moderate, since the information
requested for CDC recognition is
routinely collected by most
organizations that deliver the National
DPP lifestyle change program for their
own internal evaluation and possible
insurance reimbursement purposes,
including the MDPP benefit.
Participation in the DPRP is voluntary,
data are de-identified, no personally
identifiable information (PII) is
collected by CDC, and there are no costs
to respondents other than their time.
CDC is requesting a three-year approval.
The total estimated annualized burden
is 7,800 hours.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Public sector organizations that deliver the National DPP
lifestyle change program.
Private sector organizations that deliver the National DPP
lifestyle change program.
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
[FR Doc. 2024–08593 Filed 4–22–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10434]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services.
ACTION: Notice.
ddrumheller on DSK120RN23PROD with NOTICES1
AGENCY:
On May 28, 2010, the Office
of Management and Budget (OMB)
issued Paperwork Reduction Act (PRA)
guidance related to the ‘‘generic’’
clearance process. Generally, this is an
expedited clearance process by which
agencies may obtain OMB’s approval of
SUMMARY:
VerDate Sep<11>2014
17:48 Apr 22, 2024
Jkt 262001
Number of
respondents
Form name
DPRP
DPRP
DPRP
DPRP
Application Form .........
Evaluation Data ..........
Application Form .........
Evaluation Data ..........
collection of information requests that
are ‘‘usually voluntary, low-burden, and
uncontroversial,’’ do not raise any
substantive or policy issues, and do not
require policy or methodological
review. The process requires the
submission of an overarching plan that
defines the scope of the individual
collections that may be submitted under
that umbrella. This notice is intended to
advise the public of our intent to extend
OMB’s approval of our MACPro
(Medicaid and CHIP Program) umbrella
and all of the individual generic
collection of information requests that
fall under that umbrella. This notice
also provides the public with general
instructions for obtaining documents
that are associated with such collections
and for submitting comments.
DATES: Comments must be received by
May 23, 2024.
ADDRESSES:
Submitting Comments: When
commenting, please reference the
applicable collection’s CMS ID number
and/or the OMB control number (both
numbers are listed below under the
SUPPLEMENTARY INFORMATION caption).
To be assured consideration, comments
and recommendations must be
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80
740
120
1,160
Number of
responses per
respondent
1
2
1
2
Avg. burden
per response
(in hours)
1
2
1
2
submitted in any one of the following
ways and by the applicable due date:
1. Electronically. We encourage you to
submit comments through the Federal
eRulemaking portal at the applicable
web address listed below under the
SUPPLEMENTARY INFORMATION caption
under ‘‘Docket Information.’’ If needed,
instructions for submitting such
comments can be found on that website.
2. By regular mail. Alternatively, you
can submit written comments to the
following address:
CMS, Office of Strategic Operations
and Regulatory Affairs (OSORA),
Division of Regulations Development,
Attention: CMS–10434/OMB 0938–
1188, Room C4–26–05, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
Obtaining Documents: To obtain
copies of supporting statements and any
related forms and supporting documents
for the collections listed in this notice,
please refer to the following
instructions:
1. We encourage you to access the
Federal eRulemaking portal at the
applicable web address listed below
under the SUPPLEMENTARY INFORMATION
caption under ‘‘Docket Information.’’ If
needed, follow the online instructions
E:\FR\FM\23APN1.SGM
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30378
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for accessing the applicable docket and
the documents contained therein.
For
general information contact William N.
Parham at 410–786–4669. For policy
related questions, contact the individual
listed below under the SUPPLEMENTARY
INFORMATION caption under ‘‘Docket
Information.’’
FOR FURTHER INFORMATION CONTACT:
Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from
OMB for each collection of information
that they conduct or sponsor. The term
‘‘collection of information’’ is defined in
44 U.S.C. 3502(3) and 5 CFR 1320.3(c).
Generally, it applies to voluntary and
mandatory requirements that are related
to any one or more of the following
activities: the collection of information,
the reporting of information, the
disclose of information to a third-party,
and/or recordkeeping.
While there are some exceptions
(such as collections having nonsubstantive changes and collections
requesting emergency approval) section
3506(c)(2)(A) of the PRA requires
Federal agencies to publish 60- and 30day notices in the Federal Register and
solicit comment on each of its proposed
collections of information, including:
new collections, extensions of existing
collections, revisions of existing
collections, and reinstatements of
previously approved collections before
submitting such collections to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
Interested parties are invited to
submit comments regarding our burden
estimates or any other aspect of the
collection, including: the necessity and
utility of the proposed information
collection for the proper performance of
our agency’s functions; the accuracy of
burden estimates; 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. See DATES and ADDRESSES for
instructions for submitting comments.
While we will review all comments
received, we may choose not to post offtopic or inappropriate comments.
Otherwise, all comments will be posted
without edit under the applicable
docket number, including any personal
information that the commenter
provides. Our response to such
comments will be posted at reginfo.gov
under the applicable OMB control
number.
ddrumheller on DSK120RN23PROD with NOTICES1
SUPPLEMENTARY INFORMATION:
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17:48 Apr 22, 2024
Jkt 262001
Medicaid and CHIP Program (MACPro)
5. Title: Medicaid State Plan Eligibility
At this time, MACPro is made up of
the main umbrella (see collection
number 1 in the following list) and nine
individual generic collections of
information (see collection numbers 2
through 10 in the following list). Details
such as the collection’s requirements
and burden estimates can be found in
the collection’s supporting statement
and associated materials (see ADDRESSES
for instructions for obtaining such
documents).
Type of Request: Extension of a
currently approved collection.
CMS ID Number: CMS–10434 #15.
OMB Control Number: 0938–1188.
eRulemaking Docket ID Number:
CMS–2023–0090.
Docket Web Address: https://
www.regulations.gov/docket/CMS-20230090.
For Policy Related Questions, Contact:
Suzette Seng at 410–786–4703.
Docket Information
1. Title: Medicaid and CHIP Program
(MACPro)
Type of Request: Revision of a
currently approved collection.
CMS ID Number: CMS–10434.
OMB Control Number: 0938–1188.
eRulemaking Docket ID Number:
CMS–2023–0080.
Docket Web Address: https://
www.regulations.gov/docket/CMS-20230080.
For Policy Related Questions, Contact:
William N. Parham at 410–786–4669.
2. Title: Initial Application
Type of Request: Extension of a
currently approved collection.
CMS ID Number: CMS–10434 #1.
OMB Control Number: 0938–1188.
eRulemaking Docket ID Number:
CMS–2023–0081.
Docket Web Address: https://
www.regulations.gov/docket/CMS-20230081.
For Policy Related Questions, Contact:
Stephanie Bell at 410–786–0617.
6. Title: Health Home State Plan
Amendment (SPA)
Type of Request: Extension of a
currently approved collection.
CMS ID Number: CMS–10434 #22.
OMB Control Number: 0938–1188.
eRulemaking Docket ID Number:
CMS–2023–0084.
Docket Web Address: https://
www.regulations.gov/docket/CMS-20230084.
For Policy Related Questions, Contact:
Mary Pat Farkas at 410–786–5731.
7. Title: Medicaid Adult and Child Core
Set Measures
Type of Request: Extension of a
currently approved collection.
CMS ID Number: CMS–10434 #26.
OMB Control Number: 0938–1188.
eRulemaking Docket ID Number:
CMS–2023–0085.
Docket Web Address: https://
www.regulations.gov/docket/CMS-20230085.
For Policy Related Questions, Contact:
Virginia (Gigi) Raney at 410–786–6117.
3. Title: CHIP State Plan Eligibility
8. Title: Maternal and Infant Health
Quality
Type of Request: Extension of a
currently approved collection.
CMS ID Number: CMS–10434 #2.
OMB Control Number: 0938–1188.
eRulemaking Docket ID Number:
CMS–2023–0082.
Docket Web Address: https://
www.regulations.gov/docket/CMS-20230082.
For Policy Related Questions, Contact:
Stephanie Bell at 410–786–0617.
Type of Request: Extension of a
currently approved collection.
CMS ID Number: CMS–10434 #45.
OMB Control Number: 0938–1188.
eRulemaking Docket ID Number:
CMS–2023–0086.
Docket Web Address: https://
www.regulations.gov/docket/CMS-20230086.
For Policy Related Questions, Contact:
Virginia (Gigi) Raney at 410–786–6117.
4. Title: Alternative Benefit Plans (ABPs)
9. Title: Health Home Core Sets
Type of Request: Extension of a
currently approved collection.
CMS ID Number: CMS–10434 #3.
OMB Control Number: 0938–1188.
eRulemaking Docket ID Number:
CMS–2023–0083.
Docket Web Address: https://
www.regulations.gov/docket/CMS-20230083.
For Policy Related Questions, Contact:
Adrienne Delozier at 410–786–0278.
Type of Request: Extension of a
currently approved collection.
CMS ID Number: CMS–10434 #47.
OMB Control Number: 0938–1188.
eRulemaking Docket ID Number:
CMS–2023–0087.
Docket Web Address: https://
www.regulations.gov/docket/CMS-20230087.
For Policy Related Questions, Contact:
Mary Pat Farkas at 410–786–5731.
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Federal Register / Vol. 89, No. 79 / Tuesday, April 23, 2024 / Notices
10. Title: Medicaid Extended
Postpartum Coverage and Continuous
Eligibility for Children
Type of Request: Extension of a
currently approved collection.
CMS ID Number: CMS–10434 #77.
OMB Control Number: 0938–1188.
eRulemaking Docket ID Number:
CMS–2023–0088.
Docket Web Address: https://
www.regulations.gov/docket/CMS-20230088.
For Policy Related Questions, Contact:
Alexa Turner at 410–786–8823.
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–08658 Filed 4–22–24; 8:45 am]
Administration for Children and
Families
Proposed Information Collection
Activity; Community Services Block
Grant (CSBG) Model Tribal Plan and
Application (New Collection)
Office of Community Services,
Administration for Children and
Families, U.S. Department of Health and
Human Services.
AGENCY:
ACTION:
Request for public comments.
The Office of Community
Services (OCS), Administration for
Children and Families (ACF), requests
an approval of the Community Services
Block Grant (CSBG) Model Tribal Plan.
SUMMARY:
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.
DATES:
BILLING CODE 4120–01–P
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: Section 677 of the CSBG
Act requires Indian tribes or tribal
organizations to submit an application
and plan (CSBG Model Tribal Plan). The
CSBG Model Tribal Plan must meet
statutory requirements prior to OCS
awarding CSBG tribal grant recipients
with CSBG funds. Tribal grant
recipients have the option to submit a
detailed plan annually or biannually.
Tribal grant recipients that submit a
biannual plan must provide an
abbreviated plan the following year if
substantial changes to the initial plan
will occur. The CSBG Model Tribal Plan
has been used in previous years without
OMB approval. To come into
compliance with the PRA, ACF is
submitting the CSBG Model Tribal Plan
as a new request to OMB.
Respondents: Tribal grant recipients
(tribes and tribal organizations)
ADDRESSES:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
ANNUAL BURDEN ESTIMATES
Instrument
Total number
of respondents
Annual number
of responses
per respondent
Average
burden hours
per response
Annual
burden
hours
CSBG Model Tribal Plan .........................................................................
66
1
10
660
ddrumheller on DSK120RN23PROD with NOTICES1
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: Sec. 677, Pub. L. 105–285,
112 Stat. 2742 (42 U.S.C. 9911)
Mary C. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2024–08668 Filed 4–22–24; 8:45 am]
BILLING CODE 4184–27–P
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17:48 Apr 22, 2024
Jkt 262001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2024–N–1786]
PAI Holdings, LLC DBA
Pharmaceutical Associates, Inc., et al.;
Withdrawal of Approval of 23 New
Drug Applications
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
withdrawing approval of 23 new drug
applications (NDAs) from multiple
applicants. The applicants notified the
Agency in writing that the drug
products were no longer marketed and
requested that the approval of the
applications be withdrawn.
DATES: Approval is withdrawn as of
May 23, 2024.
SUMMARY:
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Frm 00060
Fmt 4703
Sfmt 4703
FOR FURTHER INFORMATION CONTACT:
Kimberly Lehrfeld, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, Rm. 6226,
Silver Spring, MD 20993–0002, 301–
796–3137, Kimberly.Lehrfeld@
fda.hhs.gov.
The
applicants listed in the table have
informed FDA that these drug products
are no longer marketed and have
requested that FDA withdraw approval
of the applications under the process in
§ 314.150(c) (21 CFR 314.150(c)). The
applicants have also, by their requests,
waived their opportunity for a hearing.
Withdrawal of approval of an
application or abbreviated application
under § 314.150(c) is without prejudice
to refiling.
SUPPLEMENTARY INFORMATION:
E:\FR\FM\23APN1.SGM
23APN1
Agencies
[Federal Register Volume 89, Number 79 (Tuesday, April 23, 2024)]
[Notices]
[Pages 30377-30379]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-08658]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10434]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, Health and Human
Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: On May 28, 2010, the Office of Management and Budget (OMB)
issued Paperwork Reduction Act (PRA) guidance related to the
``generic'' clearance process. Generally, this is an expedited
clearance process by which agencies may obtain OMB's approval of
collection of information requests that are ``usually voluntary, low-
burden, and uncontroversial,'' do not raise any substantive or policy
issues, and do not require policy or methodological review. The process
requires the submission of an overarching plan that defines the scope
of the individual collections that may be submitted under that
umbrella. This notice is intended to advise the public of our intent to
extend OMB's approval of our MACPro (Medicaid and CHIP Program)
umbrella and all of the individual generic collection of information
requests that fall under that umbrella. This notice also provides the
public with general instructions for obtaining documents that are
associated with such collections and for submitting comments.
DATES: Comments must be received by May 23, 2024.
ADDRESSES:
Submitting Comments: When commenting, please reference the
applicable collection's CMS ID number and/or the OMB control number
(both numbers are listed below under the SUPPLEMENTARY INFORMATION
caption). To be assured consideration, comments and recommendations
must be submitted in any one of the following ways and by the
applicable due date:
1. Electronically. We encourage you to submit comments through the
Federal eRulemaking portal at the applicable web address listed below
under the SUPPLEMENTARY INFORMATION caption under ``Docket
Information.'' If needed, instructions for submitting such comments can
be found on that website.
2. By regular mail. Alternatively, you can submit written comments
to the following address:
CMS, Office of Strategic Operations and Regulatory Affairs (OSORA),
Division of Regulations Development, Attention: CMS-10434/OMB 0938-
1188, Room C4-26-05, 7500 Security Boulevard, Baltimore, MD 21244-1850.
Obtaining Documents: To obtain copies of supporting statements and
any related forms and supporting documents for the collections listed
in this notice, please refer to the following instructions:
1. We encourage you to access the Federal eRulemaking portal at the
applicable web address listed below under the SUPPLEMENTARY INFORMATION
caption under ``Docket Information.'' If needed, follow the online
instructions
[[Page 30378]]
for accessing the applicable docket and the documents contained
therein.
FOR FURTHER INFORMATION CONTACT: For general information contact
William N. Parham at 410-786-4669. For policy related questions,
contact the individual listed below under the SUPPLEMENTARY INFORMATION
caption under ``Docket Information.''
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3520), Federal
agencies must obtain approval from OMB for each collection of
information that they conduct or sponsor. The term ``collection of
information'' is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c).
Generally, it applies to voluntary and mandatory requirements that are
related to any one or more of the following activities: the collection
of information, the reporting of information, the disclose of
information to a third-party, and/or recordkeeping.
While there are some exceptions (such as collections having non-
substantive changes and collections requesting emergency approval)
section 3506(c)(2)(A) of the PRA requires Federal agencies to publish
60- and 30-day notices in the Federal Register and solicit comment on
each of its proposed collections of information, including: new
collections, extensions of existing collections, revisions of existing
collections, and reinstatements of previously approved collections
before submitting such collections to OMB for approval. To comply with
this requirement, CMS is publishing this notice.
Interested parties are invited to submit comments regarding our
burden estimates or any other aspect of the collection, including: the
necessity and utility of the proposed information collection for the
proper performance of our agency's functions; the accuracy of burden
estimates; 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. See DATES and ADDRESSES for instructions
for submitting comments.
While we will review all comments received, we may choose not to
post off-topic or inappropriate comments. Otherwise, all comments will
be posted without edit under the applicable docket number, including
any personal information that the commenter provides. Our response to
such comments will be posted at reginfo.gov under the applicable OMB
control number.
Medicaid and CHIP Program (MACPro)
At this time, MACPro is made up of the main umbrella (see
collection number 1 in the following list) and nine individual generic
collections of information (see collection numbers 2 through 10 in the
following list). Details such as the collection's requirements and
burden estimates can be found in the collection's supporting statement
and associated materials (see ADDRESSES for instructions for obtaining
such documents).
Docket Information
1. Title: Medicaid and CHIP Program (MACPro)
Type of Request: Revision of a currently approved collection.
CMS ID Number: CMS-10434.
OMB Control Number: 0938-1188.
eRulemaking Docket ID Number: CMS-2023-0080.
Docket Web Address: https://www.regulations.gov/docket/CMS-2023-0080.
For Policy Related Questions, Contact: William N. Parham at 410-
786-4669.
2. Title: Initial Application
Type of Request: Extension of a currently approved collection.
CMS ID Number: CMS-10434 #1.
OMB Control Number: 0938-1188.
eRulemaking Docket ID Number: CMS-2023-0081.
Docket Web Address: https://www.regulations.gov/docket/CMS-2023-0081.
For Policy Related Questions, Contact: Stephanie Bell at 410-786-
0617.
3. Title: CHIP State Plan Eligibility
Type of Request: Extension of a currently approved collection.
CMS ID Number: CMS-10434 #2.
OMB Control Number: 0938-1188.
eRulemaking Docket ID Number: CMS-2023-0082.
Docket Web Address: https://www.regulations.gov/docket/CMS-2023-0082.
For Policy Related Questions, Contact: Stephanie Bell at 410-786-
0617.
4. Title: Alternative Benefit Plans (ABPs)
Type of Request: Extension of a currently approved collection.
CMS ID Number: CMS-10434 #3.
OMB Control Number: 0938-1188.
eRulemaking Docket ID Number: CMS-2023-0083.
Docket Web Address: https://www.regulations.gov/docket/CMS-2023-0083.
For Policy Related Questions, Contact: Adrienne Delozier at 410-
786-0278.
5. Title: Medicaid State Plan Eligibility
Type of Request: Extension of a currently approved collection.
CMS ID Number: CMS-10434 #15.
OMB Control Number: 0938-1188.
eRulemaking Docket ID Number: CMS-2023-0090.
Docket Web Address: https://www.regulations.gov/docket/CMS-2023-0090.
For Policy Related Questions, Contact: Suzette Seng at 410-786-
4703.
6. Title: Health Home State Plan Amendment (SPA)
Type of Request: Extension of a currently approved collection.
CMS ID Number: CMS-10434 #22.
OMB Control Number: 0938-1188.
eRulemaking Docket ID Number: CMS-2023-0084.
Docket Web Address: https://www.regulations.gov/docket/CMS-2023-0084.
For Policy Related Questions, Contact: Mary Pat Farkas at 410-786-
5731.
7. Title: Medicaid Adult and Child Core Set Measures
Type of Request: Extension of a currently approved collection.
CMS ID Number: CMS-10434 #26.
OMB Control Number: 0938-1188.
eRulemaking Docket ID Number: CMS-2023-0085.
Docket Web Address: https://www.regulations.gov/docket/CMS-2023-0085.
For Policy Related Questions, Contact: Virginia (Gigi) Raney at
410-786-6117.
8. Title: Maternal and Infant Health Quality
Type of Request: Extension of a currently approved collection.
CMS ID Number: CMS-10434 #45.
OMB Control Number: 0938-1188.
eRulemaking Docket ID Number: CMS-2023-0086.
Docket Web Address: https://www.regulations.gov/docket/CMS-2023-0086.
For Policy Related Questions, Contact: Virginia (Gigi) Raney at
410-786-6117.
9. Title: Health Home Core Sets
Type of Request: Extension of a currently approved collection.
CMS ID Number: CMS-10434 #47.
OMB Control Number: 0938-1188.
eRulemaking Docket ID Number: CMS-2023-0087.
Docket Web Address: https://www.regulations.gov/docket/CMS-2023-0087.
For Policy Related Questions, Contact: Mary Pat Farkas at 410-786-
5731.
[[Page 30379]]
10. Title: Medicaid Extended Postpartum Coverage and Continuous
Eligibility for Children
Type of Request: Extension of a currently approved collection.
CMS ID Number: CMS-10434 #77.
OMB Control Number: 0938-1188.
eRulemaking Docket ID Number: CMS-2023-0088.
Docket Web Address: https://www.regulations.gov/docket/CMS-2023-0088.
For Policy Related Questions, Contact: Alexa Turner at 410-786-
8823.
William N. Parham, III,
Director, Division of Information Collections and Regulatory Impacts,
Office of Strategic Operations and Regulatory Affairs.
[FR Doc. 2024-08658 Filed 4-22-24; 8:45 am]
BILLING CODE 4120-01-P