60 Day FRN

33950

Federal Register / Vol. 90, No. 136 / Friday, July 18, 2025 / Notices

company name (if any), and
‘‘Information Collection 3090–0326;
Construction Payrolls and Basic
Records’’ on your attached document. If
your comment cannot be submitted
using https://www.regulations.gov, call
or email the points of contact in the FOR
FURTHER INFORMATION CONTACT section of
this document for alternate instructions.
Instructions: Please submit comments
only and cite Information Collection
3090–0326; Construction Payrolls and
Basic Records, in all correspondence
related to this collection. Comments
received generally will be posted
without change to http://
www.regulations.gov, including any
personal and/or business confidential
information provided. To confirm
receipt of your comment(s), please
check www.regulations.gov,
approximately two-to-three days after
submission to verify posting.
FOR FURTHER INFORMATION CONTACT: Ms.
Johnie McDowell, Senior Procurement
Analyst, GSA, at telephone 202–718–
6112 or via email at [email protected]
for clarification of content.
SUPPLEMENTARY INFORMATION:

khammond on DSK9W7S144PROD with NOTICES

A. Purpose
The Federal Acquisition Regulation
(FAR) Clause 52.222–8 Payrolls and
Basic Records requires United States
construction contracts in excess of
$2,000 to submit weekly for each week
in which any contract work is
performed a copy of all payrolls to the
Contracting Officer. The clause allows
contractors to submit the required
weekly payroll information using the
DOL WH–347 form or any other form
desired. GSA deviated from the FAR
clause to allow these construction
contractors to use an electronic means
to submit the required weekly payroll
data. The proposed revision will
increase the efficiency of the weekly
payroll certification process for the
contractor, GSA and the contractor’s
employee through the use of an
automated process. The current manual
process for reviewing weekly certified
payroll data requires an enormous
amount of labor hours and has a large
probability of human error, i.e. nonidentification or delayed identification
of errors in pay for covered workers.
Delays in identifying payroll errors are
costly to the contractor who will need
to pay retroactive wage adjustments and
the employee will have suffered
reduced economic purchase power due
to the error in wages.

SAM.gov reports for Fiscal Year 2023.
The report indicated 182 construction
contractors for GSA projects were
subject to the Davis-Bacon or Related
Act. GSA’s automation of the data
collection process will not increase the
existing data collection burden from the
DOL Wage and Hour Division (WHD)
the Office of Management and Budget
(OMB) Information Control No. 1235–
0008, Davis-Bacon Certified Payroll or
1235–0018, Records to be kept by
Employers—Fair Labor Standards Act.
Respondents: 182 (170 prime
contractors plus 12 subcontractors).
Responses per Respondent: 52 (1 for
each week of the year).
Total Annual Responses: 9,464 (182
respondents × 52 responses).
Hours per Response: 33 minutes
(weighted average of 56 minutes (DOL
estimated time to input information
plus 1 minute recordkeeping for initial
entry) + 31 minutes (estimated time to
certify payroll in new system plus 1
minute recordkeeping).
Total Burden Hours: 5,205 (9,464
annual responses × 33 minutes) ÷ 60
minutes).
C. Public Comments
Public comments are particularly
invited on: Whether this collection of
information is necessary, whether it will
have practical utility; whether our
estimate of the public burden of this
collection of information is accurate,
and based on valid assumptions and
methodology; ways to enhance the
quality, utility, and clarity of the
information to be collected; and ways in
which we can minimize the burden of
the collection of information on those
who are to respond, through the use of
appropriate technological collection
techniques or other forms of information
technology.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the Regulatory Secretariat Division by
calling 202–501–4755 or emailing
[email protected]. Please cite OMB
Control No. 3090–0326, Construction
Payrolls and Basic Records, in all
correspondence.
William F. Clark,
Director, Office of Government-wide
Acquisition Policy, Office of Acquisition
Policy, Office of Government-wide Policy.

B. Annual Reporting Burden

[FR Doc. 2025–13525 Filed 7–17–25; 8:45 am]

GSA bases the following burden
estimates for certified payrolls on

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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–25–1378; Docket No. CDC–2025–
0124]

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 three-year
extension to a generic information
collection project titled Assessing
Respirator Perceptions, Experiences,
and Maintenance. NIOSH proposes
using surveys, interviews, focus groups,
and physiological monitoring to assess
current perceptions in respirator use as
well as gaps in respirator use,
maintenance, and programs.
DATES: CDC must receive written
comments on or before September 16,
2025.
SUMMARY:

You may submit comments,
identified by Docket No. CDC–2025–
0124 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
or by U.S. mail to the address listed
above.

ADDRESSES:

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

FOR FURTHER INFORMATION CONTACT:

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Federal Register / Vol. 90, No. 136 / Friday, July 18, 2025 / Notices
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
Assessing Respirator Perceptions,
Experiences, and Maintenance (OMB

Control No. 0920–1378, Exp. 11/30/
2025)—Extension—National Institute
for Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC), National Institute for
Occupational Safety and Health
(NIOSH), is requesting approval of a
three-year Extension for the Generic
information collection request (ICR)
titled ‘‘Assessing Respirator
Perceptions, Experiences, and
Maintenance.’’
The National Personal Protective
Technology Laboratory (NPPTL) is a
division of NIOSH. NPPTL was
established in 2001, at the request of
Congress, with the mission of
preventing disease, injury, and death for
the millions of working men and
women relying on personal protective
technology (PPT). As the nation’s
respirator approver for all workplaces
(42 CFR part 84), the development of
NPPTL filled a need for improved
personal protective equipment (PPE)
and focused research into PPT. To this
end, NPPTL conducts respiratory
protection research and leads the
development and revision of test
methods necessary for respirator
approval to prevent exposures to
inhalation hazards, dermal hazards, and
any other hazardous environmental
threats within an occupational setting.
Federal regulations exist regarding the
use of respirators in the workplace. The
Occupational Safety and Health
Administration (OSHA) requires
employers whose hazard management
includes the use of respirators to have
a respiratory protection program, which
has specified components. Thus, the
information collected from human
subjects about their use of respirators is
generally consistent across NPPTL
studies with only the use conditions
changing (e.g., respirator type or
management implementation practices
related to cleaning/decontamination, fit

testing, and training). NPPTL requests a
three-year Extension to its Generic ICR
package for information collected from
individual workers and managers
related to the perceptions, maintenance,
and evaluation of respirator use on the
job.
Different types of data collection
including surveys, focus groups,
interviews, and physiological
monitoring will be used to: (1) assess
workers’ health and safety knowledge,
attitudes, skills, and other attributes as
they relate to their respiratory
protection use and maintenance; (2)
identify and overcome barriers that
workers face while using respiratory
protection to prevent exposure to
contaminants and other hazards; (3)
understand organizations’ maintenance
of respiratory protection programs
(RPP), directives, and guidelines that
support worker best practices; and (4)
determine appropriate training,
interventions, and programs that
support activities around respirator use
and maintenance. Data collection may
focus on respirator types ubiquitous to
the industry being studied, new to the
industry being studied, or novel to any
industry. These data collection efforts
may occur either electronically or in the
field.
Respondents are expected to include
a variety of employees from occupations
such as public safety and emergency
response, healthcare, and social
assistance occupations who wear or
manage respirator use on the job.
Expected respondent job roles include
industrial hygienists, occupational
health professionals, infection control
professionals, physicians, nurse
practitioners, nurses, infection
preventionists, fire department chiefs,
battalion chiefs, sheriffs, shift
supervisors, firefighters, police officers,
and paramedics.
CDC requests OMB approval for an
estimated 13,071 burden hours. There is
no cost to respondents other than their
time to participate.

ESTIMATED ANNUALIZED BURDEN HOURS

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Type of respondents

Industry employees who wear
respirators or oversee respirator use.
Industry employees who wear
respirators or oversee respirator use.
Industry employees who wear
respirators or oversee respirator use.

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Number of
respondents

Form name

Number of
responses per
respondent

Average
burden per
response
(in hours)

Total
burden
(in hours)

Informed consent ..............................................

10,150

1

5/60

846

Perceptions-based survey instrument ..............

3,450

2

15/60

1,725

Knowledge-based survey instrument ...............

2,000

1

30/60

1,000

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Federal Register / Vol. 90, No. 136 / Friday, July 18, 2025 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued

Type of respondents

Number of
respondents

Form name

Industry employees who wear
Interview/Focus group ......................................
respirators or oversee respirator use.
Industry employees who wear a
Physiological Monitoring: Heart rate, blood
respirator as a part of their job.
pressure, blood oxygen saturation, breathing
rate.
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. 2025–13507 Filed 7–17–25; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–25–0666; Docket No. CDC–2025–
0091]

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 National
Healthcare Safety Network (NHSN).
NHSN provides facilities, states,
regions, and the nation with data
necessary to identify problem areas,
measure the progress of prevention
efforts, and ultimately eliminate
healthcare-associated infections (HAIs)
nationwide.

khammond on DSK9W7S144PROD with NOTICES

SUMMARY:

CDC must receive written
comments on or before September 16,
2025.

DATES:

You may submit comments,
identified by Docket No. CDC–2025–
0091 by either of the following methods:

ADDRESSES:

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Total
burden
(in hours)

250

2

1

500

1,000

1

9

9,000

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

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

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

13,071

• 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
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

PO 00000

Average
burden per
response
(in hours)

Number of
responses per
respondent

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
National Healthcare Safety Network
(NHSN) (OMB Control No. 0920–0666,
Exp. 12/31/2027)—Revision—National
Center for Emerging and Zoonotic
Infection Diseases (NCEZID), Centers for
Disease Control and Prevention (CDC)
Background and Brief Description
The Division of Healthcare Quality
Promotion (DHQP), National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC) collects
data from healthcare facilities in the
National Healthcare Safety Network
(NHSN) under OMB Control No. 0920–
0666. NHSN provides facilities, states,
regions, and the nation with data
necessary to identify problem areas,
measure the progress of prevention
efforts, and ultimately eliminate
healthcare-associated infections (HAIs)
nationwide. NHSN allows healthcare
facilities to track blood safety errors and
various healthcare-associated infection
prevention practice methods such as
healthcare personnel influenza vaccine
status and corresponding infection
control adherence rates.

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