60 Day FRN

Att. 2-Federal Register 60day FRN.pdf

[NCEZID] Emerging Infections Program

60 Day FRN

OMB: 0920-0978

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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

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SUMMARY:

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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:

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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

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HAIC.400.2
HAIC.400.3
HAIC.400.4
HAIC.400.5
HAIC.400.6

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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

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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

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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).

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