Proposed Data Collection Submitted for Public Comment and Recommendations, 14501-14503 [2024-03889]
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<![CDATA[
14501
Federal Register / Vol. 89, No. 39 / Tuesday, February 27, 2024 / Notices
of the Public Health Service Act, a
Certificate of Confidentiality (CoC)
applies to this research. The total
estimated burden hours are 109 for the
field study and 77 for the environmental
chamber study. There are no costs to
respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Number of
respondents
Form name
Number
responses
per
respondent
Average
burden per
response
(hours)
Field study
Miners
Miners
Miners
Miners
Miners
Miners
.............................................................
.............................................................
.............................................................
.............................................................
.............................................................
.............................................................
Informed consent form (field) .........................
Initial health screening questionnaire (field) ..
Pre-shift field questionnaire ...........................
Mid-shift field questionnaire ...........................
PVT cognitive test ..........................................
Post-shift field questionnaire ..........................
59
59
59
59
59
59
1
1
2
4
5
2
30/60
30/60
5/60
1/60
5/60
5/60
30
30
30
1
1
1
30/60
10/60
30/60
5
30
30
30
30
30
1
5
5
5
5
2
1/60
1/60
2/60
10/60
1/60
5/60
Chamber study
Miners/firefighters/construction workers .........
Miners/firefighters/construction workers .........
Miners/firefighters/construction workers .........
Miners/firefighters/construction
Miners/firefighters/construction
Miners/firefighters/construction
Miners/firefighters/construction
Miners/firefighters/construction
Miners/firefighters/construction
workers
workers
workers
workers
workers
workers
.........
.........
.........
.........
.........
.........
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. 2024–03883 Filed 2–26–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–0978; Docket No. CDC–2024–
0013]
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 proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
lotter on DSK11XQN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
16:53 Feb 26, 2024
Jkt 262001
Informed consent form (chamber) .................
Physical examination form .............................
Initial health ....................................................
screening questionnaire (chamber) ...............
Release of information form ...........................
TSS and RPE .................................................
PANAS and KSS ............................................
Cognitive test: PVT ........................................
Cognitive test: N-back ....................................
Pre-testing health questionnaire ....................
titled Emerging Infections Program
(EIP). EIP is a population-based
surveillance activity conducted via
active, laboratory case finding that is
used for detecting, identifying, and
monitoring emerging pathogens.
DATES: CDC must receive written
comments on or before April 29, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0013 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.
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;
PO 00000
Frm 00072
Fmt 4703
Sfmt 4703
Telephone: 404–639–7570; Email: omb@
cdc.gov.
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;
SUPPLEMENTARY INFORMATION:
E:\FR\FM\27FEN1.SGM
27FEN1
14502
Federal Register / Vol. 89, No. 39 / Tuesday, February 27, 2024 / Notices
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.
Background and Brief Description
The Emerging Infections Programs
(EIPs) are population-based centers of
excellence established through a
network of state health departments
collaborating with academic
institutions; local health departments;
public health and clinical laboratories;
infection control professionals; and
healthcare providers. EIPs assist in
local, state, and national efforts to
prevent, control, and monitor the public
health impact of infectious diseases.
Activities of the EIPs fall into the
following general categories: (1) active
surveillance; (2) applied public health
epidemiologic and laboratory activities;
(3) implementation and evaluation of
pilot prevention/intervention projects;
and (4) flexible response to public
health emergencies. Activities of the
EIPs are designed to: (1) address issues
that the EIP network is particularly
suited to investigate; (2) maintain
Proposed Project
Emerging Infections Program (EIP)
(OMB Control No. 0920–0978, Exp. 2/
28/2026)—Revision—National Center
for Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
sufficient flexibility for emergency
response and new problems as they
arise; (3) develop and evaluate public
health interventions to inform public
health policy and treatment guidelines;
(4) incorporate training as a key
function; and (5) prioritize projects that
lead directly to the prevention of
disease.
A Revision is being submitted to make
existing collection instruments clearer,
consolidate forms and to add new
forms. These forms will allow the EIP to
better detect, identify, track changes in
laboratory testing methodology, gather
information about laboratory utilization
in the EIP catchment area to ensure that
all cases are being captured, and survey
EIP staff to evaluate program quality.
CDC requests OMB approval for an
estimated 42,440 annual burden hours.
There is no cost to respondents other
than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondent
Form number
State Health Department .....................
ABC.100.1
ABC.100.2
ABC.100.3
ABC.100.4
ABC.100.5
FN.200.1
FN.200.2
FN.200.3
FN.200.4
FN.200.5
FN.200.6
FN.200.7
FN.200.8
FN.200.9
FN.200.10
FSN.300.1
FSN.300.2
FSN.300.3
FSN.300.4
HAIC.400.1
lotter on DSK11XQN23PROD with NOTICES1
HAIC.400.2
HAIC.400.3
HAIC.400.4
HAIC.400.5
HAIC.400.6
VerDate Sep<11>2014
16:53 Feb 26, 2024
Jkt 262001
Number of
respondents
Form name
ABCs Case Report Form ....................
ABCs Invasive Pneumococcal Disease in Children and Adults Case
Report Form.
ABCs H. influenzae Neonatal Sepsis
Expanded Surveillance Form.
ABCs Severe GAS Infection Supplemental Form.
ABCs Neonatal Infection Expanded
Tracking Form.
FoodNet Campylobacter .....................
FoodNet Cyclospora ...........................
FoodNet Listeria monocytogenes .......
FoodNet Salmonella ...........................
FoodNet Shiga toxin producing E. coli
FoodNet Shigella ................................
FoodNet Vibrio ....................................
FoodNet Yersinia ................................
FoodNet Hemolytic Uremic Syndrome
FoodNet Clinical Laboratory Practices
and Testing Volume.
FluSurv-Net Influenza Hospitalization
Surveillance Network Case Report
Form.
FluSurv-Net Influenza Hospitalization
Surveillance Project Vaccination
Phone Script and Consent Form
(English/Spanish).
FluSurv-Net Influenza Hospitalization
Surveillance Project Provider Vaccination History Fax Form (Children/
Adults).
FluSurv-NET Laboratory Survey .........
HAIC—Multi-site Gram-Negative Surveillance Initiative (MuGSI) Case
Report Form.
HAIC MuGSI CA CP–CRE Health
interview.
HAIC MuGSI Supplemental Surveillance Officer Survey.
HAIC—Invasive
Staphylococcus
aureus Infection Case Report Form.
HAIC—Invasive
Staphylococcus
aureus Laboratory Survey.
HAIC—Invasive
Staphylococcus
aureus Supplemental Surveillance
Officers Survey.
PO 00000
Frm 00073
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
Average
burden
per response
(in hours)
Current
total burden
(in hours)
10
10
809
127
20/60
10/60
2697
212
10
6
10/60
10
10
136
20/60
453
10
37
20/60
123
10
10
10
10
10
10
10
10
10
10
970
42
16
855
290
234
46
55
10
70
21/60
10/60
20/60
21/60
20/60
10/60
10/60
10/60
1
10/60
3395
70
53
2993
967
390
77
92
100
117
15
727
25/60
4544
14
16
10/60
37
14
126
5/60
147
15
11
16
1581
10/60
29/60
40
8406
10
10
30/60
50
11
1
20/60
4
10
788
29/60
3809
10
11
9/60
17
10
1
10.5/60
2
E:\FR\FM\27FEN1.SGM
27FEN1
14503
Federal Register / Vol. 89, No. 39 / Tuesday, February 27, 2024 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Type of
respondent
Form number
HAIC.400.7
HAIC.400.13
HAIC—CDI Case Report and Treatment Form.
HAIC—Annual Survey of Laboratory
Testing Practices for C. difficile Infections.
HAIC—CDI Annual Surveillance Officers Survey.
HAIC—Emerging Infections Program
C. difficile Surveillance Nursing
Home Telephone Survey (LTCF).
HAIC Candidemia Case Report Form
HAIC—Laboratory Testing Practices
for Candidemia Questionnaire.
HAIC Death Ascertainment Project ....
........................
.............................................................
HAIC.400.8
HAIC.400.9
HAIC.400.10
HAIC.400.11
HAIC.400.12
Total .............................................
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. 2024–03889 Filed 2–26–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–24DD; Docket No. CDC–2024–
0012]
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 proposed information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Project
Confianza to Identify Medical Mistrust
Drivers among Hispanic/Latino Gay,
Bisexual, and Other Men Who Have Sex
With Men (HLMSM). The data
collection is designed to identify the
root causes of medical mistrust and
opportunities to implement
interventions that can make HIV-related
services trusted and acceptable for
HLMSM to increase access to, and
utilization of, HIV prevention and care
lotter on DSK11XQN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
16:53 Feb 26, 2024
Number of
respondents
Form name
Jkt 262001
Frm 00074
Fmt 4703
Sfmt 4703
Average
burden
per response
(in hours)
Current
total burden
(in hours)
10
1650
38/60
10450
10
16
17/60
45
10
1
15/60
3
10
45
5/60
38
10
10
170
20
40/60
14/60
1133
47
10
8
1440/60
1,920
........................
........................
........................
42,440
services, as well as contribute toward
achieving Ending the HIV Epidemic in
the U.S. (EHE) goals and National HIV
Strategic Plan health disparities goals.
DATES: CDC must receive written
comments on or before April 29, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0012 by either of the following methods:
b Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
b 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. 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
PO 00000
Number of
responses per
respondent
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
Project Confianza to Identify Medical
Mistrust Drivers among Hispanic/Latino
Gay, Bisexual, and Other Men Who
Have Sex With Men (HLMSM)—New—
National Center for HIV, Viral Hepatitis,
STD, and TB Prevention (NCHHSTP),
Centers for Disease Control and
Prevention (CDC).
E:\FR\FM\27FEN1.SGM
27FEN1
]]>Agencies
[Federal Register Volume 89, Number 39 (Tuesday, February 27, 2024)]
[Notices]
[Pages 14501-14503]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-03889]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-24-0978; Docket No. CDC-2024-0013]
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 proposed and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled Emerging Infections Program
(EIP). EIP is a population-based surveillance activity conducted via
active, laboratory case finding that is used for detecting,
identifying, and monitoring emerging pathogens.
DATES: CDC must receive written comments on or before April 29, 2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0013 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.
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: [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;
[[Page 14502]]
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
Emerging Infections Program (EIP) (OMB Control No. 0920-0978, Exp.
2/28/2026)--Revision--National Center for Emerging and Zoonotic
Infectious Diseases (NCEZID), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Emerging Infections Programs (EIPs) are population-based
centers of excellence established through a network of state health
departments collaborating with academic institutions; local health
departments; public health and clinical laboratories; infection control
professionals; and healthcare providers. EIPs assist in local, state,
and national efforts to prevent, control, and monitor the public health
impact of infectious diseases. Activities of the EIPs fall into the
following general categories: (1) active surveillance; (2) applied
public health epidemiologic and laboratory activities; (3)
implementation and evaluation of pilot prevention/intervention
projects; and (4) flexible response to public health emergencies.
Activities of the EIPs are designed to: (1) address issues that the EIP
network is particularly suited to investigate; (2) maintain sufficient
flexibility for emergency response and new problems as they arise; (3)
develop and evaluate public health interventions to inform public
health policy and treatment guidelines; (4) incorporate training as a
key function; and (5) prioritize projects that lead directly to the
prevention of disease.
A Revision is being submitted to make existing collection
instruments clearer, consolidate forms and to add new forms. These
forms will allow the EIP to better detect, identify, track changes in
laboratory testing methodology, gather information about laboratory
utilization in the EIP catchment area to ensure that all cases are
being captured, and survey EIP staff to evaluate program quality.
CDC requests OMB approval for an estimated 42,440 annual burden
hours. There is no cost to respondents other than their time.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Current total
Type of respondent Form number Form name respondents responses per response (in burden (in
respondent hours) hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
State Health Department................... ABC.100.1 ABCs Case Report Form....... 10 809 20/60 2697
ABC.100.2 ABCs Invasive Pneumococcal 10 127 10/60 212
Disease in Children and
Adults Case Report Form.
ABC.100.3 ABCs H. influenzae Neonatal 10 6 10/60 10
Sepsis Expanded
Surveillance Form.
ABC.100.4 ABCs Severe GAS Infection 10 136 20/60 453
Supplemental Form.
ABC.100.5 ABCs Neonatal Infection 10 37 20/60 123
Expanded Tracking Form.
FN.200.1 FoodNet Campylobacter....... 10 970 21/60 3395
FN.200.2 FoodNet Cyclospora.......... 10 42 10/60 70
FN.200.3 FoodNet Listeria 10 16 20/60 53
monocytogenes.
FN.200.4 FoodNet Salmonella.......... 10 855 21/60 2993
FN.200.5 FoodNet Shiga toxin 10 290 20/60 967
producing E. coli.
FN.200.6 FoodNet Shigella............ 10 234 10/60 390
FN.200.7 FoodNet Vibrio.............. 10 46 10/60 77
FN.200.8 FoodNet Yersinia............ 10 55 10/60 92
FN.200.9 FoodNet Hemolytic Uremic 10 10 1 100
Syndrome.
FN.200.10 FoodNet Clinical Laboratory 10 70 10/60 117
Practices and Testing
Volume.
FSN.300.1 FluSurv-Net Influenza 15 727 25/60 4544
Hospitalization
Surveillance Network Case
Report Form.
FSN.300.2 FluSurv-Net Influenza 14 16 10/60 37
Hospitalization
Surveillance Project
Vaccination Phone Script
and Consent Form (English/
Spanish).
FSN.300.3 FluSurv-Net Influenza 14 126 5/60 147
Hospitalization
Surveillance Project
Provider Vaccination
History Fax Form (Children/
Adults).
FSN.300.4 FluSurv-NET Laboratory 15 16 10/60 40
Survey.
HAIC.400.1 HAIC--Multi-site Gram- 11 1581 29/60 8406
Negative Surveillance
Initiative (MuGSI) Case
Report Form.
HAIC.400.2 HAIC MuGSI CA CP-CRE Health 10 10 30/60 50
interview.
HAIC.400.3 HAIC MuGSI Supplemental 11 1 20/60 4
Surveillance Officer Survey.
HAIC.400.4 HAIC--Invasive 10 788 29/60 3809
Staphylococcus aureus
Infection Case Report Form.
HAIC.400.5 HAIC--Invasive 10 11 9/60 17
Staphylococcus aureus
Laboratory Survey.
HAIC.400.6 HAIC--Invasive 10 1 10.5/60 2
Staphylococcus aureus
Supplemental Surveillance
Officers Survey.
[[Page 14503]]
HAIC.400.7 HAIC--CDI Case Report and 10 1650 38/60 10450
Treatment Form.
HAIC.400.8 HAIC--Annual Survey of 10 16 17/60 45
Laboratory Testing
Practices for C. difficile
Infections.
HAIC.400.9 HAIC--CDI Annual 10 1 15/60 3
Surveillance Officers
Survey.
HAIC.400.10 HAIC--Emerging Infections 10 45 5/60 38
Program C. difficile
Surveillance Nursing Home
Telephone Survey (LTCF).
HAIC.400.11 HAIC Candidemia Case Report 10 170 40/60 1133
Form.
HAIC.400.12 HAIC--Laboratory Testing 10 20 14/60 47
Practices for Candidemia
Questionnaire.
HAIC.400.13 HAIC Death Ascertainment 10 8 1440/60 1,920
Project.
---------------------------------------------------------------
Total................................. .............. ............................ .............. .............. .............. 42,440
--------------------------------------------------------------------------------------------------------------------------------------------------------
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. 2024-03889 Filed 2-26-24; 8:45 am]
BILLING CODE 4163-18-P
