60d FRN - published

25299

Federal Register / Vol. 90, No. 114 / Monday, June 16, 2025 / Notices
The burden hours are estimated based
on limited pilot testing conducted
internally using the survey instrument.
In these pilot tests, the amount of time
for instruction review, collection of
mock information, and the survey
completion was between 2–4 minutes.
The median time of three minutes was
used to estimate annual burden hours.
Currently, the total number of clinics
which will be using this system in the

United States is unknown. However, the
total number of employed miners in the
metal/non-metal industry is known,
with 255,702 employed in 2023. MSHA
estimated in their regulatory documents
that anywhere between 25%–75% of
metal/non-metal miners will participate
in this program, leading to an annual
average number of radiographs
submitted to be 13,500. If we take the
total number of clinics to be at least

double the number of clinics offering
NIOSH-approved radiography listed on
NIOSH’s website (169), then at least 338
clinics will participate.
CDC requests OMB approval for three
years, with an estimated 462 annual
burden hours. There are no costs to
respondents other than their time to
participate.

ESTIMATED ANNUALIZED BURDEN HOURS
Form name

Clinics and staff ................................

Request to Access X-ray Classification Submission.
X-ray classification submission for
metal and non-metal miners.

Clinics and staff ................................
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. 2025–10899 Filed 6–13–25; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–25–1432; Docket No. CDC–2025–
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 continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled NCEZID Rapid
Message Testing & Development
System. This program will enable the
National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID)
to test health messages and gather

ddrumheller on DSK120RN23PROD with NOTICES1

SUMMARY:

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18:38 Jun 13, 2025

Jkt 265001

Number of
responses per
respondent

Number of
respondents

Type of respondents

Frm 00099

Fmt 4703

Total burden
(in hours)

338

1

1/60

6

338

40

2/60

451

........................

........................

........................

462

information to inform the development
of health messages.
DATES: CDC must receive written
comments on or before August 15, 2025.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2025–
0012 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: 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

PO 00000

Average
burden per
response
(in hours)

Sfmt 4703

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
NCEZID Rapid Message Testing &
Development System (OMB Control No.

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25300

Federal Register / Vol. 90, No. 114 / Monday, June 16, 2025 / Notices

0920–1432, Exp. 5/31/2025)—
Extension—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
CDC’s National Center for Emerging
and Zoonotic Infectious Diseases
(NCEZID) offers numerous powerful
resources to anticipate, prevent, and
address outbreaks of infectious diseases.
From researchers to emergency
responders; from laboratories to
surveillance of mobile populations;
from collaborations at the Federal level
to partnerships at the local level,
NCEZID keeps people safe from threats
like anthrax, Ebola virus, Zika virus,
sepsis, mpox, and foodborne illnesses
like Salmonella. These efforts are vital
to protect and save lives.

the Center, prior to the dissemination of
those messages and associated
communications materials. The data
collection is intended to ensure NCEZID
messages are clear, salient, appealing,
and persuasive to target audiences. Data
will guide revisions to existing or draft
messages, inform the development of
new messages, and otherwise enable
message developers to make optimal
decisions about message content,
format, and dissemination so that
NCEZID’s messages effectively reach
and resonate with their intended
audiences.
Data collection methods proposed for
this system include in-depth interviews,
online or in-person focus groups, and
online surveys. CDC requests OMB
approval for an estimated 3,431 annual
burden hours. There is no cost to
respondents other than their time.

The ability to effectively
communicate with the public about
these threats is one of NCEZID’s most
vital roles. Particularly during an
outbreak, it is critical that the public
understands what is happening and
why, and trusts and follows public
health leaders’ guidance. Recent public
health responses to COVID–19 and
mpox have underscored the need to
improve the speed and content of health
communications, particularly among
populations at higher risk for zoonotic
and infectious diseases. This Rapid
Message Testing & Message
Development System enables NCEZID to
collect information vital to the
development of clear, salient, relevant,
appealing, and persuasive messages
related to outbreaks and other emerging
and zoonotic diseases. The system also
allows for the relatively rapid testing of
messages when the need arises within

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent

Average
burden per
response
(in hr)

Total burden
(in hr)

Form name

General public ...................................
General public ...................................

10,000
2,880

1
1

10/60
5/60

1,667
240

3,600

1

5/60

300

General public ...................................
Healthcare and specialty audiences
Healthcare and specialty audiences

Surveys Question Bank ...................
Screening and Recruitment Question Bank.
Screening and Recruitment Question Bank.
Focus Groups Question Bank ..........
Focus Groups Question Bank ..........
In-Depth Interviews Question Bank

288
288
72

1
1
1

2
2
1

576
576
72

Total ...........................................

...........................................................

........................

........................

........................

3,431

Healthcare and specialty audiences

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. 2025–10907 Filed 6–13–25; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–25–1317; Docket No. CDC–2025–
0023]

ddrumheller on DSK120RN23PROD with NOTICES1

Number of
respondents

Type of respondent

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

SUMMARY:

VerDate Sep<11>2014

18:38 Jun 13, 2025

Jkt 265001

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 National
Healthcare Safety Network (NHSN)
Respiratory Data. This data collection is
designed to standardize the data
elements collected across the country
regarding the impact of respiratory
viruses on healthcare facilities.
DATES: CDC must receive written
comments on or before August 15, 2025.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2025–
0023 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

PO 00000

Frm 00100

Fmt 4703

Sfmt 4703

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: 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

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16JNN1