Agency Forms Undergoing Paperwork Reduction Act Review, 2704-2706 [2025-00454]
Download as PDF
2704
Federal Register / Vol. 90, No. 7 / Monday, January 13, 2025 / Notices
The Director, Office of Strategic
Business Initiatives, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, Centers for Disease Control and
Prevention.
30341–3717. Telephone: (404) 718–
7664; Email: CBarrett@cdc.gov.
The Director, Office of Strategic
Business Initiatives, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2025–00492 Filed 1–10–25; 8:45 am]
BILLING CODE 4163–18–P
[FR Doc. 2025–00488 Filed 1–10–25; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Centers for Disease Control and
Prevention
ddrumheller on DSK120RN23PROD with NOTICES1
Notice of Closed Meeting
Pursuant to 5 U.S.C. 1009(d), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended, and the Determination of
the Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, Centers for Disease Control and
Prevention, pursuant to Public Law 92–
463. The grant applications and the
discussions could disclose confidential
trade secrets or commercial property
such as patentable material, and
personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Disease,
Disability, and Injury Prevention and
Control Special Emphasis Panel (SEP)—
DP25–041, Connecting Organizations
and People to Empower Diabetes
Prevention and Treatment
(Connections).
Date: March 11, 2025.
Time: 10 a.m.–6 p.m., EDT.
Place: Teleconference/Web
Conference.
Agenda: To review and evaluate grant
applications.
For Further Information Contact:
Catherine Barrett, Ph.D., Scientific
Review Officer, National Center for
Chronic Disease Prevention and Health
Promotion, Centers for Disease Control
and Prevention, 4770 Buford Highway,
Mailstop S106–3, Atlanta, Georgia
VerDate Sep<11>2014
18:48 Jan 09, 2025
Jkt 265001
Notice of Closed Meeting
Pursuant to 5 U.S.C. 1009(d), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended, and the Determination of
the Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, Centers for Disease Control and
Prevention, pursuant to Public Law 92–
463. The grant applications and the
discussions could disclose confidential
trade secrets or commercial property
such as patentable material, and
personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Disease,
Disability, and Injury Prevention and
Control Special Emphasis Panel (SEP)—
RFA–OH–24–002, Exploratory/
Developmental Grants on Lifestyle
Medicine Research Related to the World
Trade Center Health Program (R21);
RFA–OH–24–003, Exploratory/
Developmental Grants Related to the
World Trade Center Survivors (R21-No
Applications with Responders
Accepted); RFA–OH–24–004, World
Trade Center Health Program Mentored
Research Scientist Career Development
Award (K01); and RFA–OH–25–001,
Exploratory/Developmental Research for
World Trade Center Health Program
Evidence-based Strategies to Improve
Treatment Effectiveness, Diagnostic
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Practices, and Program Evaluation
(R21).
Dates and Times: February 25, 2025,
9 a.m.–5 p.m., EST; and February 26,
2025, 9 a.m.–12 p.m., EST.
Place: Courtyard by Marriott Atlanta
Decatur Downtown/Emory, 130
Clairemont Avenue, Decatur, Georgia
30030.
Agenda: To review and evaluate grant
applications.
For Further Information Contact:
Laurel Garrison, M.P.H., Scientific
Review Officer, Office of Extramural
Coordination and Special Projects,
National Institute for Occupational
Safety and Health, Centers for Disease
Control and Prevention, 5555 Ridge
Avenue, Cincinnati, Ohio 45213.
Telephone: (513) 533–8324; Email:
LGarrison@cdc.gov.
The Director, Office of Strategic
Business Initiatives, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2025–00487 Filed 1–10–25; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–25–1385]
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Characteristics
of Cases of Priority Fungal Diseases’’ to
the Office of Management and Budget
(OMB) for review and approval. CDC
previously published a ‘‘Proposed Data
Collection Submitted for Public
Comment and Recommendations’’
notice on October 25, 2024, to obtain
comments from the public and affected
agencies. CDC did not receive comments
related to the previous notice. This
notice serves to allow an additional 30
days for public and affected agency
comments.
E:\FR\FM\13JAN1.SGM
13JAN1
2705
Federal Register / Vol. 90, No. 7 / Monday, January 13, 2025 / Notices
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
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. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Characteristics of Cases of Priority
Fungal Diseases (OMB Control No.
0920–1385, Exp. 4/30/2027)—
Revision—National Center for Emerging
and Zoonotic Infectious Diseases
(NCEZID), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Fungal diseases cause substantial
illness, ranging from mild infection to
severe or life-threatening invasive
disease. They also constitute a
considerable financial burden on
patients and healthcare systems.
Awareness of fungal diseases is low,
and data collection has historically been
limited in size, scope, and coordination,
which has hindered our understanding
of these diseases. Detailed
epidemiologic and clinical data are
critical to inform appropriate public
health responses. We plan to enhance
surveillance of high priority fungal
diseases across the United States to
better characterize factors such as
disease burden, geographic scope,
patient risk factors, health disparities,
healthcare utilization, outcomes, and
emerging trends. This project will serve
as a Revision of the information
collections project: Characteristics of
Cases of Priority Fungal Diseases Case
Report Form (CRF) (OMB Control No.
0920–1385). The Revision will expand
the number of fungal diseases for which
data may be collected.
In addition to triazole-resistant A.
fumigatus infections,
coccidioidomycosis, histoplasmosis,
blastomycosis, C. auris, and antifungalresistant dermatophytosis, CRFs have
also been developed for
chromoblastomycosis, mycetoma, and
sporotrichosis. We plan to use
standardized CRFs to collect public
health surveillance data for cases of
these diseases regarding demographics
(e.g., age, sex, race/ethnicity, location of
residence), underlying medical
conditions, diagnosis (e.g., clinical
presentation, laboratory testing),
treatments, and outcomes (e.g.,
hospitalization, vital status). The
corresponding CRF would be filled out
voluntarily by State, local or Tribal
health departments, Federal agencies,
and the members of the private sector
(e.g., academic institutions) and
contains a section for medical chart
review and an optional supplemental
interview (including data on potential
occupational or environmental
exposures) of the patient or their
representative.
Findings can help identify
populations at higher risk of these
diseases, detect emerging epidemiologic
trends, and guide prevention and
response efforts. They can also help
better focus public and healthcare
provider outreach, inform efforts to
contain or mitigate spread, and
influence health policy and research on
prevention and treatment.
CDC requests OMB approval for an
estimated 1,564 annual burden hours.
There is no cost to respondents other
than their time to participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Type of
respondent
Triazole-resistant Aspergillus fumigatus Case Report Form (Attachment 3a).
Coccidioidomycosis Case Report Form (Attachment 3b) ............
State and Local Health
Departments.
State and Local Health
Departments.
Private Sectors .................
State and Local Health
Departments.
Private Sectors .................
State and Local Health
Departments.
Private Sectors .................
State and Local Health
Departments.
Private Sectors .................
State and Local Health
Departments.
Private Sectors .................
Private Sectors .................
Private Sectors .................
Histoplasmosis Case Report Form (Attachment 3c) ....................
ddrumheller on DSK120RN23PROD with NOTICES1
Blastomycosis Case Report Form (Attachment 3d) .....................
Candida auris Case Report Form (Attachment 3e) .....................
Antifungal-resistant dermatophytosis case report form (Attachment 3f).
Chromoblastomycosis case report form (Attachment 3g) ............
Mycetoma case report form (Attachment 3h) ...............................
Sporotrichosis case report form (Attachment 3i) ..........................
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Number of
respondents
E:\FR\FM\13JAN1.SGM
Number
responses per
respondent
Avg. burden
per response
(in hrs.)
15
15
0.5
10
25
1.0
3
10
10
25
1.0
1.0
3
10
10
25
1.0
1.0
3
15
10
20
1.0
0.75
3
10
10
10
0.75
0.5
25
25
25
10
5
10
0.5
0.5
0.5
13JAN1
2706
Federal Register / Vol. 90, No. 7 / Monday, January 13, 2025 / Notices
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. 2025–00454 Filed 1–10–25; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3469–PN]
Medicare and Medicaid Programs:
Application From The Joint
Commission for Continued Approval of
its Hospice Accreditation Program
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice with request for
comment.
AGENCY:
This proposed notice
acknowledges the receipt of an
application from The Joint Commission
for continued recognition as a national
accrediting organization for hospices
that wish to participate in the Medicare
or Medicaid programs.
DATES: To be assured consideration,
comments must be received at one of
the addresses provided below, no later
than 5 p.m. on February 12, 2025.
ADDRESSES: In commenting, refer to file
code CMS–3469–PN.
Comments, including mass comment
submissions, must be submitted in one
of the following three ways (please
choose only one of the ways listed):
1. Electronically. You may submit
electronic comments on this regulation
to https://www.regulations.gov . Follow
the ‘‘Submit a comment’’ instructions.
2. By regular mail. You may mail
written comments to the following
address ONLY:
Centers for Medicare & Medicaid
Services, Department of Health and
Human Services, Attention: CMS–3469–
PN, P.O. Box 8010, Baltimore, MD
21244–8010.
Please allow sufficient time for mailed
comments to be received before the
close of the comment period.
3. By express or overnight mail. You
may send written comments to the
following address ONLY:
Centers for Medicare & Medicaid
Services, Department of Health and
Human Services, Attention: CMS–3469–
PN, Mail Stop C4–26–05, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
FOR FURTHER INFORMATION CONTACT:
Lillian Williams, (410) 786–8636 or
Melissa Rice, (410) 786–3270.
ddrumheller on DSK120RN23PROD with NOTICES1
SUMMARY:
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18:48 Jan 09, 2025
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SUPPLEMENTARY INFORMATION:
Inspection of Public Comments: All
comments received before the close of
the comment period are available for
viewing by the public, including any
personally identifiable or confidential
business information that is included in
a comment. We post all comments
received before the close of the
comment period on the following
website as soon as possible after they
have been received: https://
www.regulations.gov. Follow the search
instructions on that website to view
public comments. CMS will not post on
Regulations.gov public comments that
make threats to individuals or
institutions or suggest that the
commenter will take actions to harm an
individual. CMS continues to encourage
individuals not to submit duplicative
comments. We will post acceptable
comments from multiple unique
commenters even if the content is
identical or nearly identical to other
comments.
I. Background
Under the Medicare program, eligible
beneficiaries may receive covered
services in a hospice, provided that
certain requirements are met by the
hospice. Section 1861(dd) of the Social
Security Act (the Act) establishes
distinct criteria for facilities seeking
designation as a hospice. Regulations
concerning provider agreements are at
42 CFR part 489 and those pertaining to
activities relating to the survey and
certification of facilities are at 42 CFR
part 488. The regulations at 42 CFR part
418 specify the conditions that a
hospice must meet in order to
participate in the Medicare program, the
scope of covered services and the
conditions for Medicare payment for
hospice services.
Generally, to enter into an agreement,
a hospice must first be certified by a
state survey agency (SA) as complying
with the conditions or requirements set
forth in part 418. Thereafter, the hospice
is subject to regular surveys by a SA to
determine whether it continues to meet
these requirements.
However, section 1865(a)(1) of the Act
provides that, if a provider entity
demonstrates through accreditation by a
Centers for Medicare & Medicaid
Services (CMS) approved national
Accrediting Organization (AO) that all
applicable Medicare conditions are met
or exceeded, we will deem those
provider entities as having met the
requirements. Accreditation by an AO is
voluntary and is not required for
Medicare participation.
If an AO is recognized by the
Secretary of the Department of Health
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Frm 00043
Fmt 4703
Sfmt 4703
and Human Services (the Secretary) as
having standards for accreditation that
meet or exceed Medicare requirements,
any provider entity accredited by the
national accrediting body’s approved
program would be deemed to meet the
Medicare conditions. A national AO
applying for approval of its
accreditation program under part 488,
subpart A, must provide CMS with
reasonable assurance that the AO
requires the accredited provider entities
to meet requirements that are at least as
stringent as the Medicare conditions.
Our regulations concerning the approval
of AOs are set forth at §§ 488.4 and
488.5. The regulations at § 488.5(e)(2)(i)
require AOs to reapply for continued
approval of its accreditation program
every 6 years or sooner as determined
by CMS.
The Joint Commission’s (TJC’s)
current term of approval for their
hospice accreditation program expires
June 18, 2025.
II. Approval of Deeming Organizations
Section 1865(a)(2) of the Act and our
regulations at § 488.5 require that our
findings concerning review and
approval of a national AO’s
requirements consider, among other
factors, the applying AO’s requirements
for accreditation; survey procedures;
resources for conducting required
surveys; capacity to furnish information
for use in enforcement activities;
monitoring procedures for provider
entities found not in compliance with
the conditions or requirements; and
ability to provide CMS with the
necessary data for validation.
Section 1865(a)(3)(A) of the Act
further requires that we publish, within
60 days of receipt of an organization’s
complete application, a notice
identifying the national accrediting
body making the request, describing the
nature of the request, and providing at
least a 30-day public comment period.
We have 210 days from the receipt of a
complete application to publish notice
of approval or denial of the application.
The purpose of this proposed notice
is to inform the public of TJC’s request
for continued approval of its hospice
accreditation program. This notice also
solicits public comment on whether
TJC’s requirements meet or exceed the
Medicare conditions of participation
(CoPs) for hospices.
III. Evaluation of Deeming Authority
Request
TJC submitted all the necessary
materials to enable us to make a
determination concerning its request for
continued approval of its hospice
accreditation program. This application
E:\FR\FM\13JAN1.SGM
13JAN1
Agencies
[Federal Register Volume 90, Number 7 (Monday, January 13, 2025)]
[Notices]
[Pages 2704-2706]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2025-00454]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-25-1385]
Agency Forms Undergoing Paperwork Reduction Act Review
In accordance with the Paperwork Reduction Act of 1995, the Centers
for Disease Control and Prevention (CDC) has submitted the information
collection request titled ``Characteristics of Cases of Priority Fungal
Diseases'' to the Office of Management and Budget (OMB) for review and
approval. CDC previously published a ``Proposed Data Collection
Submitted for Public Comment and Recommendations'' notice on October
25, 2024, to obtain comments from the public and affected agencies. CDC
did not receive comments related to the previous notice. This notice
serves to allow an additional 30 days for public and affected agency
comments.
[[Page 2705]]
CDC will accept all comments for this proposed information
collection project. The Office of Management and Budget is particularly
interested in comments that:
(a) Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
(b) Evaluate the accuracy of the agencies estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and clarity of the information to
be collected;
(d) Minimize the burden of the collection of information on those
who are to respond, including, through the use of appropriate
automated, electronic, mechanical, or other technological collection
techniques or other forms of information technology, e.g., permitting
electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570. 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. Direct
written comments and/or suggestions regarding the items contained in
this notice to the Attention: CDC Desk Officer, Office of Management
and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202)
395-5806. Provide written comments within 30 days of notice
publication.
Proposed Project
Characteristics of Cases of Priority Fungal Diseases (OMB Control
No. 0920-1385, Exp. 4/30/2027)--Revision--National Center for Emerging
and Zoonotic Infectious Diseases (NCEZID), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Fungal diseases cause substantial illness, ranging from mild
infection to severe or life-threatening invasive disease. They also
constitute a considerable financial burden on patients and healthcare
systems. Awareness of fungal diseases is low, and data collection has
historically been limited in size, scope, and coordination, which has
hindered our understanding of these diseases. Detailed epidemiologic
and clinical data are critical to inform appropriate public health
responses. We plan to enhance surveillance of high priority fungal
diseases across the United States to better characterize factors such
as disease burden, geographic scope, patient risk factors, health
disparities, healthcare utilization, outcomes, and emerging trends.
This project will serve as a Revision of the information collections
project: Characteristics of Cases of Priority Fungal Diseases Case
Report Form (CRF) (OMB Control No. 0920-1385). The Revision will expand
the number of fungal diseases for which data may be collected.
In addition to triazole-resistant A. fumigatus infections,
coccidioidomycosis, histoplasmosis, blastomycosis, C. auris, and
antifungal-resistant dermatophytosis, CRFs have also been developed for
chromoblastomycosis, mycetoma, and sporotrichosis. We plan to use
standardized CRFs to collect public health surveillance data for cases
of these diseases regarding demographics (e.g., age, sex, race/
ethnicity, location of residence), underlying medical conditions,
diagnosis (e.g., clinical presentation, laboratory testing),
treatments, and outcomes (e.g., hospitalization, vital status). The
corresponding CRF would be filled out voluntarily by State, local or
Tribal health departments, Federal agencies, and the members of the
private sector (e.g., academic institutions) and contains a section for
medical chart review and an optional supplemental interview (including
data on potential occupational or environmental exposures) of the
patient or their representative.
Findings can help identify populations at higher risk of these
diseases, detect emerging epidemiologic trends, and guide prevention
and response efforts. They can also help better focus public and
healthcare provider outreach, inform efforts to contain or mitigate
spread, and influence health policy and research on prevention and
treatment.
CDC requests OMB approval for an estimated 1,564 annual burden
hours. There is no cost to respondents other than their time to
participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number Avg. burden
Form name Type of respondent Number of responses per per response
respondents respondent (in hrs.)
----------------------------------------------------------------------------------------------------------------
Triazole-resistant Aspergillus State and Local Health 15 15 0.5
fumigatus Case Report Form Departments.
(Attachment 3a).
Coccidioidomycosis Case Report Form State and Local Health 10 25 1.0
(Attachment 3b). Departments.
Private Sectors......... 3 10 1.0
Histoplasmosis Case Report Form State and Local Health 10 25 1.0
(Attachment 3c). Departments.
Private Sectors......... 3 10 1.0
Blastomycosis Case Report Form State and Local Health 10 25 1.0
(Attachment 3d). Departments.
Private Sectors......... 3 10 1.0
Candida auris Case Report Form State and Local Health 15 20 0.75
(Attachment 3e). Departments.
Private Sectors......... 3 10 0.75
Antifungal-resistant dermatophytosis State and Local Health 10 10 0.5
case report form (Attachment 3f). Departments.
Chromoblastomycosis case report form Private Sectors......... 25 10 0.5
(Attachment 3g).
Mycetoma case report form (Attachment Private Sectors......... 25 5 0.5
3h).
Sporotrichosis case report form Private Sectors......... 25 10 0.5
(Attachment 3i).
----------------------------------------------------------------------------------------------------------------
[[Page 2706]]
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. 2025-00454 Filed 1-10-25; 8:45 am]
BILLING CODE 4163-18-P