Methylene Chloride (MC); Draft Toxic Substances Control Act (TSCA) Risk Evaluation and TSCA Science Advisory Committee on Chemicals (SACC) Meeting; Notice of Availability, Public Meeting, and Request for Comment, 57866-57868 [2019-23614]
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Federal Register / Vol. 84, No. 209 / Tuesday, October 29, 2019 / Notices
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protesting or intervening; and (4)
otherwise comply with the requirements
of 18 CFR 385.2001 through 385.2005.
All comments, recommendations, terms
and conditions or prescriptions must set
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otherwise comply with the requirements
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copies of the application directly from
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Dated: October 23, 2019.
Kimberly D. Bose,
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[FR Doc. 2019–23588 Filed 10–28–19; 8:45 am]
BILLING CODE 6717–01–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2019–0437; FRL–9999–69]
Methylene Chloride (MC); Draft Toxic
Substances Control Act (TSCA) Risk
Evaluation and TSCA Science
Advisory Committee on Chemicals
(SACC) Meeting; Notice of Availability,
Public Meeting, and Request for
Comment
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
EPA is announcing the
availability of and soliciting public
comment on the draft Toxic Substances
Control Act (TSCA) risk evaluation of
Methylene Chloride (MC). The purpose
of the risk evaluation process under
TSCA is to determine, upon issuance of
a final risk evaluation, whether a
chemical substance presents an
unreasonable risk of injury to health or
the environment under the conditions of
use, including an unreasonable risk to a
relevant potentially exposed or
susceptible subpopulation. EPA is also
SUMMARY:
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submitting the same document to the
TSCA Science Advisory Committee on
Chemicals (SACC) for peer review and
is announcing that there will be an inperson public meeting of the TSCA
SACC to consider and review the draft
risk evaluation. Preceding the in-person
meeting, there will be a preparatory
virtual public meeting for the panel to
consider the scope and clarity of the
draft charge questions for the peer
review.
DATES:
Virtual Meeting: The preparatory
virtual meeting will be held on
November 12, 2019, from 1:00 p.m. to
approximately 4:00 p.m. (EST). You
must register online on or before
November 12, 2019 to receive the
webcast meeting link and audio
teleconference information. Submit your
written comments for the preparatory
virtual meeting, or request time to
present oral comments, on or before
noon, November 8, 2019.
In-Person Meeting: The in-person
meeting will be held on December 3–4,
2019, from 9:00 a.m. to approximately
5:30 p.m. (EST) each day. Any
comments submitted on the draft risk
evaluation on or before November 26,
2019 will be provided to the SACC to
allow them time to review and consider
them before the peer review meeting.
Comments received after November 26,
2019 and prior to the end of the oral
public comment period during the
meeting will be considered by EPA and
available to the SACC for their
consideration. Please submit requests to
present oral comments during the inperson meeting on or before December
3, 2019 to be included on the meeting
agenda.
Comments: All comments on the draft
risk evaluation must be received on or
before December 30, 2019.
For additional instructions, see Unit
III. of the SUPPLEMENTARY INFORMATION.
ADDRESSES: Virtual Meeting: Please visit
https://www.epa.gov/tsca-peer-review to
register.
In-Person Meeting: The in-person
meeting will be held at the Hyatt
Regency Crystal City, 2799 Jefferson
Davis Highway, Arlington, VA.
Additional meeting information can be
found on the TSCA SACC website at
https://www.epa.gov/tsca-peer-review.
Comments: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2019–0437 by
one of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Do not submit electronically any
information you consider to be
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Confidential Business Information (CBI)
or other information whose disclosure is
restricted by statute.
• Mail: OPPT Docket, Environmental
Protection Agency Docket Center (EPA/
DC), (28221T), 1200 Pennsylvania Ave.
NW, Washington, DC 20460–0001.
• Hand Delivery: To make special
arrangements for hand delivery or
delivery of boxed information, please
follow the instructions at https://
www.epa.gov/dockets/contacts.html.
Additional instructions on commenting
or visiting the docket, along with more
information about dockets generally, is
available at https://www.epa.gov/
dockets.
Requests to present oral comments
and requests for special
accommodations. Submit requests for
special accommodations, or requests to
present oral comments during the
virtual meeting and/or the in-person
peer review meeting, to the Designated
Federal Official (DFO) listed under FOR
FURTHER INFORMATION CONTACT by the
deadline identified in the DATES section.
FOR FURTHER INFORMATION CONTACT:
TSCA SACC meeting: Dr. Todd
Peterson, DFO, Office of Science
Coordination and Policy (7201M),
Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC
20460–0001; telephone number: (202)
564–6428; email address:
peterson.todd@epa.gov.
Draft Risk Evaluation: Dr. Stan
Barone, Office of Pollution Prevention
and Toxics (7403M), Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW, Washington, DC 20460–0001;
telephone number: (202) 564–1169;
email address: barone.stan@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
This action is directed to the public
in general. This action may be of
interest to persons who are or may be
required to conduct testing and those
interested in risk evaluations of
chemical substances under TSCA, 15
U.S.C. 2601 et seq. Since other entities
may also be interested in these draft risk
evaluations, the EPA has not attempted
to describe all the specific entities that
may be affected by this action.
B. What is EPA’s authority for taking
this action?
TSCA section 6, 15 U.S.C. 2605,
requires EPA to conduct risk
evaluations to ‘‘determine whether a
chemical substance presents an
unreasonable risk of injury to health or
the environment, without consideration
of costs or other nonrisk factors,
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including an unreasonable risk to a
potentially exposed or susceptible
subpopulation identified as relevant to
the risk evaluation by the
Administrator, under the conditions of
use.’’ 15 U.S.C. 2605(b)(4)(A). TSCA
sections 6(b)(4)(A) through (H)
enumerate the deadlines and minimum
requirements applicable to this process,
including provisions that provide
instruction on chemical substances that
must undergo evaluation, the minimum
components of a TSCA risk evaluation,
and the timelines for public comment
and completion of the risk evaluation.
TSCA also requires that EPA operate in
a manner that is consistent with the best
available science, make decisions based
on the weight of the scientific evidence
and consider reasonably available
information. 15 U.S.C. 2625(h), (i), and
(k).
The statute identifies the minimum
components for all chemical substance
risk evaluations. For each risk
evaluation, EPA must publish a
document that outlines the scope of the
risk evaluation to be conducted, which
includes the hazards, exposures,
conditions of use, and the potentially
exposed or susceptible subpopulations
that EPA expects to consider. 15 U.S.C.
2605(b)(4)(D). The statute further
provides that each risk evaluation must
also: (1) Integrate and assess available
information on hazards and exposures
for the conditions of use of the chemical
substance, including information on
specific risks of injury to health or the
environment and information on
relevant potentially exposed or
susceptible subpopulations; (2) describe
whether aggregate or sentinel exposures
were considered and the basis for that
consideration; (3) take into account,
where relevant, the likely duration,
intensity, frequency, and number of
exposures under the conditions of use;
and (4) describe the weight of the
scientific evidence for the identified
hazards and exposures. 15 U.S.C.
2605(b)(4)(F)(i)–(ii) and (iv)–(v). Each
risk evaluation must not consider costs
or other nonrisk factors. 15 U.S.C.
2605(b)(4)(F)(iii).
The statute requires that the risk
evaluation process last no longer than
three years, with a possible additional
six-month extension. 15 U.S.C.
2605(b)(4)(G). The statute also requires
that the EPA allow for no less than a 30day public comment period on the draft
risk evaluation, prior to publishing a
final risk evaluation. 15 U.S.C.
2605(b)(4)(H).
C. What action is EPA taking?
EPA is announcing the availability of
and seeking public comment on the
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draft risk evaluation of the chemical
substances identified in Unit II. EPA is
seeking public comment on all aspects
of the draft risk evaluation, including
any preliminary conclusions, findings,
and determinations, and the submission
of any additional information that might
be relevant to the draft risk evaluation,
including the science underlying the
draft risk evaluation and the outcome of
the systematic review associated with
the chemical substances. This 60-day
comment period on the draft risk
evaluation satisfies TSCA section
6(b)(4)(H), which requires EPA to
‘‘provide no less than 30 days public
notice and an opportunity for comment
on a draft risk evaluation prior to
publishing a final risk evaluation,’’ and
40 CFR 702.49(a), which states that
‘‘EPA will publish a draft risk
evaluation in the Federal Register, open
a docket to facilitate receipt of public
comment, and provide no less than a 60day comment period, during which time
the public may submit comment on
EPA’s draft risk evaluation.’’ In addition
to any new comments on the draft risk
evaluation, the public should resubmit
or clearly identify any previously filed
comments, modified as appropriate, that
are relevant to the draft risk evaluation
and that the submitter feels have not
been addressed. EPA does not intend to
respond to comments submitted prior to
the release of the draft risk evaluation
unless they are clearly identified in
comments on the draft risk evaluation.
EPA is also submitting the draft risk
evaluation and associated supporting
documents to the TSCA SACC for peer
review and announcing the meeting for
the peer review panel. All comments
submitted to the dockets on the draft
risk evaluation by the deadline
identified in the DATES section will be
provided for consideration to the TSCA
SACC peer review panel, which will
have the opportunity to consider the
comments during its discussions.
D. 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 in 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 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
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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/
comments.html.
II. Draft TSCA Risk Evaluation
A. What is EPA’s risk evaluation process
for existing chemicals under TSCA?
The risk evaluation process is the
second step in EPA’s existing chemical
process under TSCA, following
prioritization and before risk
management. As these chemicals are
part of the first ten chemical substances
undergoing risk evaluation, these
chemical substances were not required
to go through prioritization (81 FR
91927, December 19, 2016) (FRL–9956–
47). The purpose of risk evaluation is to
determine whether a chemical
substance presents an unreasonable risk
of injury to health or the environment,
under the conditions of use, including
an unreasonable risk to a relevant
potentially exposed or susceptible
subpopulation. As part of this process,
EPA must evaluate both hazard and
exposure, not consider costs or other
nonrisk factors, use reasonably available
information and approaches in a
manner that is consistent with the
requirements in TSCA for the use of the
best available science, and ensure
decisions are based on the weight-ofscientific-evidence.
The specific risk evaluation process
that EPA has established by rule to
implement the statutory process is set
out in 40 CFR part 702 and summarized
on EPA’s website at https://
www.epa.gov/assessing-and-managingchemicals-under-tsca/risk-evaluationsexisting-chemicals-under-tsca. As
explained in the preamble to EPA’s final
rule on procedures for risk evaluation
(82 FR 33726, July 20, 2017) (FRL–
9964–38), the specific regulatory
process set out in 40 CFR part 702,
subpart B will be followed for the first
ten chemical substances undergoing risk
evaluation to the maximum extent
practicable.
B. What is MC?
Methylene chloride (MC), also known
as dichloromethane and DCM, is a
volatile chemical used as a solvent in a
wide range of industrial, commercial
and consumer applications. The
primary uses for methylene chloride are
for paint removal, adhesives,
pharmaceutical manufacturing, metal
cleaning, aerosol solvents, chemical
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processing and flexible polyurethane
foam manufacturing. Information from
the 2016 Chemical Data Reporting (CDR)
for MC indicates the reported
production volume is more than 260
million lbs/year (manufacture and
import).
Information about the problem
formulation and scope phases of the
TSCA risk evaluation for this chemical
is available at https://www.epa.gov/
assessing-and-managing-chemicalsunder-tsca/risk-evaluation-methylenechloride-0.
III. TSCA SACC
A. What is the purpose of the TSCA
SACC?
The TSCA SACC was established by
EPA in 2016 and operates in accordance
with the Federal Advisory Committee
Act (FACA), 5 U.S.C. Appendix 2 et seq.
The TSCA SACC provides expert
independent scientific advice and
consultation to the EPA on the scientific
and technical aspects of risk
assessments, methodologies, and
pollution prevention measures and
approaches for chemicals regulated
under TSCA.
The TSCA SACC is comprised of
experts in: Toxicology; human health
and environmental risk assessment;
exposure assessment; and related
sciences (e.g., synthetic biology,
pharmacology, biotechnology,
nanotechnology, biochemistry,
biostatistics, physiologically based
pharmacokinetic modelling (PBPK)
modeling, computational toxicology,
epidemiology, environmental fate, and
environmental engineering and
sustainability). When needed, the
committee will be assisted in their
reviews by ad hoc participants with
specific expertise in the topics under
consideration.
B. How can I access the TSCA SACC
documents?
EPA’s background documents, related
supporting materials, and draft charge
questions to the TSCA SACC are
available on the TSCA SACC website
and in the docket established for the
specific chemical substances. In
addition, EPA will provide additional
background documents (e.g., TSCA
SACC members participating in this
meeting and the meeting agenda) as the
materials become available. You may
obtain electronic copies of these
documents, and certain other related
documents that might be available, in
the docket at https://www.regulations.gov
and the TSCA SACC website at https://
www.epa.gov/tsca-peer-review.
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After the public meeting, the TSCA
SACC will prepare meeting minutes
summarizing its recommendations to
EPA. The meeting minutes will be
posted on the TSCA SACC website and
in the relevant docket.
C. What do I need to know about the
TSCA SACC public meetings?
The focus of the public meeting is to
peer review EPA’s draft risk evaluation.
After the peer review process, EPA will
consider peer reviewer comments and
recommendations, and public
comments, in finalizing the risk
evaluation. The draft risk evaluation
contains: Discussion of chemistry and
physical-chemical properties;
characterization of conditions of use;
environmental fate and transport
assessment; human health exposures;
environmental hazard assessment; risk
characterization; risk determination;
and a detailed description of the
systematic review process developed by
the Office of Pollution Prevention and
Toxics to search, screen, and evaluate
scientific literature for use in the risk
evaluation process.
D. How do I participate in the public
meetings?
You may participate in the public
meetings by following the instructions
in this unit. To ensure proper receipt by
EPA, it is imperative that you identify
the corresponding docket ID number in
the subject line on the first page of your
request.
1. Preparatory virtual meeting. The
preparatory virtual meeting will be
conducted via webcast and telephone.
You may participate in the preparatory
virtual meeting by registering to join the
webcast. You may also submit written
comments or request time for oral
comments.
i. Registration. You must register to
participate in the preparatory virtual
meeting. To participate by listening or
making a comment during this meeting,
please go to the EPA website to register:
https://www.epa.gov/tsca-peer-review.
Registration online will be confirmed by
an email that will include the webcast
meeting link and audio teleconference
information.
ii. Written comments. Written
comments for consideration during the
preparatory virtual meeting should be
submitted, using the instructions in
ADDRESSES and this unit, on or before
the date set in the DATES section.
iii. Oral comments. Requests to make
brief oral comments to the TSCA SACC
during the preparatory virtual meeting
should be submitted when registering
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online or with the DFO listed under FOR
FURTHER INFORMATION CONTACT on or
before noon on the date set in the DATES
section. Oral comments before the TSCA
SACC during the preparatory virtual
meeting are limited to approximately 5
minutes due to the time constraints of
this virtual meeting.
2. In-person meeting. You may
participate in the in-person public
meeting by attending and by providing
written or oral comments. The in-person
meeting may also be webcast. Please
refer to the TSCA SACC website at
https://www.epa.gov/tsca-peer-review for
information on how to access the
webcast. Please note that for the inperson meeting, the webcast is a
supplementary public process provided
only for convenience. If difficulties arise
resulting in webcasting outages, the inperson meeting will continue as
planned.
i. Seating at the meeting. Seating at
the meeting will be open and on a firstcome basis.
ii. Written comments. To provide the
TSCA SACC the time necessary to
consider and review your comments,
written comments must be submitted by
the date set in the DATES section and
using the instructions in the ADDRESSES
section and this unit. Comments
received after the date set in the DATES
section and prior to the end of the oral
public comment period during the
meeting will still be provided to the
TSCA SACC for their consideration.
iii. Oral comments. To be included on
the meeting agenda, submit your request
to make brief oral comments at the inperson meeting to the DFO listed under
FOR FURTHER INFORMATION CONTACT on or
before the date set in the DATES section.
The request should identify the name of
the individual making the presentation,
the organization (if any) the individual
will represent, and any requirements for
audiovisual equipment. Oral comments
before TSCA SACC during the in-person
meeting are limited to approximately 5
minutes unless prior arrangements have
been made. In addition, each speaker
should bring 30 copies of the comments
and presentation for distribution by the
DFO to the TSCA SACC at the meeting.
Authority: 15 U.S.C. 2601 et seq.
Dated: October 23, 2019.
Andrew R. Wheeler,
Administrator.
[FR Doc. 2019–23614 Filed 10–24–19; 4:15 pm]
BILLING CODE 6560–50–P
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Agencies
[Federal Register Volume 84, Number 209 (Tuesday, October 29, 2019)]
[Notices]
[Pages 57866-57868]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-23614]
=======================================================================
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ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPPT-2019-0437; FRL-9999-69]
Methylene Chloride (MC); Draft Toxic Substances Control Act
(TSCA) Risk Evaluation and TSCA Science Advisory Committee on Chemicals
(SACC) Meeting; Notice of Availability, Public Meeting, and Request for
Comment
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: EPA is announcing the availability of and soliciting public
comment on the draft Toxic Substances Control Act (TSCA) risk
evaluation of Methylene Chloride (MC). The purpose of the risk
evaluation process under TSCA is to determine, upon issuance of a final
risk evaluation, whether a chemical substance presents an unreasonable
risk of injury to health or the environment under the conditions of
use, including an unreasonable risk to a relevant potentially exposed
or susceptible subpopulation. EPA is also submitting the same document
to the TSCA Science Advisory Committee on Chemicals (SACC) for peer
review and is announcing that there will be an in-person public meeting
of the TSCA SACC to consider and review the draft risk evaluation.
Preceding the in-person meeting, there will be a preparatory virtual
public meeting for the panel to consider the scope and clarity of the
draft charge questions for the peer review.
DATES:
Virtual Meeting: The preparatory virtual meeting will be held on
November 12, 2019, from 1:00 p.m. to approximately 4:00 p.m. (EST). You
must register online on or before November 12, 2019 to receive the
webcast meeting link and audio teleconference information. Submit your
written comments for the preparatory virtual meeting, or request time
to present oral comments, on or before noon, November 8, 2019.
In-Person Meeting: The in-person meeting will be held on December
3-4, 2019, from 9:00 a.m. to approximately 5:30 p.m. (EST) each day.
Any comments submitted on the draft risk evaluation on or before
November 26, 2019 will be provided to the SACC to allow them time to
review and consider them before the peer review meeting. Comments
received after November 26, 2019 and prior to the end of the oral
public comment period during the meeting will be considered by EPA and
available to the SACC for their consideration. Please submit requests
to present oral comments during the in-person meeting on or before
December 3, 2019 to be included on the meeting agenda.
Comments: All comments on the draft risk evaluation must be
received on or before December 30, 2019.
For additional instructions, see Unit III. of the SUPPLEMENTARY
INFORMATION.
ADDRESSES: Virtual Meeting: Please visit https://www.epa.gov/tsca-peer-review to register.
In-Person Meeting: The in-person meeting will be held at the Hyatt
Regency Crystal City, 2799 Jefferson Davis Highway, Arlington, VA.
Additional meeting information can be found on the TSCA SACC website at
https://www.epa.gov/tsca-peer-review.
Comments: Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPPT-2019-0437 by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow 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.
Mail: OPPT Docket, Environmental Protection Agency Docket
Center (EPA/DC), (28221T), 1200 Pennsylvania Ave. NW, Washington, DC
20460-0001.
Hand Delivery: To make special arrangements for hand
delivery or delivery of boxed information, please follow the
instructions at https://www.epa.gov/dockets/contacts.html. Additional
instructions on commenting or visiting the docket, along with more
information about dockets generally, is available at https://www.epa.gov/dockets.
Requests to present oral comments and requests for special
accommodations. Submit requests for special accommodations, or requests
to present oral comments during the virtual meeting and/or the in-
person peer review meeting, to the Designated Federal Official (DFO)
listed under FOR FURTHER INFORMATION CONTACT by the deadline identified
in the DATES section.
FOR FURTHER INFORMATION CONTACT: TSCA SACC meeting: Dr. Todd Peterson,
DFO, Office of Science Coordination and Policy (7201M), Environmental
Protection Agency, 1200 Pennsylvania Ave. NW, Washington, DC 20460-
0001; telephone number: (202) 564-6428; email address:
[email protected].
Draft Risk Evaluation: Dr. Stan Barone, Office of Pollution
Prevention and Toxics (7403M), Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC 20460-0001; telephone number:
(202) 564-1169; email address: [email protected].
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
This action is directed to the public in general. This action may
be of interest to persons who are or may be required to conduct testing
and those interested in risk evaluations of chemical substances under
TSCA, 15 U.S.C. 2601 et seq. Since other entities may also be
interested in these draft risk evaluations, the EPA has not attempted
to describe all the specific entities that may be affected by this
action.
B. What is EPA's authority for taking this action?
TSCA section 6, 15 U.S.C. 2605, requires EPA to conduct risk
evaluations to ``determine whether a chemical substance presents an
unreasonable risk of injury to health or the environment, without
consideration of costs or other nonrisk factors,
[[Page 57867]]
including an unreasonable risk to a potentially exposed or susceptible
subpopulation identified as relevant to the risk evaluation by the
Administrator, under the conditions of use.'' 15 U.S.C. 2605(b)(4)(A).
TSCA sections 6(b)(4)(A) through (H) enumerate the deadlines and
minimum requirements applicable to this process, including provisions
that provide instruction on chemical substances that must undergo
evaluation, the minimum components of a TSCA risk evaluation, and the
timelines for public comment and completion of the risk evaluation.
TSCA also requires that EPA operate in a manner that is consistent with
the best available science, make decisions based on the weight of the
scientific evidence and consider reasonably available information. 15
U.S.C. 2625(h), (i), and (k).
The statute identifies the minimum components for all chemical
substance risk evaluations. For each risk evaluation, EPA must publish
a document that outlines the scope of the risk evaluation to be
conducted, which includes the hazards, exposures, conditions of use,
and the potentially exposed or susceptible subpopulations that EPA
expects to consider. 15 U.S.C. 2605(b)(4)(D). The statute further
provides that each risk evaluation must also: (1) Integrate and assess
available information on hazards and exposures for the conditions of
use of the chemical substance, including information on specific risks
of injury to health or the environment and information on relevant
potentially exposed or susceptible subpopulations; (2) describe whether
aggregate or sentinel exposures were considered and the basis for that
consideration; (3) take into account, where relevant, the likely
duration, intensity, frequency, and number of exposures under the
conditions of use; and (4) describe the weight of the scientific
evidence for the identified hazards and exposures. 15 U.S.C.
2605(b)(4)(F)(i)-(ii) and (iv)-(v). Each risk evaluation must not
consider costs or other nonrisk factors. 15 U.S.C. 2605(b)(4)(F)(iii).
The statute requires that the risk evaluation process last no
longer than three years, with a possible additional six-month
extension. 15 U.S.C. 2605(b)(4)(G). The statute also requires that the
EPA allow for no less than a 30-day public comment period on the draft
risk evaluation, prior to publishing a final risk evaluation. 15 U.S.C.
2605(b)(4)(H).
C. What action is EPA taking?
EPA is announcing the availability of and seeking public comment on
the draft risk evaluation of the chemical substances identified in Unit
II. EPA is seeking public comment on all aspects of the draft risk
evaluation, including any preliminary conclusions, findings, and
determinations, and the submission of any additional information that
might be relevant to the draft risk evaluation, including the science
underlying the draft risk evaluation and the outcome of the systematic
review associated with the chemical substances. This 60-day comment
period on the draft risk evaluation satisfies TSCA section 6(b)(4)(H),
which requires EPA to ``provide no less than 30 days public notice and
an opportunity for comment on a draft risk evaluation prior to
publishing a final risk evaluation,'' and 40 CFR 702.49(a), which
states that ``EPA will publish a draft risk evaluation in the Federal
Register, open a docket to facilitate receipt of public comment, and
provide no less than a 60-day comment period, during which time the
public may submit comment on EPA's draft risk evaluation.'' In addition
to any new comments on the draft risk evaluation, the public should
resubmit or clearly identify any previously filed comments, modified as
appropriate, that are relevant to the draft risk evaluation and that
the submitter feels have not been addressed. EPA does not intend to
respond to comments submitted prior to the release of the draft risk
evaluation unless they are clearly identified in comments on the draft
risk evaluation.
EPA is also submitting the draft risk evaluation and associated
supporting documents to the TSCA SACC for peer review and announcing
the meeting for the peer review panel. All comments submitted to the
dockets on the draft risk evaluation by the deadline identified in the
DATES section will be provided for consideration to the TSCA SACC peer
review panel, which will have the opportunity to consider the comments
during its discussions.
D. 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 in 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 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/comments.html.
II. Draft TSCA Risk Evaluation
A. What is EPA's risk evaluation process for existing chemicals under
TSCA?
The risk evaluation process is the second step in EPA's existing
chemical process under TSCA, following prioritization and before risk
management. As these chemicals are part of the first ten chemical
substances undergoing risk evaluation, these chemical substances were
not required to go through prioritization (81 FR 91927, December 19,
2016) (FRL-9956-47). The purpose of risk evaluation is to determine
whether a chemical substance presents an unreasonable risk of injury to
health or the environment, under the conditions of use, including an
unreasonable risk to a relevant potentially exposed or susceptible
subpopulation. As part of this process, EPA must evaluate both hazard
and exposure, not consider costs or other nonrisk factors, use
reasonably available information and approaches in a manner that is
consistent with the requirements in TSCA for the use of the best
available science, and ensure decisions are based on the weight-of-
scientific-evidence.
The specific risk evaluation process that EPA has established by
rule to implement the statutory process is set out in 40 CFR part 702
and summarized on EPA's website at https://www.epa.gov/assessing-and-managing-chemicals-under-tsca/risk-evaluations-existing-chemicals-under-tsca. As explained in the preamble to EPA's final rule on
procedures for risk evaluation (82 FR 33726, July 20, 2017) (FRL-9964-
38), the specific regulatory process set out in 40 CFR part 702,
subpart B will be followed for the first ten chemical substances
undergoing risk evaluation to the maximum extent practicable.
B. What is MC?
Methylene chloride (MC), also known as dichloromethane and DCM, is
a volatile chemical used as a solvent in a wide range of industrial,
commercial and consumer applications. The primary uses for methylene
chloride are for paint removal, adhesives, pharmaceutical
manufacturing, metal cleaning, aerosol solvents, chemical
[[Page 57868]]
processing and flexible polyurethane foam manufacturing. Information
from the 2016 Chemical Data Reporting (CDR) for MC indicates the
reported production volume is more than 260 million lbs/year
(manufacture and import).
Information about the problem formulation and scope phases of the
TSCA risk evaluation for this chemical is available at https://www.epa.gov/assessing-and-managing-chemicals-under-tsca/risk-evaluation-methylene-chloride-0.
III. TSCA SACC
A. What is the purpose of the TSCA SACC?
The TSCA SACC was established by EPA in 2016 and operates in
accordance with the Federal Advisory Committee Act (FACA), 5 U.S.C.
Appendix 2 et seq. The TSCA SACC provides expert independent scientific
advice and consultation to the EPA on the scientific and technical
aspects of risk assessments, methodologies, and pollution prevention
measures and approaches for chemicals regulated under TSCA.
The TSCA SACC is comprised of experts in: Toxicology; human health
and environmental risk assessment; exposure assessment; and related
sciences (e.g., synthetic biology, pharmacology, biotechnology,
nanotechnology, biochemistry, biostatistics, physiologically based
pharmacokinetic modelling (PBPK) modeling, computational toxicology,
epidemiology, environmental fate, and environmental engineering and
sustainability). When needed, the committee will be assisted in their
reviews by ad hoc participants with specific expertise in the topics
under consideration.
B. How can I access the TSCA SACC documents?
EPA's background documents, related supporting materials, and draft
charge questions to the TSCA SACC are available on the TSCA SACC
website and in the docket established for the specific chemical
substances. In addition, EPA will provide additional background
documents (e.g., TSCA SACC members participating in this meeting and
the meeting agenda) as the materials become available. You may obtain
electronic copies of these documents, and certain other related
documents that might be available, in the docket at https://www.regulations.gov and the TSCA SACC website at https://www.epa.gov/tsca-peer-review.
After the public meeting, the TSCA SACC will prepare meeting
minutes summarizing its recommendations to EPA. The meeting minutes
will be posted on the TSCA SACC website and in the relevant docket.
C. What do I need to know about the TSCA SACC public meetings?
The focus of the public meeting is to peer review EPA's draft risk
evaluation. After the peer review process, EPA will consider peer
reviewer comments and recommendations, and public comments, in
finalizing the risk evaluation. The draft risk evaluation contains:
Discussion of chemistry and physical-chemical properties;
characterization of conditions of use; environmental fate and transport
assessment; human health exposures; environmental hazard assessment;
risk characterization; risk determination; and a detailed description
of the systematic review process developed by the Office of Pollution
Prevention and Toxics to search, screen, and evaluate scientific
literature for use in the risk evaluation process.
D. How do I participate in the public meetings?
You may participate in the public meetings by following the
instructions in this unit. To ensure proper receipt by EPA, it is
imperative that you identify the corresponding docket ID number in the
subject line on the first page of your request.
1. Preparatory virtual meeting. The preparatory virtual meeting
will be conducted via webcast and telephone. You may participate in the
preparatory virtual meeting by registering to join the webcast. You may
also submit written comments or request time for oral comments.
i. Registration. You must register to participate in the
preparatory virtual meeting. To participate by listening or making a
comment during this meeting, please go to the EPA website to register:
https://www.epa.gov/tsca-peer-review. Registration online will be
confirmed by an email that will include the webcast meeting link and
audio teleconference information.
ii. Written comments. Written comments for consideration during the
preparatory virtual meeting should be submitted, using the instructions
in ADDRESSES and this unit, on or before the date set in the DATES
section.
iii. Oral comments. Requests to make brief oral comments to the
TSCA SACC during the preparatory virtual meeting should be submitted
when registering online or with the DFO listed under FOR FURTHER
INFORMATION CONTACT on or before noon on the date set in the DATES
section. Oral comments before the TSCA SACC during the preparatory
virtual meeting are limited to approximately 5 minutes due to the time
constraints of this virtual meeting.
2. In-person meeting. You may participate in the in-person public
meeting by attending and by providing written or oral comments. The in-
person meeting may also be webcast. Please refer to the TSCA SACC
website at https://www.epa.gov/tsca-peer-review for information on how
to access the webcast. Please note that for the in-person meeting, the
webcast is a supplementary public process provided only for
convenience. If difficulties arise resulting in webcasting outages, the
in-person meeting will continue as planned.
i. Seating at the meeting. Seating at the meeting will be open and
on a first-come basis.
ii. Written comments. To provide the TSCA SACC the time necessary
to consider and review your comments, written comments must be
submitted by the date set in the DATES section and using the
instructions in the ADDRESSES section and this unit. Comments received
after the date set in the DATES section and prior to the end of the
oral public comment period during the meeting will still be provided to
the TSCA SACC for their consideration.
iii. Oral comments. To be included on the meeting agenda, submit
your request to make brief oral comments at the in-person meeting to
the DFO listed under FOR FURTHER INFORMATION CONTACT on or before the
date set in the DATES section. The request should identify the name of
the individual making the presentation, the organization (if any) the
individual will represent, and any requirements for audiovisual
equipment. Oral comments before TSCA SACC during the in-person meeting
are limited to approximately 5 minutes unless prior arrangements have
been made. In addition, each speaker should bring 30 copies of the
comments and presentation for distribution by the DFO to the TSCA SACC
at the meeting.
Authority: 15 U.S.C. 2601 et seq.
Dated: October 23, 2019.
Andrew R. Wheeler,
Administrator.
[FR Doc. 2019-23614 Filed 10-24-19; 4:15 pm]
BILLING CODE 6560-50-P