Proposed Data Collection Submitted for Public Comment and Recommendations, 85213-85215 [2024-24921]
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Federal Register / Vol. 89, No. 207 / Friday, October 25, 2024 / Notices
(Authority: Government in the Sunshine
Act, 5 U.S.C. 552b)
Vicktoria J. Allen,
Deputy Secretary of the Commission.
[FR Doc. 2024–25018 Filed 10–23–24; 4:15 pm]
BILLING CODE 6715–01–P
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ddrumheller on DSK120RN23PROD with NOTICES1
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than November 12, 2024.
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(Colette A. Fried, Assistant Vice
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Comments can also be sent
electronically to
Comments.applications@chi.frb.org:
1. The Deborah A. Talen Trust,
Deborah A. Talen, as trustee, both of
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17:40 Oct 24, 2024
Jkt 265001
Minneapolis, Minnesota; to become a
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sf.fisc.comments.applications@
sf.frb.org:
1. Russell S. Colombo, Walla Walla,
Washington; to join Megan F. Clubb and
Clifford W. Kontos, both of Walla Walla,
Washington, a group acting in concert,
to control voting shares of Baker Boyer
Bancorp, and thereby indirectly control
voting shares of Baker Boyer National
Bank, both of Walla Walla, Washington.
Board of Governors of the Federal Reserve
System.
Michele Taylor Fennell,
Associate Secretary of the Board.
[FR Doc. 2024–24898 Filed 10–24–24; 8:45 am]
FEDERAL TRADE COMMISSION
Senior Executive Service Performance
Review Board
Federal Trade Commission
(FTC).
ACTION:
Notice.
Notice is hereby given of the
appointment of members to the FTC
Performance Review Board.
FOR FURTHER INFORMATION CONTACT:
Tamika Williams, Acting Chief Human
Capital Officer, 600 Pennsylvania
Avenue NW, Washington, DC 20580,
(202) 326–2184.
SUPPLEMENTARY INFORMATION:
Publication of the Performance Review
Board (PRB) membership is required by
5 U.S.C. 4314(c)(4). The PRB reviews
and evaluates the initial appraisal of a
senior executive’s performance by the
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Performance Review Board:
Monique Fortenberry, Director, Office of
Workplace Inclusivity & Opportunity
Robin Moore, Principal Deputy General
Counsel
Maribeth Petrizzi, Assistant Director for
Compliance, Bureau of Competition
SUMMARY:
PO 00000
Frm 00078
David Robbins, Executive Director, PRB
Chair
Ted Rosenbaum, Deputy Director for
Research and Management, Bureau of
Economics
Rebecca Unruh, Deputy Director,
Bureau of Consumer Protection
Tamika Williams, Acting Chief Human
Capital Officer
By direction of the Commission.
April J. Tabor,
Secretary.
[FR Doc. 2024–24904 Filed 10–24–24; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–25–0612; Docket No. CDC–2024–
0083]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
BILLING CODE P
AGENCY:
85213
Fmt 4703
Sfmt 4703
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other federal
agencies the opportunity to comment on
a continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Well-Integrated
Screening and Evaluation for Women
Across the Nation (WISEWOMAN)
Reporting System. The WISEWOMAN
program is designed to prevent, detect,
and control, hypertension and other
cardiovascular disease (CVD) risk
factors through services such as health
coaching, and evidence informed
lifestyle programs, which are tailored
for individual and group behavior
change.
SUMMARY:
CDC must receive written
comments on or before December 24,
2024.
DATES:
You may submit comments,
identified by Docket No. CDC–2024–
0083 by of either the following methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
ADDRESSES:
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Federal Register / Vol. 89, No. 207 / Friday, October 25, 2024 / Notices
Disease Control and Prevention, 1600
Clifton Road NE, MS H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.regulations.gov )or by U.S. mail to
the address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS
H21–8, Atlanta, Georgia 30329;
Telephone: 404–639–7118; Email: omb@
cdc.gov.
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. In addition, the PRA also
requires federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. 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 submissions
of responses; and
5. Assess information collection costs.
Proposed Project
Well-Integrated Screening and
Evaluation for Women Across the
Nation (WISEWOMAN) Reporting
System (OMB Control No. 0920–0612,
Exp. 3/31/2025)—Revision—National
Center for Chronic Disease and
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Well-Integrated Screening and
Evaluation for Women Across the
Nation (WISEWOMAN) program
sponsored by the CDC, provides services
to low income, uninsured, or
underinsured women aged 35–64. The
WISEWOMAN program is designed to
prevent, detect, and control
hypertension and other cardiovascular
disease (CVD) risk factors through
healthy behavior support services which
are tailored for individual and group
behavior change. The WISEWOMAN
program provides services to
participants who are jointly enrolled in
the National Breast and Cervical Cancer
Early Detection Program (NBCCEDP),
which is also administered by CDC.
The WISEWOMAN program is
administered by state health
departments and tribal programs. In
2023, a new five-year cooperative
agreement was awarded under Funding
Opportunity Announcement DP23–
0003, subject to the availability of funds.
CDC collects two types of information
from WISEWOMAN awardees. The
WISEWOMAN awardee submits an
electronic data file to CDC twice per
year. The Minimum Data Elements
(MDE) file contains data using a unique
identifier with client-level information
about CVD risk factors and types of
healthy behavior support services for
participants served by the program. The
estimated burden per response for the
MDE file is 25 hours. The Annual
Progress Report provides a narrative
summary of each awardee’s objectives
and the activities undertaken to meet
program goals. The estimated burden
per response is 16 hours.
The WISEWOMAN Program is
requesting three additional years to
continue data collection. The 2024 OMB
Directive 15 for a combined race and
ethnicity question will replace the
separate race and ethnicity minimum
data elements. Two MDEs are being
deleted and two MDEs are being added,
and a response option is being added to
one MDE. There are no changes to
overall burden. CDC will continue to
use the information collected from
WISEWOMAN awardees to support
program monitoring and improvement
activities, program assessment, and
evaluation of program outcomes. The
overall program evaluation helps to
demonstrate program accomplishments
and strengthen the evidence for strategy
implementation for improved
engagement of underserved populations.
It can also determine whether the
identified strategies and associated
activities can be implemented at various
levels within a state or tribal
organization. The data collection is
designed to demonstrate how
WISEWOMAN can obtain CVD health
outcome data on at-risk populations,
promote public education about CVD
risk-factors, and improve the availability
of healthy behavior support services for
under-served participants.
This is a Revision for the
WISEWOMAN information collection
(OMB Control No. 0920–0612, Exp. 03/
31/2025). Participation in this
information collection is required as a
condition of cooperative agreement
funding. There are no costs to
respondents other than their time. The
total estimated annual burden hours are
2,640.
ddrumheller on DSK120RN23PROD with NOTICES1
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hrs.)
Total
burden
(in hrs.)
Type of respondents
Form name
WISEWOMAN Awardees ...........
Screening and Assessment and Lifestyle Program MDEs .............
Annual Progress Report ..................................................................
40
40
2
1
25
16
2,000
640
Total .....................................
..........................................................................................................
......................
..........................
....................
2,640
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Federal Register / Vol. 89, No. 207 / Friday, October 25, 2024 / Notices
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2024–24921 Filed 10–24–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–25–1385; Docket No. CDC–2024–
0084]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other federal
agencies the opportunity to comment on
a continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Characteristics
of Cases of Priority Fungal Diseases.
These case report forms (CRF) collect
information on patient demographics,
underlying conditions, diagnosis,
treatments, healthcare utilization, and
outcomes of patients with
coccidioidomycosis, histoplasmosis,
blastomycosis, Candida auris, triazoleresistant Aspergillus fumigatus infection
or colonization, or antifungal-resistant
dermatophytosis, chromoblastomycosis,
mycetoma, and sporotrichosis.
DATES: CDC must receive written
comments on or before December 24,
2024.
SUMMARY:
You may submit comments,
identified by Docket No. CDC–2024–
0084 by either of the following methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
www.regulations.gov.
ddrumheller on DSK120RN23PROD with NOTICES1
ADDRESSES:
VerDate Sep<11>2014
17:40 Oct 24, 2024
Jkt 265001
Please note: Submit all comments
through the Federal eRulemaking portal
(www.regulations.gov) or by U.S. mail to
the address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS
H21–8, Atlanta, Georgia 30329;
Telephone: 404–639–7570; Email: omb@
cdc.gov.
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. In addition, the PRA also
requires federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. 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 submissions
of responses; and
5. Assess information collection costs.
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
PO 00000
Frm 00080
Fmt 4703
Sfmt 4703
85215
(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.
CDC plans 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 to the
information collection project
Characteristics of Cases of Priority
Fungal Diseases (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, Case Report Forms
(CRF) have also been developed for
chromoblastomycosis, mycetoma, and
sporotrichosis.
CDC plans 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 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.
E:\FR\FM\25OCN1.SGM
25OCN1
]]>Agencies
[Federal Register Volume 89, Number 207 (Friday, October 25, 2024)]
[Notices]
[Pages 85213-85215]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-24921]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-25-0612; Docket No. CDC-2024-0083]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
federal agencies the opportunity to comment on a continuing information
collection, as required by the Paperwork Reduction Act of 1995. This
notice invites comment on a proposed information collection project
titled Well-Integrated Screening and Evaluation for Women Across the
Nation (WISEWOMAN) Reporting System. The WISEWOMAN program is designed
to prevent, detect, and control, hypertension and other cardiovascular
disease (CVD) risk factors through services such as health coaching,
and evidence informed lifestyle programs, which are tailored for
individual and group behavior change.
DATES: CDC must receive written comments on or before December 24,
2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0083 by of either the following methods:
Federal eRulemaking Portal: www.regulations.gov. Follow
the instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for
[[Page 85214]]
Disease Control and Prevention, 1600 Clifton Road NE, MS H21-8,
Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to www.regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (www.regulations.gov )or by U.S. mail to the address listed
above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS H21-8, Atlanta, Georgia 30329; Telephone: 404-639-7118;
Email: [email protected].
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. In addition, the PRA also requires
federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. 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;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected;
4. 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
submissions of responses; and
5. Assess information collection costs.
Proposed Project
Well-Integrated Screening and Evaluation for Women Across the
Nation (WISEWOMAN) Reporting System (OMB Control No. 0920-0612, Exp. 3/
31/2025)--Revision--National Center for Chronic Disease and Prevention
and Health Promotion (NCCDPHP), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Well-Integrated Screening and Evaluation for Women Across the
Nation (WISEWOMAN) program sponsored by the CDC, provides services to
low income, uninsured, or underinsured women aged 35-64. The WISEWOMAN
program is designed to prevent, detect, and control hypertension and
other cardiovascular disease (CVD) risk factors through healthy
behavior support services which are tailored for individual and group
behavior change. The WISEWOMAN program provides services to
participants who are jointly enrolled in the National Breast and
Cervical Cancer Early Detection Program (NBCCEDP), which is also
administered by CDC.
The WISEWOMAN program is administered by state health departments
and tribal programs. In 2023, a new five-year cooperative agreement was
awarded under Funding Opportunity Announcement DP23-0003, subject to
the availability of funds. CDC collects two types of information from
WISEWOMAN awardees. The WISEWOMAN awardee submits an electronic data
file to CDC twice per year. The Minimum Data Elements (MDE) file
contains data using a unique identifier with client-level information
about CVD risk factors and types of healthy behavior support services
for participants served by the program. The estimated burden per
response for the MDE file is 25 hours. The Annual Progress Report
provides a narrative summary of each awardee's objectives and the
activities undertaken to meet program goals. The estimated burden per
response is 16 hours.
The WISEWOMAN Program is requesting three additional years to
continue data collection. The 2024 OMB Directive 15 for a combined race
and ethnicity question will replace the separate race and ethnicity
minimum data elements. Two MDEs are being deleted and two MDEs are
being added, and a response option is being added to one MDE. There are
no changes to overall burden. CDC will continue to use the information
collected from WISEWOMAN awardees to support program monitoring and
improvement activities, program assessment, and evaluation of program
outcomes. The overall program evaluation helps to demonstrate program
accomplishments and strengthen the evidence for strategy implementation
for improved engagement of underserved populations. It can also
determine whether the identified strategies and associated activities
can be implemented at various levels within a state or tribal
organization. The data collection is designed to demonstrate how
WISEWOMAN can obtain CVD health outcome data on at-risk populations,
promote public education about CVD risk-factors, and improve the
availability of healthy behavior support services for under-served
participants.
This is a Revision for the WISEWOMAN information collection (OMB
Control No. 0920-0612, Exp. 03/31/2025). Participation in this
information collection is required as a condition of cooperative
agreement funding. There are no costs to respondents other than their
time. The total estimated annual burden hours are 2,640.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total
Type of respondents Form name respondents responses per response burden (in
respondent (in hrs.) hrs.)
----------------------------------------------------------------------------------------------------------------
WISEWOMAN Awardees............... Screening and 40 2 25 2,000
Assessment and
Lifestyle Program
MDEs.
Annual Progress 40 1 16 640
Report.
--------------------------------------------------------
Total........................ .................... ............ ............... ........... 2,640
----------------------------------------------------------------------------------------------------------------
[[Page 85215]]
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2024-24921 Filed 10-24-24; 8:45 am]
BILLING CODE 4163-18-P
