Pesticide Registration Review; Proposed Interim Decision and Draft Risk Assessment Addendum for Ethylene Oxide; Notice of Availability, 22447-22449 [2023-07727]
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[FR Doc. 2023–07806 Filed 4–12–23; 8:45 am]
BILLING CODE 6717–01–P
DEPARTMENT OF ENERGY
Federal Energy Regulatory
Commission
Combined Notice of Filings
Take notice that the Commission has
received the following Natural Gas & Oil
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lotter on DSK11XQN23PROD with NOTICES1
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time on the specified comment date.
The filings are accessible in the
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fercgensearch.asp) by querying the
docket number.
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docs-filing/efiling/filing-req.pdf. For
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Dated: April 7, 2023.
Debbie-Anne A. Reese,
Deputy Secretary.
[FR Doc. 2023–07777 Filed 4–12–23; 8:45 am]
BILLING CODE 6717–01–P
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ENVIRONMENTAL PROTECTION
AGENCY
[FRL–10855–01–OMS]
Cross-Media Electronic Reporting:
Authorized Program Revision
Approval, New Jersey Department of
Environmental Protection (NJDEP)
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
This notice announces the
Environmental Protection Agency’s
(EPA) approval of the New Jersey
Department of Environmental Protection
(NJDEP) request to revise/modify certain
of its EPA-authorized programs to allow
electronic reporting.
DATES: EPA approves the authorized
program revisions/modifications as of
April 13, 2023.
FOR FURTHER INFORMATION CONTACT:
Shirley M. Miller, U.S. Environmental
Protection Agency, Office of Information
Management, Mail Stop 2824T, 1200
Pennsylvania Avenue NW, Washington,
DC 20460, (202) 566–2908,
miller.shirley@epa.gov.
SUPPLEMENTARY INFORMATION: On
October 13, 2005, the final Cross-Media
Electronic Reporting Rule (CROMERR)
was published in the Federal Register
(70 FR 59848) and codified as part 3 of
title 40 of the CFR. CROMERR
establishes electronic reporting as an
acceptable regulatory alternative to
paper reporting and establishes
requirements to assure that electronic
documents are as legally dependable as
their paper counterparts. Subpart D of
CROMERR requires that state, tribal or
local government agencies that receive,
or wish to begin receiving, electronic
reports under their EPA-authorized
programs must apply to EPA for a
revision or modification of those
programs and obtain EPA approval.
Subpart D provides standards for such
approvals based on consideration of the
electronic document receiving systems
that the state, tribe, or local government
will use to implement the electronic
reporting. Additionally, § 3.1000(b)
through (e) of 40 CFR part 3, subpart D
provides special procedures for program
revisions and modifications to allow
electronic reporting, to be used at the
option of the state, tribe or local
government in place of procedures
available under existing programspecific authorization regulations. An
application submitted under the subpart
D procedures must show that the state,
tribe or local government has sufficient
legal authority to implement the
electronic reporting components of the
SUMMARY:
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22447
programs covered by the application
and will use electronic document
receiving systems that meet the
applicable subpart D requirements.
On March 13, 2023, the New Jersey
Department of Environmental Protection
(NJDEP) submitted an application titled
National Pollutant Discharge
Elimination System (NPDES) Electronic
Reporting Tool (NeT) for revisions/
modifications to its EPA-approved
programs under title 40 CFR to allow
new electronic reporting. EPA reviewed
NJDEP’s request to revise/modify its
EPA-authorized programs and, based on
this review, EPA determined that the
application met the standards for
approval of authorized program
revisions/modifications set out in 40
CFR part 3, subpart D. In accordance
with 40 CFR 3.1000(d), this notice of
EPA’s decision to approve NJDEP’s
request to revise/modify its following
EPA-authorized programs to allow
electronic reporting under 40 CFR is
being published in the Federal Register:
Part 123: EPA-Administered Permit
Programs: the National Pollutant
Discharge Elimination System (NPDES)
Reporting under 40 CFR 122 and 125.
NJDEP was notified of EPA’s
determination to approve its application
with respect to the authorized programs
listed above.
Dated: April 6, 2023.
Jennifer Campbell,
Director, Office of Information Management.
[FR Doc. 2023–07725 Filed 4–12–23; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2013–0244; FRL–10818–01–
OCSPP]
Pesticide Registration Review;
Proposed Interim Decision and Draft
Risk Assessment Addendum for
Ethylene Oxide; Notice of Availability
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
This notice announces the
availability of and solicits public
comment on EPA’s proposed interim
registration review decision and draft
risk assessment addendum for ethylene
oxide.
DATES: Comments must be received on
or before June 12, 2023.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPP–2013–0244,
through the Federal eRulemaking Portal
at https://www.regulations.gov. Follow
SUMMARY:
E:\FR\FM\13APN1.SGM
13APN1
22448
Federal Register / Vol. 88, No. 71 / Thursday, April 13, 2023 / Notices
the online instructions for submitting
comments. Do not submit electronically
any information you consider to be
Confidential Business Information (CBI)
or other information whose disclosure is
restricted by statute. Additional
instructions on commenting and visiting
the docket, along with more information
about dockets generally, is available at
https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: The
Chemical Review Manager for ethylene
oxide as listed in table 1.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
This action is directed to the public
in general and may be of interest to a
wide range of stakeholders including
environmental and human health
advocates; distributors and users of
medical devices; owners and operators
of commercial sterilization facilities; the
chemical industry; pesticide users; and
members of the public interested in the
sale, distribution, or use of pesticides.
Since others also may be interested, the
Agency has not attempted to describe all
the specific entities that may be affected
by this action. If you have any questions
regarding the applicability of this action
to a particular entity, consult the
Chemical Review Manager for ethylene
oxide identified in table 1 in unit IV.
B. What should I consider as I prepare
my comments for EPA?
1. Submitting CBI. Do not submit this
information to EPA through
regulations.gov or email. Clearly mark
the part or all of the information that
you claim to be CBI. For CBI
information on a disk or CD–ROM that
you mail to EPA, mark the outside of the
disk or CD–ROM as CBI and then
identify electronically within the disk or
CD–ROM the specific information that
is claimed as CBI. In addition to one
complete version of the comment that
includes information claimed as CBI, a
copy of the comment that does not
contain the information claimed as CBI
must be submitted for inclusion in the
public docket. Information so marked
will not be disclosed except in
accordance with procedures set forth in
40 CFR part 2.
2. Tips for preparing your comments.
When preparing and submitting your
comments, see the commenting tips at:
https://www.epa.gov/dockets/
commenting-epa-dockets.
3. Environmental justice. EPA seeks to
achieve environmental justice, the fair
treatment and meaningful involvement
of any group, including minority and/or
low-income populations, in the
development, implementation, and
enforcement of environmental laws,
regulations, and policies. To help
address potential environmental justice
issues, the Agency seeks information on
any groups or segments of the
population who, as a result of their
location, cultural practices, or other
factors, may have atypical or
disproportionately high and adverse
human health impacts or environmental
effects from exposure to ethylene oxide
(EtO) discussed in this document,
compared to the general population.
health or the environment. As part of
the registration review process, the
Agency has completed a proposed
interim decision and draft risk
assessment addendum for ethylene
oxide (table 1). Through this program,
EPA is ensuring that each pesticide’s
registration is based on current
scientific and other knowledge,
including its effects on human health
and the environment.
II. Background
IV. What action is the Agency taking?
Registration review is EPA’s periodic
review of pesticide registrations to
ensure that each pesticide continues to
satisfy the statutory standard for
registration, that is, the pesticide can
perform its intended function without
unreasonable adverse effects on human
Pursuant to 40 CFR 155.58, this notice
announces the availability of EPA’s
proposed interim registration review
decisions for ethylene oxide and the
draft risk assessment addendum and
opens a 60-day public comment period
on these documents.
III. Authority
EPA is conducting its registration
review of ethylene oxide pursuant to
section 3(g) of the Federal Insecticide,
Fungicide, and Rodenticide Act (FIFRA)
and the Procedural Regulations for
Registration Review at 40 CFR part 155,
subpart C. Section 3(g) of FIFRA
provides, among other things, that the
registrations of pesticides are to be
reviewed every 15 years. Under FIFRA,
a pesticide product may be registered or
remain registered only if it meets the
statutory standard for registration given
in FIFRA section 3(c)(5) (7 U.S.C.
136a(c)(5)). When used in accordance
with widespread and commonly
recognized practice, the pesticide
product must perform its intended
function without unreasonable adverse
effects on the environment; that is,
without any unreasonable risk to man or
the environment, or a human dietary
risk from residues that result from the
use of a pesticide in or on food.
lotter on DSK11XQN23PROD with NOTICES1
TABLE 1—ETHYLENE OXIDE REGISTRATION REVIEW DOCKET DETAILS
Registration review case name and No.
Docket ID No.
Chemical review manager and
contact information
Ethylene oxide Case Number 2275 ..................
EPA–HQ–OPP–2013–0244 .............................
Jessica Bailey OPPethyleneoxideinquiries@
epa.gov.
The registration review docket for a
pesticide includes earlier documents
related to the registration review case.
For example, the review opened with a
Preliminary Work Plan, for public
comment. A Final Work Plan was
placed in the docket following public
comment on the Preliminary Work Plan.
The documents in the docket describe
EPA’s rationales for conducting
additional risk assessments for the
registration review of ethylene oxide, as
well as the Agency’s subsequent risk
findings and consideration of possible
risk mitigation measures. The proposed
interim registration review decision is
supported by the rationale included in
those documents. Following public
comment, the Agency will issue an
interim or final registration review
decision for ethylene oxide.
The registration review final rule at 40
CFR 155.58(a) provides for a minimum
60-day public comment period on all
proposed interim registration review
decisions. This comment period is
intended to provide an opportunity for
public input and a mechanism for
initiating any necessary amendments to
the proposed interim decision. All
comments should be submitted using
the methods in ADDRESSES and must be
received by EPA on or before the closing
date. These comments will become part
of the docket for ethylene oxide.
Comments received after the close of the
comment period will be marked ‘‘late.’’
EPA is not required to consider these
late comments.
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Federal Register / Vol. 88, No. 71 / Thursday, April 13, 2023 / Notices
The Agency will carefully consider all
comments received by the closing date
and may provide a ‘‘Response to
Comments Memorandum’’ in the
docket. The interim registration review
decision will explain the effect that any
comments had on the interim decision
and provide the Agency’s response to
significant comments.
Background on the registration review
program is provided at: https://
www.epa.gov/pesticide-reevaluation.
Authority: 7 U.S.C. 136 et seq.
Dated: March 28, 2023.
Anita Pease,
Director, Antimicrobials Division, Office of
Pesticide Programs.
[FR Doc. 2023–07727 Filed 4–12–23; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–10881–01–OA]
Local Government Advisory
Committee (LGAC) and Small
Communities Advisory Subcommittee
(SCAS) Meeting
Environmental Protection
Agency (EPA).
ACTION: Notification of public meeting.
AGENCY:
Pursuant to the Federal
Advisory Committee Act (FACA), EPA
herby provides notice of a meeting for
the Local Government Advisory
Committee (LGAC) and its Small
Communities Advisory Subcommittee
(SCAS) on the date and time described
below. This meeting will be open to the
public. For information on public
attendance and participation, please see
the registration information under
DATES: The LGAC will have a hybrid
meeting on May 22nd 2023, from 1 to
5 p.m. Eastern Daylight Time and May
23rd, 2023 from 8:30 a.m. to 12 p.m.
Eastern Daylight Time. The SCAS will
have a hybrid meeting prior to the
LGAC on May 22nd, 2023, from 10:30
a.m. to 12 p.m. Eastern Daylight Time.
FOR FURTHER INFORMATION CONTACT:
Paige Lieberman, Designated Federal
Officer (DFO), at LGAC@epa.gov or 202–
564–9957.
Information on Accessibility: For
information on access or services for
individuals requiring accessibility
accommodations, please contact Paige
Lieberman by email at LGAC@epa.gov.
To request accommodation, please do so
five (5) business days prior to the
meeting, to give EPA as much time as
possible to process your request.
SUPPLEMENTARY INFORMATION:
lotter on DSK11XQN23PROD with NOTICES1
SUMMARY:
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17:56 Apr 12, 2023
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Content
The LGAC will discuss several
priority issues at EPA, including
providing draft recommendations on
proposed national drinking water
quality standards for PFAS, continuing
discussions on climate mitigation,
environmental justice and risk
communications regarding PFAS. The
SCAS will review these issues, as well
as discuss recommendations on land
use and transportation issues for small
communities. Both the LGAC and SCAS
will hear from EPA leadership regarding
several new proposed charges. Details
on the charges will be posted online
(link below) one week prior to the
meeting.
Registration
The meeting will be held virtually as
well as in person. Members of the
public who wish to participate should
register by contacting the Designated
Federal Officer (DFO) at LGAC@epa.gov
by May 19, 2023. Online participation
will be via Microsoft Teams. In person
participation will be at EPA
Headquarters, 1200 Constitution Ave.
NW, Washington, DC.
Once available, the agenda and other
supportive meeting materials will be
available online at https://www.epa.gov/
ocir/local-government-advisorycommittee-lgac and will be emailed to
all registered. In the event of
cancellation for unforeseen
circumstances, please contact the DFO
or check the website above for
reschedule information.
Dated: April 3, 2023.
Paige Lieberman,
Designated Federal Officer, U.S.
Environmental Protection Agency.
[FR Doc. 2023–07758 Filed 4–12–23; 8:45 am]
BILLING CODE 6560–50–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality; Notice of Meetings
Agency for Healthcare Research
and Quality (AHRQ), Department of
Health and Human Services (HHS).
ACTION: Notice of Five AHRQ
Subcommittee Meetings.
AGENCY:
The subcommittees listed
below are part of AHRQ’s Health
Services Research Initial Review Group
(IRG) Committee. Grant applications are
to be reviewed and discussed at these
meetings. Each subcommittee meeting
will be closed to the public.
DATES: See below for dates of meetings:
SUMMARY:
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22449
1. Healthcare Research Training (HCRT)
Date: May 18–19, 2023
July 14, 2023
2. Healthcare Safety and Quality
Improvement Research (HSQR)
Date: The date of the HSQR meeting
is yet to be determined and will be
published in an upcoming notice.
3. Healthcare Information Technology
Research (HITR)
Date: June 1–2, 2023
4. Healthcare Effectiveness and
Outcomes Research (HEOR)
Date: June 7–8, 2023
5. Health System and Value Research
(HSVR)
Date: June 15–16, 2023
ADDRESSES: Agency for Healthcare
Research and Quality (Virtual Review
for HCRT, HEOR & HSVR) 5600 Fishers
Lane, Rockville, Maryland 20857, and
Bethesda North Marriott Hotel &
Conference Center (HITR in person
review), 5701 Marinelli Road, Rockville,
MD 20852–2785.
FOR FURTHER INFORMATION CONTACT: (to
obtain a roster of members, agenda or
minutes of the non-confidential portions
of the meetings.)
Jenny Griffith, Committee
Management Officer, Office of
Extramural Research Education and
Priority Populations, Agency for
Healthcare Research and Quality
(AHRQ), 5600 Fishers Lane, Rockville,
Maryland 20857, Telephone (301) 427–
1557.
SUPPLEMENTARY INFORMATION: In
accordance with section 10 (a)(2) of the
Federal Advisory Committee Act (5
U.S.C. App. 2), AHRQ announces
meetings of the above-listed scientific
peer review groups, which are
subcommittees of AHRQ’s Health
Services Research Initial Review Group
Committee. The subcommittee meetings
will be closed to the public in
accordance with the provisions set forth
in 5 U.S.C. App. 2 section 10(d), 5
U.S.C. 552b(c)(4), and 5 U.S.C.
552b(c)(6). The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Agenda items for these meetings are
subject to change as priorities dictate.
Dated: April 7, 2023.
Marquita Cullom,
Associate Director.
[FR Doc. 2023–07747 Filed 4–12–23; 8:45 am]
BILLING CODE 4160–90–P
E:\FR\FM\13APN1.SGM
13APN1
Agencies
[Federal Register Volume 88, Number 71 (Thursday, April 13, 2023)]
[Notices]
[Pages 22447-22449]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-07727]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2013-0244; FRL-10818-01-OCSPP]
Pesticide Registration Review; Proposed Interim Decision and
Draft Risk Assessment Addendum for Ethylene Oxide; Notice of
Availability
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the availability of and solicits public
comment on EPA's proposed interim registration review decision and
draft risk assessment addendum for ethylene oxide.
DATES: Comments must be received on or before June 12, 2023.
ADDRESSES: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPP-2013-0244, through the Federal eRulemaking
Portal at https://www.regulations.gov. Follow
[[Page 22448]]
the online instructions for submitting comments. Do not submit
electronically any information you consider to be Confidential Business
Information (CBI) or other information whose disclosure is restricted
by statute. Additional instructions on commenting and visiting the
docket, along with more information about dockets generally, is
available at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: The Chemical Review Manager for
ethylene oxide as listed in table 1.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
This action is directed to the public in general and may be of
interest to a wide range of stakeholders including environmental and
human health advocates; distributors and users of medical devices;
owners and operators of commercial sterilization facilities; the
chemical industry; pesticide users; and members of the public
interested in the sale, distribution, or use of pesticides. Since
others also may be interested, the Agency has not attempted to describe
all the specific entities that may be affected by this action. If you
have any questions regarding the applicability of this action to a
particular entity, consult the Chemical Review Manager for ethylene
oxide identified in table 1 in unit IV.
B. What should I consider as I prepare my comments for EPA?
1. Submitting CBI. Do not submit this information to EPA through
regulations.gov or email. Clearly mark the part or all of the
information that you claim to be CBI. For CBI information on a disk or
CD-ROM that you mail to EPA, mark the outside of the disk or CD-ROM as
CBI and then identify electronically within the disk or CD-ROM the
specific information that is claimed as CBI. In addition to one
complete version of the comment that includes information claimed as
CBI, a copy of the comment that does not contain the information
claimed as CBI must be submitted for inclusion in the public docket.
Information so marked will not be disclosed except in accordance with
procedures set forth in 40 CFR part 2.
2. Tips for preparing your comments. When preparing and submitting
your comments, see the commenting tips at: https://www.epa.gov/dockets/commenting-epa-dockets.
3. Environmental justice. EPA seeks to achieve environmental
justice, the fair treatment and meaningful involvement of any group,
including minority and/or low-income populations, in the development,
implementation, and enforcement of environmental laws, regulations, and
policies. To help address potential environmental justice issues, the
Agency seeks information on any groups or segments of the population
who, as a result of their location, cultural practices, or other
factors, may have atypical or disproportionately high and adverse human
health impacts or environmental effects from exposure to ethylene oxide
(EtO) discussed in this document, compared to the general population.
II. Background
Registration review is EPA's periodic review of pesticide
registrations to ensure that each pesticide continues to satisfy the
statutory standard for registration, that is, the pesticide can perform
its intended function without unreasonable adverse effects on human
health or the environment. As part of the registration review process,
the Agency has completed a proposed interim decision and draft risk
assessment addendum for ethylene oxide (table 1). Through this program,
EPA is ensuring that each pesticide's registration is based on current
scientific and other knowledge, including its effects on human health
and the environment.
III. Authority
EPA is conducting its registration review of ethylene oxide
pursuant to section 3(g) of the Federal Insecticide, Fungicide, and
Rodenticide Act (FIFRA) and the Procedural Regulations for Registration
Review at 40 CFR part 155, subpart C. Section 3(g) of FIFRA provides,
among other things, that the registrations of pesticides are to be
reviewed every 15 years. Under FIFRA, a pesticide product may be
registered or remain registered only if it meets the statutory standard
for registration given in FIFRA section 3(c)(5) (7 U.S.C. 136a(c)(5)).
When used in accordance with widespread and commonly recognized
practice, the pesticide product must perform its intended function
without unreasonable adverse effects on the environment; that is,
without any unreasonable risk to man or the environment, or a human
dietary risk from residues that result from the use of a pesticide in
or on food.
IV. What action is the Agency taking?
Pursuant to 40 CFR 155.58, this notice announces the availability
of EPA's proposed interim registration review decisions for ethylene
oxide and the draft risk assessment addendum and opens a 60-day public
comment period on these documents.
Table 1--Ethylene Oxide Registration Review Docket Details
------------------------------------------------------------------------
Chemical review
Registration review case name manager and
and No. Docket ID No. contact
information
------------------------------------------------------------------------
Ethylene oxide Case Number 2275. EPA-HQ-OPP-2013-02 Jessica Bailey
44. [email protected].
------------------------------------------------------------------------
The registration review docket for a pesticide includes earlier
documents related to the registration review case. For example, the
review opened with a Preliminary Work Plan, for public comment. A Final
Work Plan was placed in the docket following public comment on the
Preliminary Work Plan.
The documents in the docket describe EPA's rationales for
conducting additional risk assessments for the registration review of
ethylene oxide, as well as the Agency's subsequent risk findings and
consideration of possible risk mitigation measures. The proposed
interim registration review decision is supported by the rationale
included in those documents. Following public comment, the Agency will
issue an interim or final registration review decision for ethylene
oxide.
The registration review final rule at 40 CFR 155.58(a) provides for
a minimum 60-day public comment period on all proposed interim
registration review decisions. This comment period is intended to
provide an opportunity for public input and a mechanism for initiating
any necessary amendments to the proposed interim decision. All comments
should be submitted using the methods in ADDRESSES and must be received
by EPA on or before the closing date. These comments will become part
of the docket for ethylene oxide. Comments received after the close of
the comment period will be marked ``late.'' EPA is not required to
consider these late comments.
[[Page 22449]]
The Agency will carefully consider all comments received by the
closing date and may provide a ``Response to Comments Memorandum'' in
the docket. The interim registration review decision will explain the
effect that any comments had on the interim decision and provide the
Agency's response to significant comments.
Background on the registration review program is provided at:
https://www.epa.gov/pesticide-reevaluation.
Authority: 7 U.S.C. 136 et seq.
Dated: March 28, 2023.
Anita Pease,
Director, Antimicrobials Division, Office of Pesticide Programs.
[FR Doc. 2023-07727 Filed 4-12-23; 8:45 am]
BILLING CODE 6560-50-P