Proposed Data Collection Submitted for Public Comment and Recommendations, 87579-87581 [2024-25554]
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lotter on DSK11XQN23PROD with NOTICES1
Federal Register / Vol. 89, No. 213 / Monday, November 4, 2024 / Notices
prosecuting, enforcing, or carrying out a
statute, rule, regulation, or order when
GSA becomes aware of a violation or
potential violation of civil or criminal
law or regulation.
c. To an appeal, grievance, hearing, or
complaints examiner; an equal
employment opportunity investigator,
arbitrator, or mediator; and an exclusive
representative or other person
authorized to investigate or settle a
grievance, complaint, or appeal filed by
an individual who is the subject of the
record.
d. To the Office of Personnel
Management (OPM), the Office of
Management and Budget (OMB), and
the Government Accountability Office
(GAO) in accordance with their
responsibilities for evaluating Federal
programs.
e. To a Member of Congress or his or
her staff on behalf of and at the request
of the individual who is the subject of
the record.
f. To an expert, consultant, or
contractor of GSA in the performance of
a Federal duty to which the information
is relevant.
g. To the National Archives and
Records Administration (NARA) for
records management purposes.
h. In connection with any litigation or
settlement discussions regarding claims
by or against the GSA, including public
filing with a court, to the extent that
GSA determines the disclosure of the
information is relevant and necessary to
the litigation or discussions.
i. To appropriate agencies, entities,
and persons when (1) GSA suspects or
has confirmed that there has been a
breach of the system of records, (2) GSA
has determined that as a result of the
suspected or confirmed breach there is
a risk of harm to individuals, GSA
(including its information systems,
programs, and operations), the Federal
Government, or national security; and
(3) the disclosure made to such
agencies, entities, and persons is
reasonably necessary to assist in
connection with GSA’s efforts to
respond to the suspected or confirmed
breach or to prevent, minimize, or
remedy such harm.
j. To another Federal agency or
Federal entity, when GSA determines
that information from this system of
records is reasonably necessary to assist
the recipient agency or entity in (1)
responding to a suspected or confirmed
breach or (2) preventing, minimizing, or
remedying the risk of harm to
individuals, the recipient agency or
entity (including its information
systems, programs, and operations), the
Federal Government, or national
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87579
security, resulting from a suspected or
confirmed breach.
k. To compare such records to other
agencies’ systems of records or to nonFederal records, in coordination with an
OIG in conducting an audit,
investigation, inspection, evaluation, or
some other review as authorized by the
IG Act.
for application user account
authorization and identity verification
for real property bidders; required use of
GSA SecureAuth for internal GSA users;
and use of encryption for certain data
transfers. Physical security measures are
provided by the hosting service and
ensure that unauthorized access to
physical systems is not permitted.
POLICIES AND PRACTICES FOR STORAGE OF
RECORDS:
RECORD ACCESS PROCEDURES:
Electronic records are stored on a
secure server with access limited to staff
who may access the records only by
means of a lawful government purpose.
Information is encrypted in transit and
at rest.
POLICIES AND PRACTICES FOR RETRIEVAL OF
RECORDS:
Records are retrievable by a personal
identifier or by other appropriate type of
designation approved by GSA.
POLICIES AND PRACTICES FOR RETENTION AND
DISPOSAL OF RECORDS:
Content in this system will be
disposed according to the following
GSA schedule:
121.1/050 Property Disposal Case
Records. This series contains records
related to the process of appraising
federally-owned real property (both
developed and undeveloped), and the
disposal activities associated with
closing, selling, destroying, transferring,
or otherwise removing from the Federal
Government’s real property inventory.
Such records include those used in the
determination of excess real property,
disposal of excess and surplus real
property case files, correspondence, and
related records.
Retention Instructions:
Permanent. Cut off at the end of the
fiscal year following case completion
and fulfillment of all restrictions on the
disposed property. Transfer to NARA 15
years after cutoff.
Legal Disposition Authority: DAA–
0121–2015–0001–0009 (121.1/050).
ADMINISTRATIVE, TECHNICAL, AND PHYSICAL
SAFEGUARDS:
Records in the system are protected
from unauthorized access and misuse
through a combination of administrative
and technical measures. Administrative
measures include but are not limited to
policies that limit system access to
individuals within an agency with a
legitimate business need, and regular
review of security procedures and best
practices to enhance security. Technical
measures include but are not limited to
system design that allows authorized
system users access only to data for
which they are responsible; AWS
security tools; required use of Login.gov
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Frm 00043
Fmt 4703
Sfmt 4703
If an individual wishes to access any
data or record pertaining to him or her
in the system after it has been
submitted, that individual should
consult the GSA’s Privacy Act
implementation rules available at 41
CFR part 105–64.2.
CONTESTING RECORD PROCEDURES:
If an individual wishes to contest the
content of any record pertaining to him
or her in the system after it has been
submitted, that individual should
consult the GSA’s Privacy Act
implementation rules available at 41
CFR part 105–64.4.
NOTIFICATION PROCEDURES:
If an individual wishes to be notified
at his or her request if the system
contains a record pertaining to him or
her after it has been submitted, that
individual should consult the GSA’s
Privacy Act implementation rules
available at 41 CFR part 105–64.4.
EXEMPTIONS PROMULGATED FOR THE SYSTEM:
None.
HISTORY:
None.
Richard Speidel,
Chief Privacy Officer, Office of Enterprise
Data & Privacy Management, General Services
Administration.
[FR Doc. 2024–25577 Filed 11–1–24; 8:45 am]
BILLING CODE 6820–AB–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Toxic Substances and
Disease Registry
[60Day–25–0048; Docket No. ATSDR–2024–
0005]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Agency for Toxic Substances
and Disease Registry (ATSDR),
Department of Health and Human
Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Agency for Toxic
Substances and Disease Registry
SUMMARY:
E:\FR\FM\04NON1.SGM
04NON1
87580
Federal Register / Vol. 89, No. 213 / Monday, November 4, 2024 / Notices
(ATSDR), 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
ATSDR Exposure Investigations (EIs).
ATSDR EIs are deigned to fill data gaps
by conducting environmental and
biological sampling and to evaluate
public health issues at a site resulting
from environmental exposures.
DATES: ATSDR must receive written
comments on or before January 3, 2025.
ADDRESSES: You may submit comments,
identified by Docket No. ATSDR–2024–
0005 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. ATSDR will post,
without change, all relevant comments
to www.regulations.gov.
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.
Please note: Submit all comments through
the Federal eRulemaking portal
(www.regulations.gov) or by U.S. mail to the
address listed above.
Background and Brief Description
The Agency for Toxic Substances and
Disease Registry (ATSDR) is requesting
a three-year Extension of this Generic
Clearance to allow the agency to
conduct Exposure Investigations (EIs),
through methods developed by ATSDR.
After a chemical release or suspected
release into the environment, EIs are
usually requested by officials of a state
health agency, county health
departments, the Environmental
Protection Agency (EPA), the general
public, and ATSDR staff.
EI results are used by public health
professionals, environmental risk
managers, and other decision makers to
determine if current conditions warrant
intervention strategies to minimize or
eliminate human exposure. For
example, an EI that ATSDR previously
conducted during included
environmental sampling to evaluate
non-drinking water exposure to per- and
polyfluoroalkyl substances (PFAS) in
two communities that were shown to be
exposed to PFAS in their drinking
water.
During the most recent clearance
period (4/30/2022–present) a single
Generic Exposure Investigation
information collection request (ICR) was
submitted. The EI conducted under this
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
lotter on DSK11XQN23PROD with NOTICES1
FOR FURTHER INFORMATION CONTACT:
VerDate Sep<11>2014
17:28 Nov 01, 2024
Jkt 265001
Proposed Project
ATSDR Exposure Investigations (EIs)
(OMB Control No. 0923–0048, Exp. 6/
30/2025)—Extension—Agency for Toxic
Substances and Disease Registry
(ATSDR).
PO 00000
Frm 00044
Fmt 4703
Sfmt 4703
clearance period was an EI in Jasper and
Newton Counties, Missouri to evaluate
exposure to lead in a former mining
community. ATSDR collected blood
samples from community members most
vulnerable to the impacts of lead
exposure: children five years old and
younger along with pregnant women
and women of childbearing age. ATSDR
partnered with the U.S. Environmental
Protection Agency (EPA) and the
Missouri Department of Health and
Senior Services (MDHSS) who collected
environmental samples, including soil,
dust wipes, drinking water and paint,
along with the results of the blood
sampling. Appropriate EI procedures,
including use of consent forms and
questionnaires were used in the EI. The
environmental sampling was submitted
under this OMB Control Number with a
burden of 426 hours.
All of ATSDR’s targeted biological
assessments (e.g., urine, blood) and
some of the environmental
investigations (e.g., air, water, soil, dust,
or food sampling) involve participants
to determine whether they are or have
been exposed to unusual levels of
pollutants at specific locations (e.g.,
where people live, spend leisure time,
or anywhere they might come into
contact with contaminants under
investigation). Questionnaires,
appropriate to the specific contaminant,
are generally needed in about half of the
EIs (at most approximately 12 per year)
to assist in interpreting the biological or
environmental sampling results. ATSDR
collects contact information (e.g., name,
address, phone number) to provide the
participant with their individual results.
ATSDR also collects information on
other possible confounding sources of
chemical(s) exposure such as medicines
taken, foods eaten, hobbies, jobs, etc. In
addition, ATSDR asks questions on
recreational or occupational activities
that could increase a participant’s
exposure potential. That information
represents an individual’s exposure
history.
The number of questions can vary
depending on the number of chemicals
being investigated, the route of exposure
(e.g., breathing, eating, touching), and
number of other sources of the
chemical(s) (e.g., products used, jobs).
We use approximately 12–20 questions
about the pertinent environmental
exposures per investigation. A question
bank is available for health assessors to
use as a basis of questions to be asked
during the EI, but EI-specific questions
may be included as appropriate.
Typically, the number of participants in
an individual EI ranges from 10 to 100.
Participation is completely voluntary,
and there are no costs to participants
E:\FR\FM\04NON1.SGM
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87581
Federal Register / Vol. 89, No. 213 / Monday, November 4, 2024 / Notices
other than their time. Based on a
maximum of 12 EIs per year and 100
participants each, the estimated
annualized burden hours are 600.
ESTIMATED ANNUALIZED BURDEN HOURS
Total burden
(in hours)
Form name
Exposure Investigation Participants ..
Chemical Exposure Questions .........
1,200
1
30/60
600
Total ...........................................
...........................................................
........................
........................
........................
600
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
[60Day–25–1424; Docket No. CDC–2024–
0087]
You may submit comments,
identified by Docket No. CDC–2024–
0087 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.
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Please note: Submit all comments through
the Federal eRulemaking portal
(www.regulations.gov) or by U.S. mail to the
address listed above.
[FR Doc. 2024–25554 Filed 11–1–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
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 U.S. National
Authority for Containment of Poliovirus
Data Collection Tools. Data collection
will capture information relating to a
poliovirus containment breach or
incident at a U.S. facility and will assist
the U.S. National Authority for
Containment of Poliovirus (U.S. NAC)
in the initial stages of the investigation
into the breach, and also gather
information regarding personal
protective equipment and practices used
for work and/or storage of infectious
materials or potentially infectious at
laboratory facilities.
DATES: CDC must receive written
comments on or before January 3, 2025.
SUMMARY:
lotter on DSK11XQN23PROD with NOTICES1
Average
burden per
response
(in hours)
Number of
responses per
respondent
Number of
respondents
Type of respondents
VerDate Sep<11>2014
17:28 Nov 01, 2024
Jkt 265001
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
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:
FOR FURTHER INFORMATION CONTACT:
PO 00000
Frm 00045
Fmt 4703
Sfmt 4703
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
U.S. National Authority for
Containment of Poliovirus Data
Collection Tools (OMB Control No.
0920–1424, Exp. 12/31/2026)—
Revision—Office of Readiness and
Response (ORR), Centers for Disease
Control and Prevention CDC)
Background and Brief Description
The role of the National Authority for
Containment of Poliovirus (U.S. NAC) is
to ensure that the requirements
established in the World Health
Organization (WHO) Global Action Plan
(GAP) III/IV standard are effectively
implemented and maintained in
facilities working with or storing
infectious poliovirus or potentially
infectious materials.
Risk assessments following an
incident are a critical component for
adequate application of the GAP
standard. To support risk assessment
activities, The Facility Incident
Reporting Form for Poliovirus Release
and Potential Exposure and the Facility
Incident Reporting Form for Poliovirus
Theft or Loss was created for facilities
to capture and submit incident
E:\FR\FM\04NON1.SGM
04NON1
]]>Agencies
[Federal Register Volume 89, Number 213 (Monday, November 4, 2024)]
[Notices]
[Pages 87579-87581]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-25554]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Toxic Substances and Disease Registry
[60Day-25-0048; Docket No. ATSDR-2024-0005]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Agency for Toxic Substances and Disease Registry (ATSDR),
Department of Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Agency for Toxic Substances and Disease Registry
[[Page 87580]]
(ATSDR), 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 ATSDR Exposure Investigations
(EIs). ATSDR EIs are deigned to fill data gaps by conducting
environmental and biological sampling and to evaluate public health
issues at a site resulting from environmental exposures.
DATES: ATSDR must receive written comments on or before January 3,
2025.
ADDRESSES: You may submit comments, identified by Docket No. ATSDR-
2024-0005 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. ATSDR 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;
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
ATSDR Exposure Investigations (EIs) (OMB Control No. 0923-0048,
Exp. 6/30/2025)--Extension--Agency for Toxic Substances and Disease
Registry (ATSDR).
Background and Brief Description
The Agency for Toxic Substances and Disease Registry (ATSDR) is
requesting a three-year Extension of this Generic Clearance to allow
the agency to conduct Exposure Investigations (EIs), through methods
developed by ATSDR. After a chemical release or suspected release into
the environment, EIs are usually requested by officials of a state
health agency, county health departments, the Environmental Protection
Agency (EPA), the general public, and ATSDR staff.
EI results are used by public health professionals, environmental
risk managers, and other decision makers to determine if current
conditions warrant intervention strategies to minimize or eliminate
human exposure. For example, an EI that ATSDR previously conducted
during included environmental sampling to evaluate non-drinking water
exposure to per- and polyfluoroalkyl substances (PFAS) in two
communities that were shown to be exposed to PFAS in their drinking
water.
During the most recent clearance period (4/30/2022-present) a
single Generic Exposure Investigation information collection request
(ICR) was submitted. The EI conducted under this clearance period was
an EI in Jasper and Newton Counties, Missouri to evaluate exposure to
lead in a former mining community. ATSDR collected blood samples from
community members most vulnerable to the impacts of lead exposure:
children five years old and younger along with pregnant women and women
of childbearing age. ATSDR partnered with the U.S. Environmental
Protection Agency (EPA) and the Missouri Department of Health and
Senior Services (MDHSS) who collected environmental samples, including
soil, dust wipes, drinking water and paint, along with the results of
the blood sampling. Appropriate EI procedures, including use of consent
forms and questionnaires were used in the EI. The environmental
sampling was submitted under this OMB Control Number with a burden of
426 hours.
All of ATSDR's targeted biological assessments (e.g., urine, blood)
and some of the environmental investigations (e.g., air, water, soil,
dust, or food sampling) involve participants to determine whether they
are or have been exposed to unusual levels of pollutants at specific
locations (e.g., where people live, spend leisure time, or anywhere
they might come into contact with contaminants under investigation).
Questionnaires, appropriate to the specific contaminant, are generally
needed in about half of the EIs (at most approximately 12 per year) to
assist in interpreting the biological or environmental sampling
results. ATSDR collects contact information (e.g., name, address, phone
number) to provide the participant with their individual results. ATSDR
also collects information on other possible confounding sources of
chemical(s) exposure such as medicines taken, foods eaten, hobbies,
jobs, etc. In addition, ATSDR asks questions on recreational or
occupational activities that could increase a participant's exposure
potential. That information represents an individual's exposure
history.
The number of questions can vary depending on the number of
chemicals being investigated, the route of exposure (e.g., breathing,
eating, touching), and number of other sources of the chemical(s)
(e.g., products used, jobs). We use approximately 12-20 questions about
the pertinent environmental exposures per investigation. A question
bank is available for health assessors to use as a basis of questions
to be asked during the EI, but EI-specific questions may be included as
appropriate. Typically, the number of participants in an individual EI
ranges from 10 to 100. Participation is completely voluntary, and there
are no costs to participants
[[Page 87581]]
other than their time. Based on a maximum of 12 EIs per year and 100
participants each, the estimated annualized burden hours are 600.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondents Form name respondents responses per response (in (in hours)
respondent hours)
----------------------------------------------------------------------------------------------------------------
Exposure Investigation Chemical 1,200 1 30/60 600
Participants. Exposure
Questions.
---------------------------------------------------------------------------------
Total..................... ................ .............. .............. .............. 600
----------------------------------------------------------------------------------------------------------------
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. 2024-25554 Filed 11-1-24; 8:45 am]
BILLING CODE 4163-18-P
