Procedures for Prioritization of Chemicals for Risk Evaluation Under the Toxic Substances Control Act, 33753-33764 [2017-14325]
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and provide no less than a 60-day
comment period, during which time the
public may submit comment on EPA’s
draft risk evaluation.
(b) Final risk evaluation. (1) EPA will
complete a risk evaluation for the
chemical substance under the
conditions of use within the scope of
the risk evaluation as soon as
practicable, but not later than 3 years
after the date on which the Agency
initiates the risk evaluation.
(2) The Agency may extend the
deadline for a risk evaluation for not
more than 6 months. The total time
elapsed between initiation of the risk
evaluation and completion of the risk
evaluation may not exceed 3 and one
half years.
(3) EPA will publish the final risk
evaluation in the Federal Register.
(c) Final determination of
unreasonable risk. Upon determination
by the EPA that a chemical substance
under one or more of the conditions of
use within the scope of the risk
evaluation presents an unreasonable
risk of injury to health or the
environment as described in § 702.47,
the Agency will initiate action as
required pursuant to 15 U.S.C. 2605(a).
(d) Final determination of no
unreasonable risk. A determination by
EPA that the chemical substance, under
one or more of the conditions of use
within the scope of the risk evaluation,
does not present an unreasonable risk of
injury to health or the environment will
be issued by order and considered to be
a final Agency action, effective on the
date of issuance of the order.
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§ 702.51
Publically available information.
For each risk evaluation, EPA will
maintain a public docket at https://
www.regulations.gov to provide public
access to the following information, as
applicable for that risk evaluation:
(a) The draft scope, final scope, draft
risk evaluation, and final risk
evaluation;
(b) All notices, determinations,
findings, consent agreements, and
orders;
(c) Any information required to be
provided to the Agency under 15 U.S.C.
2603;
(d) A nontechnical summary of the
risk evaluation;
(e) A list of the studies, with the
results of the studies, considered in
carrying out each risk evaluation;
(f) The final peer review report,
including the response to peer review
and public comments received during
peer review; and
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(g) Response to public comments
received on the draft scope and the draft
risk evaluation.
[FR Doc. 2017–14337 Filed 7–19–17; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 702
33753
Toxics, Environmental Protection
Agency, 1200 Pennsylvania Ave. NW.,
Washington, DC 20460–0001; telephone
number: (202) 564–4321; email address:
blair.susanna@epa.gov.
For general information contact: The
TSCA-Hotline, ABVI-Goodwill, 422
South Clinton Ave., Rochester, NY
14620; telephone number: (202) 554–
1404; email address: TSCA-Hotline@
epa.gov.
[EPA–HQ–OPPT–2016–0636; FRL–9964–24]
SUPPLEMENTARY INFORMATION:
RIN 2070–AK23
I. Executive Summary
Procedures for Prioritization of
Chemicals for Risk Evaluation Under
the Toxic Substances Control Act
A. What action is the Agency taking?
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
As required under section
6(b)(1) of the Toxic Substances Control
Act (TSCA), EPA is issuing a final rule
that establishes the process and criteria
that EPA will use to identify chemical
substances as either High-Priority
Substances for risk evaluation, or LowPriority Substances for which risk
evaluations are not warranted at the
time. The final rule describes the
processes for formally initiating the
prioritization process on a selected
candidate, providing opportunities for
public comment, screening the
candidate against certain criteria, and
proposing and finalizing designations of
priority. Prioritization is the initial step
in a new process of existing chemical
substance review and risk management
activity established under TSCA.
DATES: This final rule is effective
September 18, 2017.
ADDRESSES: The docket for this action,
identified by docket identification (ID)
number EPA–HQ–OPPT–2016–0636, is
available at https://www.regulations.gov
or at the Office of Pollution Prevention
and Toxics Docket (OPPT Docket) in the
Environmental Protection Agency
Docket Center (EPA/DC), West William
Jefferson Clinton Bldg., Rm. 3334, 1301
Constitution Ave. NW., Washington, DC
20460–0001. The Public Reading Room
is open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room is (202) 566–1744,
and the telephone number for the OPPT
Docket is (202) 566–0280. Please review
the visitor instructions and additional
information about the docket available
at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
For technical information contact:
Susanna W. Blair, Immediate Office,
Office of Pollution Prevention and
SUMMARY:
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EPA is promulgating this final rule to
establish the process and criteria by
which EPA will identify chemical
substances as either High-Priority
Substances for risk evaluation, or LowPriority Substances for which risk
evaluations are not warranted at the
time.
B. Does this action apply to me?
This final rule does not establish any
requirements on persons or entities
outside of the Agency. This action may,
however, be of interest to entities that
are manufacturing or may manufacture
or import a chemical substance
regulated under TSCA (e.g., entities
identified under North American
Industrial Classification System
(NAICS) codes 325 and 324110). Since
other entities may also be interested, the
Agency has not attempted to describe all
the specific entities and corresponding
NAICS codes for entities that may be
interested in or affected by this action.
C. Why is the Agency taking this action?
This rulemaking is required by TSCA
section 6(b)(1)(A), 15 U.S.C.
2605(b)(1)(A). Prioritization of chemical
substances for further evaluation will
help to ensure that the Agency’s limited
resources are conserved for those
chemical substances most likely to
present risks, thereby furthering EPA’s
overall mission to protect health and the
environment.
D. What is the Agency’s authority for
taking this action?
This final rule is issued pursuant to
the authority in TSCA section 6(b), 15
U.S.C. 2605(b).
E. What are the estimated incremental
impacts of this action?
This final rule establishes the
processes by which EPA intends to
designate chemical substances as either
High or Low-Priority Substances for risk
evaluation. It does not establish any
requirements on persons or entities
outside of the Agency. No incremental
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impacts are therefore anticipated, and
consequently EPA did not estimate
potential incremental impacts from this
action.
II. Background
A. Statutory Requirements for
Prioritization
TSCA section 6(b)(1), as amended by
the Frank R. Lautenberg Chemical
Safety for the 21st Century Act (Pub. L.
114–182), requires EPA to establish, by
rule, a process for prioritizing chemical
substances for risk evaluation.
Specifically, the law requires EPA to
establish ‘‘a risk-based screening
process, including criteria for
designating chemical substances as
high-priority substances for risk
evaluations or low-priority substances
for which risk evaluations are not
warranted at the time.’’ 15 U.S.C.
2605(b)(1)(A). TSCA sections 6(b)(1)
through (3) provide further specificity
on both the process and criteria,
including preferences for certain
chemical substances that EPA must
apply, procedural steps, definitions of
High-Priority Substances and LowPriority Substances, and screening
criteria that EPA must consider in
designating a chemical substance as
either a High-Priority Substance or a
Low-Priority Substance. 15 U.S.C.
2605(b)(1)–(3).
EPA published a proposed rule on
January 17, 2017 setting forth the draft
process and criteria (Ref. 1). A detailed
summary of the statutory requirements
for prioritization, EPA’s methodology
for prioritizing existing chemicals for
assessment under the TSCA Work Plan
before enactment of the TSCA
amendments in 2016, and pre-proposal
stakeholder involvement activities and
feedback was presented in the proposed
rule.
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B. Interagency Collaboration
EPA is committed to engaging and
collaborating with partner federal
agencies prior to and during the
prioritization process. TSCA specifically
authorizes other federal agencies, at
EPA’s request, to: (1) Make their
services, personnel, and facilities
available to the Agency, (2) provide
information, data, estimates, and
statistics to the Agency, and (3) grant
EPA access to all information in its
possession as the Agency may
reasonably determine to be necessary for
the administration of the Act. 15 U.S.C.
2625(a). EPA has a number of existing
mechanisms already in place to
facilitate collaboration with the
Agency’s federal partners and will
continue to utilize them. Collaboration
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with other federal agencies is an
important step in identifying chemicals
for prioritization, evaluating risks from
chemicals, and during the risk
management phase, if a chemical use is
determined to present an unreasonable
risk.
EPA’s collaboration with other federal
agencies prior to and during the riskbased prioritization process gives other
agencies sufficient time to work with
the EPA in identifying any information
about a particular chemical substance
that may be useful for formulating a
priority designation for that substance
(e.g., conditions of use, exposure
scenarios, etc.). The Agency anticipates
that it will at times collaborate with the
other statutory member agencies of the
TSCA Interagency Testing Committee
(ITC), i.e., the Consumer Product Safety
Commission (CPSC), the Council on
Environmental Quality (CEQ),
Department of Commerce, the Food and
Drug Administration (FDA), the
National Cancer Institute (NCI), the
National Institute of Environmental
Health Sciences (NIEHS), the National
Institute for Occupational Safety and
Health (NIOSH), the National Science
Foundation (NSF); and the
Occupational Safety and Health
Administration (OSHA). 15 U.S.C.
2603(e)(2)(A). EPA also expects that
such collaboration will extend, when
appropriate, to other federal agency
partners not specifically identified in
TSCA as ITC members, such as the
Agency for Toxic Substances Disease
Registry (ATSDR), the Department of
Defense, the National Aeronautics and
Space Administration (NASA), and the
Office of Management and Budget
(OMB). Finally, EPA anticipates that its
collaboration with other federal
agencies may include, when
appropriate, the Small Business
Administration’s Office of Advocacy
and various other agencies to help
facilitate outreach to the business sector.
III. Overview of the Final Rule
This final rule incorporates all of the
elements required by statute, some
additional criteria the Agency expects to
consider, clarifications for greater
transparency, and additional procedural
steps to ensure effective
implementation. In response to public
comments on the proposal, EPA is,
among other things: (1) Deleting the preprioritization provisions, and
committing to further public comment
on how the Agency will identify
candidates for prioritization, (2) adding
direct references in the final regulation
to acknowledge the Agency’s
commitment to implementing the best
available science and weight of the
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scientific evidence provisions in TSCA,
and (3) adding a number of provisions
to clarify the limited meaning of a
priority designation, and committing the
Agency to clear and effective
communication throughout the process.
EPA intends that the provisions of
this rule be severable. In the event that
any individual provision or part of this
rule is invalidated, EPA intends that
this would not render the entire rule
invalid, and that any individual
provisions that can continue to operate
will be left in place.
IV. Detailed Discussion of Final Rule
and Response to Comments
This unit provides a more in-depth
discussion of the provisions in the final
rule, public comments received on the
proposal, and revisions made to the rule
in response. A separate document that
summarizes all comments submitted on
the proposal and EPA’s responses to
those comments has been prepared and
is available in the docket for this
rulemaking (Ref. 2).
A. Policy Objective
The final rule adopts the proposed
codification of the policy objective
without revision. The prioritization
process serves a limited, but important,
purpose in the new pipeline of existing
chemical review and management to
help the Agency identify priorities for
further risk evaluation, to ensure that
those priorities are grounded in riskbased considerations (which may
include, among other considerations,
the nature and extent of any existing
regulation that is intended to mitigate
the hazards of a chemical substance),
and to provide the public and interested
stakeholders with notice and an
opportunity to engage with the Agency
and provide relevant information prior
to the start of the risk evaluation process
on a particular chemical. Through the
process of prioritization, EPA is
ultimately making a judgment as to
whether or not a particular chemical
substance warrants further assessment.
As a general matter, the primary
objective of the process should be to
guide the Agency towards identifying
the High-Priority Substances that have
the greatest hazard and exposure
potential first. The prioritization process
is not intended to be an exact scoring or
ranking exercise and, consistent with
the proposed rule, EPA is not adopting
such a system in this rule. The precise
order (e.g., ranking or ordering
chemicals based on their hazard and
exposure potential) in which EPA
identifies High-Priority Substances (all
of which must meet the same statutory
definition) should not be allowed to
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slow the Agency’s progress towards
evaluating the risks from those chemical
substances. EPA intends to conserve its
resources and the Agency’s deeper
analytic efforts for the actual risk
evaluation.
Low-Priority Substance designations
serve the same policy objectives.
Chemical substances with low hazard
and/or exposure potential that meet the
definition of Low-Priority Substances
are taken out of consideration for further
assessment. This gives the public notice
of chemical substances for which the
hazard and/or exposure potential is
anticipated to be low or nonexistent,
and provides some insight into which
chemical substances are likely not to
need additional evaluation and risk
management under TSCA. As a policy
matter, EPA is committed to making
Low-Priority designations on an ongoing
basis beyond the statutory minimum.
B. Scope of Designations
Consistent with the proposed rule,
EPA will designate the priority of a
‘‘chemical substance,’’ as a whole,
under this established process, and will
not limit its designation to a specific use
or subset of uses of a chemical
substance. The statute is clear that EPA
is to designate the priority of the
‘‘chemical substance’’—not a condition
of use for a chemical substance. See,
e.g., 15 U.S.C. 2605(b)(1)(A) (‘‘the
Administrator shall establish, by rule, a
risk-based screening process, including
criteria for designating chemical
substances as high-priority substances
for risk evaluations’’) (emphasis added);
2605(b)(1)(B) (definitions of high and
low priority chemical substances.)
Public comments on the proposed
rule were split with respect to this issue.
Some commenters suggested that EPA
should designate a specific use of a
chemical substance as High-Priority or a
Low-Priority. In general, these
commenters argued that EPA should
focus only on chemical ‘‘uses of greatest
concern,’’ in order to conserve EPA
resources, raising concern that EPA
would be unable to meet its statutory
deadlines by focusing so broadly. These
commenters argue that nothing in the
statute would foreclose this
interpretation, and that EPA’s reading of
the statute to require designation of
‘‘chemical substances’’ as either High or
Low-Priority is strained. One
commenter pointed to the ‘‘sentinel
exposure’’ provision in the risk
evaluation context as evidence that
Congress envisioned such a partial, usebased approach.
EPA disagrees that the statutory text
would support such an interpretation
for purposes of prioritization. The
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statute directs EPA to make
prioritization determinations on a
‘‘chemical substance’’ or ‘‘substance,’’
not on ‘‘uses,’’ see, e.g., 15 U.S.C.
2605(b)(1)(A)–(C), and in most cases,
without reference to ‘‘the conditions of
use.’’ Had Congress intended EPA to
designate individual uses as high or low
priority, the statute would have used a
different phrase or would have
otherwise clearly directed EPA to make
determinations on high or low priority
‘‘uses.’’ The clearest support for EPA’s
interpretation is found in the statutory
definitions of a High and Low Priority
Substance. Note, first, that these are
definitions of high and low priority
‘‘substances.’’ More critically, the
definitions themselves make clear that
Congress intended EPA to prioritize the
chemical as a whole, rather than to
prioritize particular uses or subsets of
uses. A High Priority substance is one
that presents ‘‘a potential hazard and a
potential route of exposure under the
conditions of use;’’ in other words, the
statute directs that the substance is High
Priority based on a potential risk from
a single one of the chemical’s various
conditions of use. Similarly, the statute
directs that EPA can only designate a
substance as low priority if ‘‘such
substance does not meet the standard
. . . for designating a chemical
substance a high-priority substance.’’
More generally, EPA believes the
addition of the phrase ‘‘the conditions of
use’’ (emphasis added) was intended to
move the Agency away from its past
practice of assessing only narrow uses of
a chemical substance, towards a more
inclusive approach to chemical
substance management. Note that the
phrase is plural, rather than singular
(conditions, not condition). While under
the definition of ‘‘conditions of use,’’
the Administrator retains some
discretion to ‘‘determine’’ the
conditions of use for each chemical
substance, that discretion is not
unfettered. As EPA interprets the
statute, the Agency is to exercise that
discretion consistent with the objective
of determining in a risk evaluation
whether a chemical substance—not just
individual uses or other individual
activities—presents an unreasonable
risk. In that regard, EPA will be guided
by its best understanding, based on
legislative text and history, of the
circumstances of manufacture,
processing, distribution in commerce,
use and disposal Congress intended
EPA to consider in risk evaluations.
However, this does not mean that in
prioritization, EPA will necessarily
consider every activity involving the
chemical substance to be a ‘‘condition of
use.’’ TSCA defines a chemical’s
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‘‘conditions of use’’ as ‘‘the
circumstances, as determined by the
Administrator, under which a chemical
substance is intended, known, or
reasonably foreseen to be manufactured,
processed, distributed in commerce,
used, or disposed of.’’ 15 U.S.C. 2602(4).
As discussed at greater length in the
final rule addressing procedures for
chemical risk evaluation under TSCA
(RIN 2070–AK20), published elsewhere
in this issue of Federal Register, based
on legislative history, statutory structure
and other evidence of Congressional
intent, EPA has determined that certain
activities generally should not be
considered to be ‘‘conditions of use.’’ 1
Thus early in the prioritization process,
EPA will identify the ‘‘circumstances’’
that constitute the ‘‘conditions of use’’
for each chemical substance. A
proposed determination would be
presented for public comment as part of
the proposed designation of the
substance as High- or Low-Priority.
Accordingly, those activities that the
Administrator determines fall within
the definition of ‘‘conditions of use’’
will be considered during prioritization.
When publishing proposed and final
priority designations pursuant to 40
CFR 702.9 and 40 CFR 702.11, the
Agency expects to identify the
information, analysis and basis used to
support the designations, as well as the
specific condition(s) of use that were the
basis for a High- or Low-Priority
designation. A chemical substance can
only be designated as a Low-Priority if
the ‘‘conditions of use’’ (as determined
by the Administrator) do not meet the
standard for High-Priority designation.
C. Timeframe
TSCA section 6(b)(1)(C) requires that
the prioritization process be completed
in no fewer than 9 months and no
greater than 12 months. Accordingly,
the final rule specifies that the
process—from initiation to final
designation—shall last between 9 and
12 months. EPA received no significant
comments on these timeframes, which
are statutorily mandated. However,
some commenters requested that EPA
clarify the points of initiation and
completion. Consistent with the
proposal, initiation of the prioritization
process, for purposes of this timeframe,
begins upon publication of a notice in
the Federal Register that identifies a
chemical substance for prioritization.
Similarly, the prioritization process is
complete upon publication of a notice
1 In the Risk Evaluation rule published elsewhere
in this issue of the Federal Register, EPA is
adopting other revisions that are applicable solely
to the risk evaluation process, based on statutory
provisions that are exclusive to risk evaluations.
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in the Federal Register announcing a
final priority designation. The
publication of a notice announcing a
final designation of a chemical as a
High-Priority Substance simultaneously
initiates a risk evaluation pursuant to
TSCA section 6(b)(4).
As indicated in the proposed rule,
this timeframe serves dual purposes.
The minimum 9-month timeframe
ensures that the general public;
potentially-affected industries; state,
tribal, and local governments;
environmental and health nongovernmental organizations; and others
have ample notice of upcoming federal
action on a given chemical substance,
and opportunity to engage with EPA
early in the process. The 12-month
maximum timeframe keeps the existing
chemical substances review pipeline in
a forward motion, and prevents EPA
from getting mired in analysis before
ever reaching the risk evaluation step.
D. Categories of Chemical Substances
TSCA section 26 provides EPA with
authority to take action on categories of
chemical substances. 15 U.S.C. 2625(c).
‘‘Category of Chemical Substances’’ is
defined at 15 U.S.C. 2625(c)(2)(A). EPA
is including in the final rule several
provisions from the proposal with
respect to categories of chemical
substances, without revision. EPA is
including, as proposed, a statement in
the regulation that nothing in the
subpart shall be construed as a
limitation on EPA’s authority to take
action with respect to categories of
chemical substances. Finally, several
commenters asked for clarification with
respect to how EPA might define a
category of chemical substances. EPA is
not adopting a regulatory definition of a
category, as the term is defined in TSCA
at 15 U.S.C. 2625(c)(2)(A). However,
should EPA determine to prioritize a
category of chemical substances, EPA
would describe the basis for such a
determination in the Federal Register
notice published to initiate
prioritization. As discussed elsewhere
in this preamble, EPA has revised the
regulation at 40 CFR 702.7(b) to state
that as part of the initiation notice, EPA
will provide an explanation of the
rationale for initiating the process on
the chemical substance, thus ensuring
the public has notice and an
opportunity to comment on any
decision to prioritize a category of
chemical substances.
As defined in 15 U.S.C. 2625(c), a
category of chemical substances means
a group of chemical substances the
members of which are similar in
molecular structure, in physical,
chemical or biological properties, in
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use, or in mode of entrance into the
human body or into the environment, or
the members of which are in some other
way suitable for classification as such
for purposes of this Act, except that
such term does not mean a group of
chemical substances which are grouped
together solely on the basis of their
being new chemical substances.
EPA proposed to include a
consideration of substitutes at the
candidate selection phase. This
consideration was deleted from the final
rule for the reasons discussed in Unit
IV(J).
E. Metals and Metal Compounds
A number of commenters expressed
concern that EPA may choose not to
apply the March 2007 Framework for
Metals Risk Assessment when
prioritizing metals or metal compounds.
The commenters were concerned that
metals and metal compounds have
unique attributes that are different from
organic and organometallic substances,
which necessitate special considerations
when assessing their human health and
ecological risks. TSCA mandates use of
the ‘‘Framework for Metals Risk
Assessment’’ to account for these
attributes. Commenters’ concerns stem
from a statement in EPA’s proposed rule
that it would consider ‘‘relevant
considerations’’ from this document ‘‘as
appropriate’’ when prioritizing
chemicals.
EPA fully recognizes the special
attributes and behaviors of metals and
metal compounds, and the mandate to
use the Framework document. EPA did
not intend the words ‘‘as appropriate’’
and ‘‘relevant considerations’’ to suggest
that EPA was seeking to avoid that
mandate or to otherwise diminish the
significance of those considerations.
Accordingly, EPA revised the final rule
to strike those words and eliminate the
confusion.
However, EPA notes that TSCA does
not contemplate completion of a full
risk assessment during the prioritization
phase. As the Metals Framework is
intended to guide EPA in conducting a
risk assessment on a metal or metal
compound, the phrase ‘‘as appropriate’’
was merely intended to reflect that no
risk assessment would be conducted at
this phase, and thus certain sections of
the Framework specific to conducting
risk assessments would not be relevant.
In the context of prioritization, EPA
interprets the Metals Framework
provision in TSCA to require EPA to
take into account the special attributes
and behaviors of metals and metal
compounds as described in the
Framework document. For example, the
document’s Key Principles discuss the
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differences between inorganic metals
and organic and organometallic
compounds, and the unique attributes,
properties, issues, and processes
associated with metals and metal
compounds. Nevertheless, to avoid
confusion, EPA has deleted the phrase
‘‘as appropriate’’ from the regulation.
F. Chemicals Subject to Prioritization
EPA is adopting these provisions from
the proposal without revision. Some
commenters encouraged EPA to exclude
certain groups of chemicals from
prioritization altogether, such as new
chemicals recently reviewed under
TSCA section 5 and ‘‘inactive’’
chemicals. Congress intended
prioritization to be a public and
transparent process of determining
which chemicals on the TSCA Inventory
deserve further evaluation. EPA does
not believe TSCA allows EPA to simply
exclude chemical substances from this
process. Chemical substances that do
not warrant risk evaluation would
instead be proposed as Low-Priority
Substances, and the public given an
opportunity to comment on that
determination through the procedures
in this final rule.
With respect to chemical substances
newly added to the TSCA Inventory
following EPA’s completion of premanufacture review under section 5 of
TSCA (15 U.S.C. 2604), EPA expects
that such chemical substances are not
likely to be selected as early HighPriority candidates in light of the riskrelated determination that the Agency
must make pursuant to TSCA section
5(a)(3). Chemicals that are designated as
‘‘inactive’’ pursuant to the Active/
Inactive Inventory rule (RIN 2070–
AK24) are still chemicals substances on
the TSCA Inventory, and therefore
subject to prioritization. Nothing in
TSCA prohibits EPA from initiating the
prioritization process on an ‘‘inactive’’
chemical substance and ultimately from
designating the priority of that chemical
substance. However, similar to chemical
substances newly added to the TSCA
Inventory, such chemicals may be less
likely to be selected as early HighPriority candidates. Whether or not a
chemical substance is actively
manufactured would generally be
relevant to informing EPA’s exposure
judgments during the prioritization
process.
G. Section 26 Scientific Standards
The proposed rule explained that EPA
did not need to specifically reference or
incorporate statutory requirements in
the proposed rule in order for them to
have effect. A number of commenters
opined on EPA’s lack of reference to the
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new scientific standards in section 26 of
TSCA. Some encouraged EPA to broadly
address how the new scientific terms
apply to prioritization decisions/
process, and to acknowledge the role of
section 26 in the prioritization process.
Commenters were split on whether and
how EPA should further define some of
these terms.
As a matter of practice, EPA has been,
and will continue to be, committed to
basing its decisions on the best available
science and the weight of the scientific
evidence. In response to public
comments on the proposal, EPA has
determined to make a number of
additions to the final rule to ensure that
the science standards in TSCA are more
explicitly incorporated into the
prioritization process. Specifically, the
final rule states that EPA’s proposed
priority designations under 40 CFR
702.9 and final priority designations
under 40 CFR 702.11 will be consistent
with the scientific standards in 15
U.S.C. 2625(h) and the weight of the
scientific evidence in 15 U.S.C. 2625(i).
These changes clarify that EPA’s
proposed and final designations for both
High- and Low-Priority Substances will
be consistent with TSCA’s new
requirements in section 26 related to
best available science and weight of the
scientific evidence.
H. Definitions
The final rule incorporates a number
of key definitions. As in the proposed
rule, the final rule includes a definition
of High-Priority Substances and LowPriority Substances. High-Priority
Substance means a chemical substance
that EPA determines, without
consideration of costs or other non-risk
factors, may present an unreasonable
risk of injury to health or the
environment because of a potential
hazard and a potential route of exposure
under the conditions of use, including
an unreasonable risk to potentially
exposed or susceptible subpopulations
identified as relevant by EPA. A LowPriority Substance means a chemical
substance that EPA concludes, based on
information sufficient to establish,
without consideration of costs or other
non-risk factors, does not meet the
standard for a High-Priority Substance.
EPA also incorporated the statutory
definition of conditions of use at 15
U.S.C. 2602(4). Conditions of use means
the circumstances, as determined by the
Administrator, under which a chemical
substance is intended, known, or
reasonably foreseen to be manufactured,
processed, distributed in commerce,
used, or disposed of.
EPA further incorporated the statutory
definition of potentially exposed or
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susceptible subpopulation at 15 U.S.C.
2602(12). Potentially exposed or
susceptible subpopulation means a
group of individuals within the general
population identified by the
Administrator who, due to either greater
susceptibility or greater exposure, may
be at greater risk than the general
population of adverse health effects
from exposure to a chemical substance
or mixture, such as infants, children,
pregnant women, workers, or the
elderly.
Finally, in response to comments that
favored a definition of ‘‘reasonably
available information,’’ EPA
incorporated the definition proposed in
EPA’s risk evaluation rule with some
modifications to be consistent with the
definition in the final risk evaluation
rule. In the final rule, reasonably
available information means
information that EPA possesses or can
reasonably generate, obtain and
synthesize for use, considering the
deadlines specified in TSCA section
6(b) for prioritization and risk
evaluation. Reasonably available
information includes information in
EPA’s possession that is confidential
business information under 15 U.S.C.
2613. Several commenters encouraged
EPA to take full advantage of its new
information gathering authorities and
not limit the basis of its decisions to
‘‘existing’’ information. EPA agrees that
it makes sense to view information that
can be obtained through testing as
‘‘reasonably available’’ in some
instances—especially information that
can be generated through short-term
testing, where it can be obtained within
the relevant statutory deadlines and the
information would be of sufficient value
to merit the testing. Thus, the final rule
modifies the definition of ‘‘reasonably
available information’’ to delete the
word ‘‘existing.’’ Note that EPA will, as
appropriate, also require longer-term
testing, and at times will need to do so
to more completely consider the hazard
characteristics and exposure pathways
of a chemical substance. However, EPA
does not think information that could be
generated through such testing should
be viewed as ‘‘reasonably available’’.
Ultimately, EPA will tailor its
information gathering efforts. Further,
the addition of the reference to
confidential business information was
intended to clarify that information in
EPA’s possession that is confidential
business information under 15 U.S.C.
2613 is also ‘‘reasonably available.’’
I. Pre-Prioritization Considerations
EPA received a significant number of
comments regarding the preprioritization phase (§ 702.5 in the
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proposed rule) included in the proposed
rule. As EPA noted in the proposal,
TSCA does not require EPA to articulate
in the prioritization rulemaking its
expected activities before prioritization,
including those related to information
gathering or putting chemicals into
some type of queue for input into the
prioritization pipeline. However, in an
attempt to be more transparent about
these expected activities, EPA included
in the proposal some considerations for
identifying both potential High- and
Low-Priority candidates, and general
hazard and exposure considerations.
While commenters generally
supported the concept and importance
of pre-prioritization activities, most took
issue with the level of detail and criteria
in EPA’s proposed rule and the
expected lack of transparency with
respect to EPA’s implementation, and
most expressed a strong desire to
increase public participation and
opportunities for comment during the
pre-prioritization phase. A number of
commenters stated that the Agency’s
proposed pre-prioritization process was
lacking sufficient detail, and that they
were not able to provide meaningful
comment. In short, the details of
implementing pre-prioritization
activities were the subject of widely
differing, and often irreconcilable views
by commenters.
For these reasons, EPA does not
believe it would be appropriate to
attempt to finalize a pre-prioritization
process without further discussions
with interested stakeholders. As such,
EPA has determined to defer a final
decision on the proposed preprioritization provisions as part of this
rule, and finalize at this time only the
prioritization process required under
TSCA. The Agency will promptly
initiate an additional stakeholder
process, to include an additional public
comment opportunity addressing EPA
pre-prioritization activities. EPA is fully
committed to further dialogue on best
practices for pre-prioritization activities,
and to carrying out these activities in a
transparent, science based manner, to
ensure successful implementation of the
prioritization and risk evaluation
processes.
Further, EPA appreciates the time
commenters spent developing and
sharing their views on this particular
subject. Commenters should rest
assured that these comments have been
informative to the Agency and will be
considered as EPA continues to
implement the recent amendments to
TSCA. EPA expects to re-engage the
public on this matter as early as Fall
2017, and these comments will serve as
a solid foundation for those discussions.
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Following the additional stakeholder
process, and in consideration of public
comments received, EPA will issue an
appropriate final action. While it is
premature to determine the outcome of
this future process, it could foreseeably
result in EPA formally establishing preprioritization procedures in a final
rule—either by first re-proposing, or by
finalizing based on the proposed rule.
Alternatively, for example, EPA may
issue a guidance document that further
describes the pre-prioritization process.
EPA will promptly evaluate public
comments received in response to the
additional stakeholder process and take
the appropriate next steps. In the
interim, the Agency fully expects to
move forward with prioritizing
chemicals in accordance with the
procedures of the final rule. Indeed,
TSCA compels the Agency to proceed
with designating a certain number of
chemicals as High- or Low-Priority by
December of 2019. 15 U.S.C.
2605(b)(2)(B). Pre-prioritization is not
statutorily mandated, and, as a legal
matter, not a necessary precursor to the
designation of High- and Low-Priority
substances. Pre-prioritization was
intended to be a phase of expected
activities (e.g., potential candidate
identification, information gathering/
review, etc.) to ensure a smooth process
of moving chemicals through the new
pipeline of prioritization, risk
evaluation, and (where warranted) risk
management. To illustrate, the Agency
could, as a general matter, draw
potential candidates for prioritization
from existing Agency resources
(including but not limited to, the 2014
update of the TSCA Work Plan for
Chemical Assessments (Ref. 3) and the
Safer Chemicals Ingredients List (Ref.
4)). However, until EPA takes final
action on pre-prioritization as discussed
above, the Agency will not follow a
formal process that identifies a chemical
as being ‘‘in pre-prioritization.’’
J. Information Availability
EPA expects to consider the existence
and availability of risk-related
information on a candidate chemical
substance before initiating the
prioritization process. EPA must
complete its prioritization process
within 12 months once prioritization
has been initiated for a chemical
substance, and then immediately
initiate a risk evaluation for a HighPriority Substance, and complete the
risk evaluation within three years of
initiation. As a general practice, EPA
intends to resolve any concerns it may
have about the sufficiency of
information about a given chemical
substance for purposes of prioritization,
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relative to the considerations in
§ 702.9(a), before subjecting that
chemical substance to the prioritization
process. Should EPA identify a critical
data need after the prioritization process
has already begun, it may be difficult or
impossible for the Agency to develop or
acquire the necessary information,
consistent with statutory deadlines for
prioritization. Although EPA will not
establish or implement a minimum
information requirement of broader
applicability, the Agency anticipates
that the types of information that are
helpful to inform and support
prioritization decisions will become
clearer as the Agency gains experience
with the prioritization process while
also allowing for advances in science
and information gathering.
Commenters argued that EPA should
not overuse its information gathering
authorities for a particular chemical
before that chemical has been identified
as a High-Priority Substance for risk
evaluation. To avoid confusion, EPA has
deleted several references to ensuring
sufficient information for purposes of
risk evaluation at the prioritization
stage. While EPA has broad authorities
to gather and require generation of
information, EPA did not intend to
suggest that it will routinely use its
information gathering authorities for a
particular chemical without first
evaluating the available information to
determine whether this is necessary.
EPA expects to review and consider the
reasonably available existing hazard and
exposure-related information, and
evaluate whether that information
would be sufficient to allow EPA to
complete the prioritization process
within the statutory deadlines. To the
extent the information is not currently
available or is insufficient, EPA will
determine on a case-by-case basis how
to best proceed to ensure that
information can be developed and
collected, reviewed and incorporated
into analyses and decisions in a timely
manner.
To further clarify this intent, EPA has
modified the final rule to indicate that
EPA generally expects to use a tiered
approach to information gathering. As a
general matter, a tiered approach to data
gathering first involves a review of
existing literature and available
information by EPA to determine data
needs. EPA is also mindful of its
requirements with respect to the
reduction of testing on vertebrate
animals under 15 U.S.C. 2603(h). For
identified data needs, EPA may issue a
voluntary call to the public for relevant
information or otherwise engage directly
with stakeholders, followed, as
necessary, by exercise of EPA’s
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authorities under TSCA to require
submission or generation of new data.
K. Candidate Selection
TSCA requires that EPA give
preference to chemical substances listed
in the 2014 update of the TSCA Work
Plan for Chemical Assessments that are
persistent and bioaccumulative; known
human carcinogens; and/or highly toxic.
TSCA section 6(b)(2)(B) further requires
that 50 percent of all ongoing risk
evaluations be drawn from the 2014
Update to the TSCA Work Plan for
Chemical Assessments, meaning that
EPA will need to draw at least 50
percent of High-Priority Substance
candidates from the same list. By
operation of this statutory directive, all
TSCA Work Plan chemical substances
will eventually be prioritized. These
preferences are incorporated into the
final rule during candidate selection at
40 CFR 702.5(c), without revision from
the proposal. Aside from these statutory
preferences, however, TSCA does not
specifically limit how EPA must
ultimately select a chemical substance
to put into the prioritization process.
As described in the proposed rule, in
practice, EPA expects to select for HighPriority Substances those chemicals
with the greatest hazard and exposure
potential first, consistent with the
policy objectives codified in 40 CFR
702.5(a). EPA has not revised the
regulatory text at 40 CFR 702.5(c) to
include additional preferences.
The proposed rule included a
statement that EPA is not required to
select candidates or initiate
prioritization pursuant to 40 CFR 702.9
in any ranked or hierarchical order. EPA
is striking this statement. Some
commenters encouraged EPA to adopt
such a system and EPA is retaining the
discretion to do so by rule in the future.
EPA does not believe the statement in
the proposed rule was necessary or had
any legal effect, since nothing in the
rule or TSCA requires EPA to
implement an ordering or ranking
system in selecting candidate chemical
substances for prioritization.
The proposed rule included a general
objective for identifying candidates for
High-Priority Substances. In response to
comments that EPA more explicitly
recognize Low-Priority designations as
part of the process, the final rule now
includes a general objective for selecting
candidates for Low-Priority, consistent
with the statutory definition for LowPriority Substances. As defined in
TSCA, Low-Priority Substances are
those for which risk evaluation is not
warranted at this time. 15 U.S.C.
2605(b)(1)(A). As described in the final
rule, EPA will seek to identify
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candidates for Low-Priority designation
where the information on hazard and
exposure under the conditions of use for
the chemical substance is sufficient to
establish that a risk evaluation is not
warranted to determine whether the
chemical substance presents an
unreasonable risk of injury to health or
the environment, including an
unreasonable risk to potentially exposed
or susceptible subpopulations identified
as relevant by EPA.
EPA included in its proposed rule a
general statement that EPA ‘‘may
consider the relative hazard and
exposure of potential candidate’s
substitutes’’ in selecting a chemical for
prioritization. Some commenters believe
strongly that EPA should not consider
substitutes as part of the prioritization
phase because it is a consideration more
appropriate for the risk management
phase. Others had concern that
considering the relative risk of
substitutes had the potential to lead to
unlawful consideration of the
availability of substitutes at this phase—
a non-risk factor the commenters assert
is expressly excluded from
consideration during the prioritization
process. Several commenters expressed
general support for consideration of
substitutes to the extent that it could
help to avoid regrettable substitution,
and conserve both Agency and industry
time and resources that would result
from inappropriate switches to other
dangerous chemicals. EPA has stricken
the provision in question from the final
rule. EPA agrees that the consideration
of alternatives is most appropriately
considered as part of any risk
management rule.
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L. Initiation of Prioritization
The prioritization process officially
begins, for purposes of triggering the 9
to 12-month statutory timeframe, when
EPA publishes a notice in the Federal
Register identifying a chemical
substance for prioritization. The final
rule includes a new provision clarifying
that EPA generally expects to provide an
explanation in this notice for why it
chose to initiate the process for the
particular chemical substance (e.g.,
whether EPA views this as a potential
candidate for High or Low priority).
This was in response to commenters’
concerns that initiation of the
prioritization process could send strong
signals to the public regarding potential
risks, even if certain uses of that
chemical did not prompt the initiation
of prioritization. Note that a proposed
priority designation, as EPA clarified in
the final rule, is not a finding of
unreasonable risk by the Agency.
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Publication of the notice in the
Federal Register also initiates a 90-day
public comment period. For each
chemical substance, EPA will open a
docket to facilitate receipt of public
comments and access to publicly
available information throughout this
process. Interested persons are welcome
and encouraged during this time to
submit information relevant to the
chemical substance. Because TSCA
specifically requires the prioritization
process to be risk-based and EPA’s
determinations to exclude non-risk
factors, relevant information at this
stage is limited to that which is riskrelated.
Although the proposed rule specified
that EPA would publish the results of
the screening review in this same
notice, EPA’s final rule shifts the timing
of the screening review, which will now
occur after the close of this initial 90day public comment period. A number
of commenters expressed concern that
the proposed rule did not guarantee any
opportunity for public comment prior to
the screening review, and many felt
strongly that the Agency needed to
engage the public to inform
prioritization decisions. The shift in
timing puts the screening review
squarely within the prioritization
process and affords the public an
opportunity to inform EPA’s screening
review before that review. Thus,
commenters are encouraged to submit
relevant information that may inform
EPA’s screening review. EPA will
consider all relevant information
received during this comment period.
M. Screening Review
Following completion of the initial
90-day public comment period, EPA
will screen the selected candidate
against the specific criteria and
considerations in TSCA section
6(b)(1)(A). Those criteria and
considerations are: (1) The chemical
substance’s hazard and exposure
potential; (2) the chemical substance’s
persistence and bioaccumulation; (3)
potentially exposed or susceptible
subpopulations; (4) storage of the
chemical substance near significant
sources of drinking water; (5) the
chemical substance’s conditions of use
or significant changes in conditions of
use; and (6) the chemical substance’s
production volume or significant
changes in production volume. The
Agency will develop guidance,
consistent with OMB’s Final Bulletin for
Agency Good Guidance Practices (72 FR
3432, January 25, 2007), to describe the
implications of the criteria and
considerations and to explain how EPA
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generally expects to apply them during
the screening review step.
The final rule also includes an
additional criterion, consistent with the
proposal: (7) Other risk-based criteria
that EPA determines to be relevant to
the designation of the chemical
substance’s priority. As explained in the
proposal, this final criterion allows the
screening review to adapt with future
changes in our understanding of science
and chemical risks. Should EPA rely on
this criterion to support a proposed
designation, EPA would describe in the
publication of proposed designation the
specific factors considered for such
designation, thereby affording the
public notice and an opportunity to
comment on the basis for the proposed
designation under this criterion. The
screening review is not a risk
evaluation, but rather a review of
reasonably available information on the
chemical substance that relates to the
screening criteria. EPA expects to
review all sources of relevant
information, consistent with the
scientific standards in 15 U.S.C.
2625(h), while conducting the screening
review.
N. Proposed Designation
Based on the results of the screening
review, EPA will propose to designate
the chemical substance as either a HighPriority Substance or Low-Priority
Substance, as those terms are defined in
40 CFR 702.3. In making this proposed
designation, as directed by the statute,
EPA will not consider costs or other
non-risk factors.
The final rule provides that EPA will
publish the proposed designation in the
Federal Register, along with an
identification of the information,
analysis and basis used to support a
proposed designation. Pursuant to 15
U.S.C. 2625(j), EPA shall make this
information available to the public in
the docket, subject to 15 U.S.C. 2613.
Publication of this notice begins a
second period of public comment for 90
days, during which time the public may
submit comments on EPA’s proposed
designation. EPA will reopen the same
docket opened upon initiation of the
prioritization process to facilitate
receipt of comments and information.
Because the supporting documentation
for a proposed High-Priority Substance
designation is likely to foreshadow what
will go into a scoping document for risk
evaluation, EPA will be particularly
interested in comments on the accuracy
of scope-related information such as the
chemical’s ‘‘conditions of use,’’ at this
step.
In the event of insufficient
information at the proposed designation
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step, the proposed rule required EPA to
propose to designate the chemical as a
High-Priority Substance. A number of
commenters felt that a ‘‘default’’ to
High-Priority Substance would be an
unfair result for affected industries and/
or irresponsible action by the Agency.
This provision has largely been stricken
from the final rule, except for the
circumstance that is explicitly required
in 15 U.S.C. 2505(b)(1), which is now
described in 40 CFR 702.9(e). TSCA
requires that the prioritization process
lead to one of two outcomes by the end
of the 12-month deadline: A HighPriority Substance designation or a LowPriority Substance designation. 15
U.S.C. 2605(b)(1)(B). On further
consideration, EPA believes the Agency
is charged by the statute, and will be
able, to determine which of these
priority categories each chemical falls
into during the prioritization process,
and therefore it is not necessary or
appropriate to establish a default. EPA
notes that the statute specifically
prohibits a default to Low-Priority,
requiring that a Low-Priority Substance
designation be based on ‘‘information
sufficient to establish’’ that a chemical
substance meets the definition. 15
U.S.C. 2605(b)(1)(B)(ii). There is no
comparable statutory requirement for
High-Priority Substance designations.
15 U.S.C. 2605(b)(1)(B)(i).
In response to a number of concerns
raised by public commenters, EPA is
striking the ‘‘issue preclusion’’
provision related to proposed
designations as Low-Priority
Substances, which stated that all
comments that could be raised on the
issues in the proposed designation must
be presented during the comment
period, or would be considered waived
and could not form the basis for an
objection or challenge in any
subsequent administrative or judicial
proceeding. Under general principles of
administrative law, commenters are
required to identify relevant available
information and raise objections that
could be raised during established
comment periods, and courts generally
will require commenters to have done
so as a matter of exhaustion of
administrative remedies. EPA has
concluded that these principles provide
sufficient assurance that commenters
will raise timely objections and provide
timely information and has therefore
decided to strike the proposed
regulatory text.
Although the final rule makes other
clarifications to the ‘‘Proposed Priority
Designation’’ provision, the standard for
designating High- and Low-Priority
Substances has not changed from the
proposed rule. EPA will prioritize a
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‘‘chemical substance,’’ and the standard
for a High-Priority Substance (‘‘. . . may
present an unreasonable risk [. . .]
because of a potential hazard and a
potential route of exposure . . .’’) can
be met by identification of one or more
condition of use that meet that standard.
Conversely, in designating a LowPriority Substance (‘‘. . . based on
sufficient information, such substance
does not meet the standard for [. . .] a
high-priority substance . . .’’), TSCA
requires EPA to determine that under
none of the conditions of use, as
determined by the Administrator, does
the chemical substance meet the
definition of a High-Priority Substance.
O. Final Priority Designation
The last step in the prioritization
process is for EPA to finalize its
designation of a chemical substance as
either a High-Priority Substance or a
Low-Priority Substance. EPA will
consider additional relevant information
received during the proposed
designation step before finalizing a
priority designation, excluding any
consideration of costs or other non-risk
factors. The final rule specifies that EPA
will publish a notice of the final priority
designation in the Federal Register,
using the same docket that was used for
the initiation and proposal steps.
EPA has included additional
regulatory text in the final rule,
clarifying that EPA would publish an
identification of information, analysis,
and basis used to support the final
designation, as required under TSCA.
Additionally, EPA amended the
proposed rule to provide that EPA
generally expects to identify which
condition(s) of use were the primary
bases for the priority designation. This
was made in response to some concerns
that a priority designation for a
chemical substance could send strong
signals to the public regarding potential
risks.
P. Repopulation of High-Priority
Substances
TSCA requires EPA to finalize a
designation for at least one new HighPriority Substance upon completion of a
risk evaluation for another chemical
substance, other than a risk evaluation
that was requested by a manufacturer.
Because the timing for the completion of
risk evaluation and/or the prioritization
process will be difficult to predict, EPA
intends to satisfy this 1-off, 1-on
replacement obligation as follows: In the
notice published in the Federal Register
finalizing the designation of a new
High-Priority Substance, EPA generally
expects to identify the complete or nearcomplete risk evaluation that the new
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High-Priority Substance will replace. So
long as the designation occurs within a
reasonable time before or after the
completion of the risk evaluation, this
will satisfy Congress’ intent while
avoiding unnecessary delay and the
logistical challenges that would be
associated with more perfectly aligning
a High-Priority Substance designation
with the completion of a risk evaluation.
A few commenters suggested that EPA
define a ‘‘reasonable time’’ for these
purposes. Commenters expressed
concern that, in the absence of a defined
period of time, a completed risk
evaluation may never be replaced with
a new High-Priority Substance, slowing
the pace of EPA’s overall progress
towards reviewing the backlog of
existing chemicals. EPA has determined
not to include a specific time frame in
the regulation that may be too
prescriptive to implement. However, as
a general matter, EPA expects to
designate a new High-Priority Substance
no later than 45 days following
completion of a risk evaluation.
Q. Effect of Final Priority Designation
Final designation of a chemical
substance as a High-Priority Substance
requires EPA to immediately begin a
risk evaluation on that chemical
substance. Final designation of a
chemical substance as a Low-Priority
Substance is a final agency action that
means that a risk evaluation of the
chemical substance is not warranted at
the time. This does not preclude EPA
from later revising the designation, if
warranted. EPA has added a provision
in the final rule clarifying that a final
priority designation is neither a finding
of unreasonable risk to health or the
environment, nor a finding of no
unreasonable risk.
A Low-Priority Substance designation
is explicitly subject to judicial review.
15 U.S.C. 2618(a)(1)(C). A High-Priority
Substance designation is not a final
agency action and is not subject to
judicial review. Rather, a High-Priority
Substance designation prompts the
initiation of a risk evaluation. 15 U.S.C.
2605(b)(4). Upon the conclusion of such
a risk evaluation, EPA may determine
that a chemical substance does not
present an unreasonable risk of injury to
human health or the environment under
the conditions of use. Such a
determination must be issued in an
order, and is a final agency action
subject to judicial review. 15 U.S.C.
2605(i). If EPA conversely determines
that a chemical substance presents an
unreasonable risk of injury to human
health or the environment under the
conditions of use, that determination is
not a final agency action and is not
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subject to judicial review. TSCA
mandates that the Agency must issue a
rule to apply certain requirements so
that the chemical substance or mixture
no longer presents the unreasonable
risk. 15 U.S.C. 2605(a). Such a final rule
is a final agency action and is subject to
judicial review.
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R. Revision of Designation
TSCA provides that EPA may revise a
final designation of a chemical
substance from a Low-Priority
Substance to a High-Priority Substance
at any time based on information that is
reasonably available to the Agency. The
final rule outlines the process the
Agency will take to revise such a
designation. Essentially, the revision
process involves restarting the
prioritization process, and applying the
provisions in the same way they would
apply to a chemical that has not been
previously prioritized.
TSCA does not require a process for
revising a High-Priority Substance to a
Low-Priority, and the final rule does not
provide for such revision. This is for
good reason. Prioritization serves a
limited purpose: To identify chemicals
for further evaluation. Once a chemical
has been identified as a High-Priority
Substance, the risk evaluation begins,
the priority designation of the chemical
having served its purpose, and EPA is
compelled to complete that risk
evaluation within a statutory 3-year
deadline. Moreover, because the risk
evaluation is already underway at this
point, EPA believes it would not make
sense to revisit whether or not a risk
evaluation is warranted. EPA believes
Congress intended EPA to see the risk
evaluation process through to its
conclusion and to make a finding under
15 U.S.C. 2605(i) that the substance
does not pose an unreasonable risk, not
to revise a priority designation.
S. Small Business Outreach
A few commenters recommended that
EPA conduct targeted outreach to small
businesses early in the process of
prioritization to identify impacts to
small businesses. Commenters suggest
that the small business community
could benefit from background
information on EPA’s activities, while
EPA could receive valuable input from
relevant small businesses.
EPA welcomes the opportunity to
engage with small businesses that may
use the subject chemical during the
prioritization process, particularly
during the two 90-day public comment
periods built into the prioritization
procedural rule, and will provide
current information about these
activities through the Agency’s Web site
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19:37 Jul 19, 2017
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at https://www.epa.gov/assessing-andmanaging-chemicals-under-tsca. EPA
also expects to work closely with its
federal partners at the Small Business
Administration, Office of Advocacy as a
means to engage with the small business
community. TSCA mandates that both
the prioritization and risk evaluation
processes be risk-based. As such, EPA
would be most interested in learning
from small businesses and other
stakeholders about a particular
chemical’s uses, and potential hazards
and exposures. Economic impacts of
any potential future regulation have an
important role during the consideration
of risk management measures, if and
when warranted, but TSCA explicitly
excludes consideration of these impacts
during prioritization and risk evaluation
actions.
V. References
The following is a listing of the
documents that are specifically
referenced in this document. The docket
includes these documents and other
information considered by EPA,
including documents that are referenced
within the documents that are included
in the docket, even if the referenced
document is not physically located in
the docket. For assistance in locating
these other documents, please consult
the technical person listed under FOR
FURTHER INFORMATION CONTACT.
1. EPA. Procedures for Prioritization of
Chemicals for Risk Evaluation Under the
Toxic Substances Control Act; Proposed
Rule. Federal Register (82 FR 4825,
January 17, 2017) (FRL–9957–74).
2. EPA. Procedures for Prioritization of
Chemicals for Risk Evaluation under
TSCA: Response to Public Comments;
SAN 5943; RIN 2070–AK23; EPA–HQ–
OPPT–2016–0636. 2017.
3. EPA. TSCA Work Plan for Chemical
Assessments: 2014 Update. October
2014. Available online at: https://
www.epa.gov/sites/production/files/
2015-01/documents/tsca_work_plan_
chemicals_2014_update-final.pdf.
4. EPA. Safer Chemical Ingredients List
(SCIL). Available online at: https://
www.epa.gov/saferchoice/saferingredients. See also Master Criteria,
September 2012, Version 2.1, available
online at: https://www.epa.gov/sites/
production/files/2013-12/documents/
dfe_master_criteria_safer_ingredients_
v2_1.pdf.
VI. Statutory and Executive Order
Reviews
Additional information about these
statutes and Executive Orders can be
found at https://www2.epa.gov/lawsregulations/laws-and-executive-orders.
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33761
A. Executive Order 12866: Regulatory
Planning and Review and Executive
Order 13563: Improving Regulation and
Regulatory Review
This action is a significant regulatory
action that was submitted to the Office
of Management and Budget (OMB) for
review under Executive Orders 12866
(58 FR 51735, October 4, 1993) and
13563 (76 FR 3821, January 21, 2011).
Any changes made in response to OMB
recommendations have been
documented in the docket. This action
is not subject to the requirements of
Executive Order 13771, entitled
Reducing Regulation and Controlling
Regulatory Costs (82 FR 9339, February
3, 2017), because this action does not
impose any costs.
B. Paperwork Reduction Act (PRA)
This action does not contain any
information collection activities that
require approval under the PRA, 44
U.S.C. 3501 et seq. This rulemaking
addresses internal EPA operations and
procedures and does not impose any
requirements on the public.
C. Regulatory Flexibility Act (RFA)
I certify under section 605(b) of the
RFA, 5 U.S.C. 601 et seq., that this
action will not have a significant
economic impact on a substantial
number of small entities. This
rulemaking addresses internal EPA
operations and procedures and does not
impose any requirements on the public,
including small entities.
D. Unfunded Mandates Reform Act
(UMRA)
This action does not contain any
unfunded mandate as described in
UMRA, 2 U.S.C. 1531–1538, and does
not significantly or uniquely affect small
governments. The action imposes no
enforceable duty on any state, local or
tribal governments or the private sector.
E. Executive Order 13132: Federalism
This action does not have federalism
implications as specified in Executive
Order 13132 (64 FR 43255, August 10,
1999). It will not have substantial direct
effects on the states, on the relationship
between the national government and
the states, or on the distribution of
power and responsibilities among the
various levels of government.
F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
This action does not have tribal
implications as specified in Executive
Order 13175 (65 FR 67249, November 9,
2000). It will not have substantial direct
effects on one or more Indian tribes, on
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the relationship between the Federal
Government and Indian tribes, or on the
distribution of power and
responsibilities between the Federal
Government and Indian tribes. Thus,
Executive Order 13175 does not apply
to this action.
G. Executive Order 13045: Protection of
Children From Environmental Health
Risks and Safety Risks
EPA interprets Executive Order 13045
(62 FR 19885, April 23, 1997) as
applying only to those regulatory
actions that concern environmental
health or safety risks that the EPA has
reason to believe may
disproportionately affect children, per
the definition of ‘‘covered regulatory
action’’ in section 2–202 of the
Executive Order. This action is not
subject to Executive Order 13045
because it does not concern an
environmental health risk or safety risk.
H. Executive Order 13211: Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution, or Use
This action is not a ‘‘significant
energy action’’ as defined in Executive
Order 13211 (66 FR 28355, May 22,
2001), because it is not likely to have a
significant adverse effect on the supply,
distribution or use of energy. This
rulemaking addresses internal EPA
operations and procedures and does not
impose any requirements on the public.
I. National Technology Transfer and
Advancement Act (NTTAA)
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J. Executive Order 12898: Federal
Actions To Address Environmental
Justice in Minority Populations and
Low-Income Populations
This action does not establish an
environmental health or safety standard,
and is therefore not is not subject to
environmental justice considerations
under Executive Order 12898 (59 FR
7629, February 16, 1994). This
rulemaking addresses internal EPA
operations and procedures and does not
have any impact on human health or the
environment.
VII. Congressional Review Act (CRA)
This rule is exempt from the CRA, 5
U.S.C. 801 et seq., because it is a rule
of agency organization, procedure or
practice that does not substantially
affect the rights or obligations of nonagency parties.
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Environmental protection, Chemical
substances, Chemicals, Hazardous
substances, Health and safety,
Prioritization, Screening, Toxic
substances.
Dated: June 22, 2017.
E. Scott Pruitt,
Administrator.
Therefore, 40 CFR chapter I,
subchapter R, is amended as follows:
PART 702—GENERAL PRACTICES
AND PROCEDURES
1. The authority citation for part 702
is revised to read as follows:
■
Authority: 15 U.S.C. 2605 and 2619.
■
2. Add subpart A to read as follows:
Subpart A—Procedures for Prioritization of
Chemical Substances for Risk Evaluation
Sec.
702.1 General provisions.
702.3 Definitions.
702.4 [Reserved]
702.5 Candidate selection.
702.7 Initiation of prioritization process.
702.9 Screening review and proposed
priority designation.
702.11 Final priority designation.
702.13 Revision of designation.
702.15 Effect of designation as a lowpriority substance.
702.17 Effect of designation as a highpriority substance.
Subpart A—Procedures for
Prioritization of Chemical Substances
for Risk Evaluation
§ 702.1
This rulemaking does not involve any
technical standards, and is therefore not
subject to considerations under NTTAA
section 12(d), 15 U.S.C. 272 note.
VerDate Sep<11>2014
List of Subjects in 40 CFR Part 702
General provisions.
(a) Purpose. This regulation
establishes the risk-based screening
process for designating chemical
substances as a High-Priority Substance
or a Low-Priority Substance for risk
evaluation as required under section
6(b) of the Toxic Substances Control
Act, as amended (15 U.S.C. 2605(b)).
(b) Scope of designations. EPA will
make priority designations pursuant to
these procedures for a chemical
substance, not for a specific condition or
conditions of uses of a chemical
substance.
(c) Categories of chemical substances.
Nothing in this subpart shall be
interpreted as a limitation on EPA’s
authority under 15 U.S.C. 2625(c) to
take action, including the actions
contemplated in this subpart, on a
category of chemical substances.
(d) Prioritization timeframe. The
Agency will publish a final priority
designation for a chemical substance in
no fewer than 9 months and no longer
than 1 year following initiation of
prioritization pursuant to § 702.7.
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(e) Metals or metal compounds. EPA
will identify priorities for chemical
substances that are metals or metal
compounds in accordance with 15
U.S.C. 2605(b)(2)(E).
(f) Applicability. These regulations do
not apply to any chemical substance for
which a manufacturer requests a risk
evaluation under 15 U.S.C.
2605(b)(4)(C).
(g) Scientific standards and weight of
the scientific evidence. EPA’s proposed
priority designations under § 702.9 and
final priority designations under
§ 702.11 will be consistent with the
scientific standards provision in 15
U.S.C. 2625(h) and the weight of the
scientific evidence provision in 15
U.S.C. 2625(i).
(h) Interagency collaboration. EPA
will consult with other relevant Federal
Agencies during the administration of
this subpart.
§ 702.3
Definitions.
For purposes of this subpart, the
following definitions apply:
Act means the Toxic Substances
Control Act, as amended (15 U.S.C.
2601 et seq.).
Conditions of use means the
circumstances, as determined by the
Administrator, under which a chemical
substance is intended, known, or
reasonably foreseen to be manufactured,
processed, distributed in commerce,
used, or disposed of.
EPA means the U.S. Environmental
Protection Agency.
High-priority substance means a
chemical substance that EPA
determines, without consideration of
costs or other non-risk factors, may
present an unreasonable risk of injury to
health or the environment because of a
potential hazard and a potential route of
exposure under the conditions of use,
including an unreasonable risk to
potentially exposed or susceptible
subpopulations identified as relevant by
EPA.
Low-priority substance means a
chemical substance that EPA concludes,
based on information sufficient to
establish, without consideration of costs
or other non-risk factors, does not meet
the standard for a High-Priority
Substance.
Potentially exposed or susceptible
subpopulation means a group of
individuals within the general
population identified by the
Administrator who, due to either greater
susceptibility or greater exposure, may
be at greater risk than the general
population of adverse health effects
from exposure to a chemical substance
or mixture, such as infants, children,
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pregnant women, workers, or the
elderly.
Reasonably available information
means information that EPA possesses
or can reasonably generate, obtain and
synthesize for use, considering the
deadlines specified in 15 U.S.C. 2605(b)
for prioritization and risk evaluation.
Information that meets such terms is
reasonably available information
whether or not the information is
confidential business information that is
protected from public disclosure under
15 U.S.C. 2613.
[Reserved]
§ 702.5
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§ 702.4
Candidate selection.
(a) General objective. In selecting
candidates for a High-Priority Substance
designation, it is EPA’s general objective
to select those chemical substances with
the greatest hazard and exposure
potential first, considering reasonably
available information on the relative
hazard and exposure of potential
candidates. In selecting candidates for
Low-Priority Substance designation, it is
EPA’s general objective to select those
chemical substances with hazard and/or
exposure characteristics under the
conditions of use such that a risk
evaluation is not warranted at the time
to determine whether the chemical
substance presents an unreasonable risk
of injury to health or the environment,
including an unreasonable risk to
potentially exposed or susceptible
subpopulations identified as relevant by
EPA.
(b) Available information. EPA
expects to ensure that there is
reasonably available information to
meet the deadlines for prioritization
under the Act.
(c) Preferences and TSCA work plan.
In selecting a candidate for
prioritization as a High-Priority
Substance, EPA will:
(1) Give preference to:
(i) Chemical substances that are listed
in the 2014 update of the TSCA Work
Plan for Chemical Assessments as
having a persistence and
bioaccumulation score of 3; and
(ii) Chemical substances that are
listed in the 2014 update of the TSCA
Work Plan for Chemical Assessments
that are known human carcinogens and
have high acute and chronic toxicity;
and
(2) Identify a sufficient number of
candidates from the 2014 update of the
TSCA Work Plan for Chemical
Assessments to ensure that, at any given
time, at least 50 percent of risk
evaluations being conducted by EPA are
drawn from that list until all substances
on the list have been designated as
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either a High-Priority Substance or LowPriority Substance pursuant to § 702.11.
(d) Purpose. The purpose of the
preferences and criteria in paragraphs
(a) through (c) of this section is to
inform EPA’s decision whether or not to
initiate the prioritization process
pursuant to § 702.7, and the proposed
designation of the chemical substance as
either a High-Priority Substance or a
Low-Priority Substance pursuant to
§ 702.9.
(e) Insufficient information. If EPA
believes it would not have sufficient
information for purposes of
prioritization, EPA generally expects to
obtain the information necessary to
inform prioritization prior to initiating
the process pursuant to § 702.9, using
voluntary means of information
gathering and, as necessary, exercising
its authorities under the Act in
accordance with the requirements of 15
U.S.C. 2603, 15 U.S.C. 2607, and 15
U.S.C. 2610. In exercising its authority
under 15 U.S.C. 2603(a)(2), EPA will
identify the need for the information in
accordance with 15 U.S.C. 2603(a)(3).
§ 702.7
Initiation of prioritization process.
(a) EPA generally expects to initiate
the prioritization process for a chemical
substance only when it believes that the
information necessary to prioritize the
substance is reasonably available.
(b) EPA will initiate prioritization by
publishing a notice in the Federal
Register identifying a chemical
substance for prioritization. EPA will
include a general explanation in this
notice for why it chose to initiate the
process on the chemical substance.
(c) The prioritization timeframe in
§ 702.1(d) begins upon EPA’s
publication of the notice described in
paragraph (b) of this section.
(d) Publication of the notice in the
Federal Register pursuant to paragraph
(b) of this section will initiate a period
of 90 days during which interested
persons may submit relevant
information on that chemical substance.
Relevant information might include, but
is not limited to, any information that
may inform the screening review
conducted pursuant to § 702.9(a). EPA
will open a separate docket for each
chemical substance to facilitate receipt
of information.
(e) EPA may, in its discretion, extend
the public comment period in paragraph
(d) of this section for up to three months
in order to receive or evaluate
information submitted under 15 U.S.C.
2603(a)(2)(B). The length of the
extension will be based upon EPA’s
assessment of the time necessary for
EPA to receive and/or evaluate
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33763
information submitted under 15 U.S.C.
2603(a)(2)(B).
§ 702.9 Screening review and proposed
priority designation.
(a) Screening review. Following the
close of the comment period described
in § 702.7(d), including any extension
pursuant to paragraph (e) of that section,
EPA will generally use reasonably
available information to screen the
candidate chemical substance against
the following criteria and
considerations:
(1) The chemical substance’s hazard
and exposure potential;
(2) The chemical substance’s
persistence and bioaccumulation;
(3) Potentially exposed or susceptible
subpopulations;
(4) Storage of the chemical substance
near significant sources of drinking
water;
(5) The chemical substance’s
conditions of use or significant changes
in conditions of use;
(6) The chemical substance’s
production volume or significant
changes in production volume; and
(7) Other risk-based criteria that EPA
determines to be relevant to the
designation of the chemical substance’s
priority.
(b) Information sources. In conducting
the screening review in paragraph (a) of
this section, EPA expects to consider
sources of information relevant to the
listed criteria and consistent with the
scientific standards provision in 15
U.S.C. 2625(h), including, as
appropriate, sources for hazard and
exposure data listed in Appendices A
and B of the TSCA Work Plan
Chemicals: Methods Document
(February 2012).
(c) Proposed designation. Based on
the results of the screening review in
paragraph (a) of this section, relevant
information received from the public as
described in § 702.7(d), and other
information as appropriate and
consistent with 15 U.S.C. 2625(h) and
(i), EPA will propose to designate the
chemical substance as either a HighPriority Substance or Low-Priority
Substance, along with an identification
of the information, analysis, and basis
used to support the proposed
designation.
(d) Costs and non-risk factors. EPA
will not consider costs or other non-risk
factors in making a proposed priority
designation.
(e) Insufficient information. If
information remains insufficient to
enable the proposed designation of the
chemical substance as a Low-Priority
Substance after any extension of the
initial public comment period pursuant
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to § 702.7(e), EPA will propose to
designate the chemical substance as a
High-Priority Substance.
(f) Conditions of use. EPA will
propose to designate a chemical
substance as a High-Priority Substance
based on the proposed conclusion that
the chemical substance satisfies the
definition of High-Priority Substance in
§ 702.3 under one or more activities that
the Agency determines constitute
conditions of use. EPA will propose to
designate a chemical substance as a
Low-Priority Substance based on the
proposed conclusion that the chemical
substance meets the definition of LowPriority Substance in § 702.3 under the
activities that the Agency determines
constitute conditions of use.
(g) Publication. EPA will publish the
proposed designation in the Federal
Register, along with an identification of
the information, analysis and basis used
to support a proposed designation, in a
form and manner that EPA deems
appropriate, and provide a comment
period of 90 days, during which time
the public may submit comment on
EPA’s proposed designation. EPA will
open a docket to facilitate receipt of
public comment.
Low-Priority Substance consistent with
15 U.S.C. 2625(h) and (i).
(b) EPA will not consider costs or
other non-risk factors in making a final
priority designation.
(c) EPA will publish each final
priority designation in the Federal
Register, along with an identification of
the information, analysis, and basis
used to support a final designation
consistent with 15 U.S.C. 2625(h), (i)
and (j). For High-Priority Substance
designations, EPA generally expects to
indicate which condition(s) of use were
the primary basis for such designations.
(d) As required in 15 U.S.C.
2605(b)(3)(C), EPA will finalize a
designation for at least one High-Priority
Substance for each risk evaluation it
completes, other than a risk evaluation
that was requested by a manufacturer
pursuant to subpart B of this part. The
obligation in 15 U.S.C. 2605(b)(3)(C)
will be satisfied by the designation of at
least one High-Priority Substance where
such designation specifies the risk
evaluation that the designation
corresponds to, and where the
designation occurs within a reasonable
time before or after the completion of
the risk evaluation.
§ 702.13
§ 702.11
Final priority designation.
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(a) After considering any additional
information collected from the proposed
designation process in § 702.9, as
appropriate, EPA will finalize its
designation of a chemical substance as
either a High-Priority Substance or a
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Revision of designation.
EPA may revise a final designation of
a chemical substance from Low-Priority
to High-Priority Substance at any time
based on reasonably available
information. To revise such a
designation, EPA will re-initiate the
prioritization process on that chemical
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Sfmt 9990
substance in accordance with § 702.7,
re-screen the chemical substance and
propose a priority designation pursuant
to § 702.9, and finalize the priority
designation pursuant to § 702.11.
§ 702.15 Effect of designation as a lowpriority substance.
Designation of a chemical substance
as a Low-Priority Substance under
§ 702.11 means that a risk evaluation of
the chemical substance is not warranted
at the time, but does not preclude EPA
from later revising the designation
pursuant to § 702.13, if warranted.
Designation as a Low-Priority Substance
is not a finding that the chemical
substance does not present an
unreasonable risk, but rather that it does
not meet the High-Priority Substance
definition.
§ 702.17 Effect of designation as a highpriority substance.
Final designation of a chemical
substance as a High-Priority Substance
under § 702.11 initiates a risk evaluation
pursuant to subpart B of this part.
Designation as a High-Priority
Substance is not a final agency action
and is not subject to judicial review
until the date of promulgation of the
associated final rule under section 6(a).
Designation as a High-Priority
Substance is not a finding that the
chemical substance presents an
unreasonable risk.
[FR Doc. 2017–14325 Filed 7–19–17; 8:45 am]
BILLING CODE 6560–50–P
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Agencies
[Federal Register Volume 82, Number 138 (Thursday, July 20, 2017)]
[Rules and Regulations]
[Pages 33753-33764]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-14325]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 702
[EPA-HQ-OPPT-2016-0636; FRL-9964-24]
RIN 2070-AK23
Procedures for Prioritization of Chemicals for Risk Evaluation
Under the Toxic Substances Control Act
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: As required under section 6(b)(1) of the Toxic Substances
Control Act (TSCA), EPA is issuing a final rule that establishes the
process and criteria that EPA will use to identify chemical substances
as either High-Priority Substances for risk evaluation, or Low-Priority
Substances for which risk evaluations are not warranted at the time.
The final rule describes the processes for formally initiating the
prioritization process on a selected candidate, providing opportunities
for public comment, screening the candidate against certain criteria,
and proposing and finalizing designations of priority. Prioritization
is the initial step in a new process of existing chemical substance
review and risk management activity established under TSCA.
DATES: This final rule is effective September 18, 2017.
ADDRESSES: The docket for this action, identified by docket
identification (ID) number EPA-HQ-OPPT-2016-0636, is available at
https://www.regulations.gov or at the Office of Pollution Prevention and
Toxics Docket (OPPT Docket) in the Environmental Protection Agency
Docket Center (EPA/DC), West William Jefferson Clinton Bldg., Rm. 3334,
1301 Constitution Ave. NW., Washington, DC 20460-0001. The Public
Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The telephone number for the Public
Reading Room is (202) 566-1744, and the telephone number for the OPPT
Docket is (202) 566-0280. Please review the visitor instructions and
additional information about the docket available at https://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
For technical information contact: Susanna W. Blair, Immediate
Office, Office of Pollution Prevention and Toxics, Environmental
Protection Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460-
0001; telephone number: (202) 564-4321; email address:
blair.susanna@epa.gov.
For general information contact: The TSCA-Hotline, ABVI-Goodwill,
422 South Clinton Ave., Rochester, NY 14620; telephone number: (202)
554-1404; email address: TSCA-Hotline@epa.gov.
SUPPLEMENTARY INFORMATION:
I. Executive Summary
A. What action is the Agency taking?
EPA is promulgating this final rule to establish the process and
criteria by which EPA will identify chemical substances as either High-
Priority Substances for risk evaluation, or Low-Priority Substances for
which risk evaluations are not warranted at the time.
B. Does this action apply to me?
This final rule does not establish any requirements on persons or
entities outside of the Agency. This action may, however, be of
interest to entities that are manufacturing or may manufacture or
import a chemical substance regulated under TSCA (e.g., entities
identified under North American Industrial Classification System
(NAICS) codes 325 and 324110). Since other entities may also be
interested, the Agency has not attempted to describe all the specific
entities and corresponding NAICS codes for entities that may be
interested in or affected by this action.
C. Why is the Agency taking this action?
This rulemaking is required by TSCA section 6(b)(1)(A), 15 U.S.C.
2605(b)(1)(A). Prioritization of chemical substances for further
evaluation will help to ensure that the Agency's limited resources are
conserved for those chemical substances most likely to present risks,
thereby furthering EPA's overall mission to protect health and the
environment.
D. What is the Agency's authority for taking this action?
This final rule is issued pursuant to the authority in TSCA section
6(b), 15 U.S.C. 2605(b).
E. What are the estimated incremental impacts of this action?
This final rule establishes the processes by which EPA intends to
designate chemical substances as either High or Low-Priority Substances
for risk evaluation. It does not establish any requirements on persons
or entities outside of the Agency. No incremental
[[Page 33754]]
impacts are therefore anticipated, and consequently EPA did not
estimate potential incremental impacts from this action.
II. Background
A. Statutory Requirements for Prioritization
TSCA section 6(b)(1), as amended by the Frank R. Lautenberg
Chemical Safety for the 21st Century Act (Pub. L. 114-182), requires
EPA to establish, by rule, a process for prioritizing chemical
substances for risk evaluation. Specifically, the law requires EPA to
establish ``a risk-based screening process, including criteria for
designating chemical substances as high-priority substances for risk
evaluations or low-priority substances for which risk evaluations are
not warranted at the time.'' 15 U.S.C. 2605(b)(1)(A). TSCA sections
6(b)(1) through (3) provide further specificity on both the process and
criteria, including preferences for certain chemical substances that
EPA must apply, procedural steps, definitions of High-Priority
Substances and Low-Priority Substances, and screening criteria that EPA
must consider in designating a chemical substance as either a High-
Priority Substance or a Low-Priority Substance. 15 U.S.C. 2605(b)(1)-
(3).
EPA published a proposed rule on January 17, 2017 setting forth the
draft process and criteria (Ref. 1). A detailed summary of the
statutory requirements for prioritization, EPA's methodology for
prioritizing existing chemicals for assessment under the TSCA Work Plan
before enactment of the TSCA amendments in 2016, and pre-proposal
stakeholder involvement activities and feedback was presented in the
proposed rule.
B. Interagency Collaboration
EPA is committed to engaging and collaborating with partner federal
agencies prior to and during the prioritization process. TSCA
specifically authorizes other federal agencies, at EPA's request, to:
(1) Make their services, personnel, and facilities available to the
Agency, (2) provide information, data, estimates, and statistics to the
Agency, and (3) grant EPA access to all information in its possession
as the Agency may reasonably determine to be necessary for the
administration of the Act. 15 U.S.C. 2625(a). EPA has a number of
existing mechanisms already in place to facilitate collaboration with
the Agency's federal partners and will continue to utilize them.
Collaboration with other federal agencies is an important step in
identifying chemicals for prioritization, evaluating risks from
chemicals, and during the risk management phase, if a chemical use is
determined to present an unreasonable risk.
EPA's collaboration with other federal agencies prior to and during
the risk-based prioritization process gives other agencies sufficient
time to work with the EPA in identifying any information about a
particular chemical substance that may be useful for formulating a
priority designation for that substance (e.g., conditions of use,
exposure scenarios, etc.). The Agency anticipates that it will at times
collaborate with the other statutory member agencies of the TSCA
Interagency Testing Committee (ITC), i.e., the Consumer Product Safety
Commission (CPSC), the Council on Environmental Quality (CEQ),
Department of Commerce, the Food and Drug Administration (FDA), the
National Cancer Institute (NCI), the National Institute of
Environmental Health Sciences (NIEHS), the National Institute for
Occupational Safety and Health (NIOSH), the National Science Foundation
(NSF); and the Occupational Safety and Health Administration (OSHA). 15
U.S.C. 2603(e)(2)(A). EPA also expects that such collaboration will
extend, when appropriate, to other federal agency partners not
specifically identified in TSCA as ITC members, such as the Agency for
Toxic Substances Disease Registry (ATSDR), the Department of Defense,
the National Aeronautics and Space Administration (NASA), and the
Office of Management and Budget (OMB). Finally, EPA anticipates that
its collaboration with other federal agencies may include, when
appropriate, the Small Business Administration's Office of Advocacy and
various other agencies to help facilitate outreach to the business
sector.
III. Overview of the Final Rule
This final rule incorporates all of the elements required by
statute, some additional criteria the Agency expects to consider,
clarifications for greater transparency, and additional procedural
steps to ensure effective implementation. In response to public
comments on the proposal, EPA is, among other things: (1) Deleting the
pre-prioritization provisions, and committing to further public comment
on how the Agency will identify candidates for prioritization, (2)
adding direct references in the final regulation to acknowledge the
Agency's commitment to implementing the best available science and
weight of the scientific evidence provisions in TSCA, and (3) adding a
number of provisions to clarify the limited meaning of a priority
designation, and committing the Agency to clear and effective
communication throughout the process.
EPA intends that the provisions of this rule be severable. In the
event that any individual provision or part of this rule is
invalidated, EPA intends that this would not render the entire rule
invalid, and that any individual provisions that can continue to
operate will be left in place.
IV. Detailed Discussion of Final Rule and Response to Comments
This unit provides a more in-depth discussion of the provisions in
the final rule, public comments received on the proposal, and revisions
made to the rule in response. A separate document that summarizes all
comments submitted on the proposal and EPA's responses to those
comments has been prepared and is available in the docket for this
rulemaking (Ref. 2).
A. Policy Objective
The final rule adopts the proposed codification of the policy
objective without revision. The prioritization process serves a
limited, but important, purpose in the new pipeline of existing
chemical review and management to help the Agency identify priorities
for further risk evaluation, to ensure that those priorities are
grounded in risk-based considerations (which may include, among other
considerations, the nature and extent of any existing regulation that
is intended to mitigate the hazards of a chemical substance), and to
provide the public and interested stakeholders with notice and an
opportunity to engage with the Agency and provide relevant information
prior to the start of the risk evaluation process on a particular
chemical. Through the process of prioritization, EPA is ultimately
making a judgment as to whether or not a particular chemical substance
warrants further assessment. As a general matter, the primary objective
of the process should be to guide the Agency towards identifying the
High-Priority Substances that have the greatest hazard and exposure
potential first. The prioritization process is not intended to be an
exact scoring or ranking exercise and, consistent with the proposed
rule, EPA is not adopting such a system in this rule. The precise order
(e.g., ranking or ordering chemicals based on their hazard and exposure
potential) in which EPA identifies High-Priority Substances (all of
which must meet the same statutory definition) should not be allowed to
[[Page 33755]]
slow the Agency's progress towards evaluating the risks from those
chemical substances. EPA intends to conserve its resources and the
Agency's deeper analytic efforts for the actual risk evaluation.
Low-Priority Substance designations serve the same policy
objectives. Chemical substances with low hazard and/or exposure
potential that meet the definition of Low-Priority Substances are taken
out of consideration for further assessment. This gives the public
notice of chemical substances for which the hazard and/or exposure
potential is anticipated to be low or nonexistent, and provides some
insight into which chemical substances are likely not to need
additional evaluation and risk management under TSCA. As a policy
matter, EPA is committed to making Low-Priority designations on an
ongoing basis beyond the statutory minimum.
B. Scope of Designations
Consistent with the proposed rule, EPA will designate the priority
of a ``chemical substance,'' as a whole, under this established
process, and will not limit its designation to a specific use or subset
of uses of a chemical substance. The statute is clear that EPA is to
designate the priority of the ``chemical substance''--not a condition
of use for a chemical substance. See, e.g., 15 U.S.C. 2605(b)(1)(A)
(``the Administrator shall establish, by rule, a risk-based screening
process, including criteria for designating chemical substances as
high-priority substances for risk evaluations'') (emphasis added);
2605(b)(1)(B) (definitions of high and low priority chemical
substances.)
Public comments on the proposed rule were split with respect to
this issue. Some commenters suggested that EPA should designate a
specific use of a chemical substance as High-Priority or a Low-
Priority. In general, these commenters argued that EPA should focus
only on chemical ``uses of greatest concern,'' in order to conserve EPA
resources, raising concern that EPA would be unable to meet its
statutory deadlines by focusing so broadly. These commenters argue that
nothing in the statute would foreclose this interpretation, and that
EPA's reading of the statute to require designation of ``chemical
substances'' as either High or Low-Priority is strained. One commenter
pointed to the ``sentinel exposure'' provision in the risk evaluation
context as evidence that Congress envisioned such a partial, use-based
approach.
EPA disagrees that the statutory text would support such an
interpretation for purposes of prioritization. The statute directs EPA
to make prioritization determinations on a ``chemical substance'' or
``substance,'' not on ``uses,'' see, e.g., 15 U.S.C. 2605(b)(1)(A)-(C),
and in most cases, without reference to ``the conditions of use.'' Had
Congress intended EPA to designate individual uses as high or low
priority, the statute would have used a different phrase or would have
otherwise clearly directed EPA to make determinations on high or low
priority ``uses.'' The clearest support for EPA's interpretation is
found in the statutory definitions of a High and Low Priority
Substance. Note, first, that these are definitions of high and low
priority ``substances.'' More critically, the definitions themselves
make clear that Congress intended EPA to prioritize the chemical as a
whole, rather than to prioritize particular uses or subsets of uses. A
High Priority substance is one that presents ``a potential hazard and a
potential route of exposure under the conditions of use;'' in other
words, the statute directs that the substance is High Priority based on
a potential risk from a single one of the chemical's various conditions
of use. Similarly, the statute directs that EPA can only designate a
substance as low priority if ``such substance does not meet the
standard . . . for designating a chemical substance a high-priority
substance.''
More generally, EPA believes the addition of the phrase ``the
conditions of use'' (emphasis added) was intended to move the Agency
away from its past practice of assessing only narrow uses of a chemical
substance, towards a more inclusive approach to chemical substance
management. Note that the phrase is plural, rather than singular
(conditions, not condition). While under the definition of ``conditions
of use,'' the Administrator retains some discretion to ``determine''
the conditions of use for each chemical substance, that discretion is
not unfettered. As EPA interprets the statute, the Agency is to
exercise that discretion consistent with the objective of determining
in a risk evaluation whether a chemical substance--not just individual
uses or other individual activities--presents an unreasonable risk. In
that regard, EPA will be guided by its best understanding, based on
legislative text and history, of the circumstances of manufacture,
processing, distribution in commerce, use and disposal Congress
intended EPA to consider in risk evaluations.
However, this does not mean that in prioritization, EPA will
necessarily consider every activity involving the chemical substance to
be a ``condition of use.'' TSCA defines a chemical's ``conditions of
use'' as ``the circumstances, as determined by the Administrator, under
which a chemical substance is intended, known, or reasonably foreseen
to be manufactured, processed, distributed in commerce, used, or
disposed of.'' 15 U.S.C. 2602(4). As discussed at greater length in the
final rule addressing procedures for chemical risk evaluation under
TSCA (RIN 2070-AK20), published elsewhere in this issue of Federal
Register, based on legislative history, statutory structure and other
evidence of Congressional intent, EPA has determined that certain
activities generally should not be considered to be ``conditions of
use.'' \1\ Thus early in the prioritization process, EPA will identify
the ``circumstances'' that constitute the ``conditions of use'' for
each chemical substance. A proposed determination would be presented
for public comment as part of the proposed designation of the substance
as High- or Low-Priority.
---------------------------------------------------------------------------
\1\ In the Risk Evaluation rule published elsewhere in this
issue of the Federal Register, EPA is adopting other revisions that
are applicable solely to the risk evaluation process, based on
statutory provisions that are exclusive to risk evaluations.
---------------------------------------------------------------------------
Accordingly, those activities that the Administrator determines
fall within the definition of ``conditions of use'' will be considered
during prioritization. When publishing proposed and final priority
designations pursuant to 40 CFR 702.9 and 40 CFR 702.11, the Agency
expects to identify the information, analysis and basis used to support
the designations, as well as the specific condition(s) of use that were
the basis for a High- or Low-Priority designation. A chemical substance
can only be designated as a Low-Priority if the ``conditions of use''
(as determined by the Administrator) do not meet the standard for High-
Priority designation.
C. Timeframe
TSCA section 6(b)(1)(C) requires that the prioritization process be
completed in no fewer than 9 months and no greater than 12 months.
Accordingly, the final rule specifies that the process--from initiation
to final designation--shall last between 9 and 12 months. EPA received
no significant comments on these timeframes, which are statutorily
mandated. However, some commenters requested that EPA clarify the
points of initiation and completion. Consistent with the proposal,
initiation of the prioritization process, for purposes of this
timeframe, begins upon publication of a notice in the Federal Register
that identifies a chemical substance for prioritization. Similarly, the
prioritization process is complete upon publication of a notice
[[Page 33756]]
in the Federal Register announcing a final priority designation. The
publication of a notice announcing a final designation of a chemical as
a High-Priority Substance simultaneously initiates a risk evaluation
pursuant to TSCA section 6(b)(4).
As indicated in the proposed rule, this timeframe serves dual
purposes. The minimum 9-month timeframe ensures that the general
public; potentially-affected industries; state, tribal, and local
governments; environmental and health non-governmental organizations;
and others have ample notice of upcoming federal action on a given
chemical substance, and opportunity to engage with EPA early in the
process. The 12-month maximum timeframe keeps the existing chemical
substances review pipeline in a forward motion, and prevents EPA from
getting mired in analysis before ever reaching the risk evaluation
step.
D. Categories of Chemical Substances
TSCA section 26 provides EPA with authority to take action on
categories of chemical substances. 15 U.S.C. 2625(c). ``Category of
Chemical Substances'' is defined at 15 U.S.C. 2625(c)(2)(A). EPA is
including in the final rule several provisions from the proposal with
respect to categories of chemical substances, without revision. EPA is
including, as proposed, a statement in the regulation that nothing in
the subpart shall be construed as a limitation on EPA's authority to
take action with respect to categories of chemical substances. Finally,
several commenters asked for clarification with respect to how EPA
might define a category of chemical substances. EPA is not adopting a
regulatory definition of a category, as the term is defined in TSCA at
15 U.S.C. 2625(c)(2)(A). However, should EPA determine to prioritize a
category of chemical substances, EPA would describe the basis for such
a determination in the Federal Register notice published to initiate
prioritization. As discussed elsewhere in this preamble, EPA has
revised the regulation at 40 CFR 702.7(b) to state that as part of the
initiation notice, EPA will provide an explanation of the rationale for
initiating the process on the chemical substance, thus ensuring the
public has notice and an opportunity to comment on any decision to
prioritize a category of chemical substances.
As defined in 15 U.S.C. 2625(c), a category of chemical substances
means a group of chemical substances the members of which are similar
in molecular structure, in physical, chemical or biological properties,
in use, or in mode of entrance into the human body or into the
environment, or the members of which are in some other way suitable for
classification as such for purposes of this Act, except that such term
does not mean a group of chemical substances which are grouped together
solely on the basis of their being new chemical substances.
EPA proposed to include a consideration of substitutes at the
candidate selection phase. This consideration was deleted from the
final rule for the reasons discussed in Unit IV(J).
E. Metals and Metal Compounds
A number of commenters expressed concern that EPA may choose not to
apply the March 2007 Framework for Metals Risk Assessment when
prioritizing metals or metal compounds. The commenters were concerned
that metals and metal compounds have unique attributes that are
different from organic and organometallic substances, which necessitate
special considerations when assessing their human health and ecological
risks. TSCA mandates use of the ``Framework for Metals Risk
Assessment'' to account for these attributes. Commenters' concerns stem
from a statement in EPA's proposed rule that it would consider
``relevant considerations'' from this document ``as appropriate'' when
prioritizing chemicals.
EPA fully recognizes the special attributes and behaviors of metals
and metal compounds, and the mandate to use the Framework document. EPA
did not intend the words ``as appropriate'' and ``relevant
considerations'' to suggest that EPA was seeking to avoid that mandate
or to otherwise diminish the significance of those considerations.
Accordingly, EPA revised the final rule to strike those words and
eliminate the confusion.
However, EPA notes that TSCA does not contemplate completion of a
full risk assessment during the prioritization phase. As the Metals
Framework is intended to guide EPA in conducting a risk assessment on a
metal or metal compound, the phrase ``as appropriate'' was merely
intended to reflect that no risk assessment would be conducted at this
phase, and thus certain sections of the Framework specific to
conducting risk assessments would not be relevant. In the context of
prioritization, EPA interprets the Metals Framework provision in TSCA
to require EPA to take into account the special attributes and
behaviors of metals and metal compounds as described in the Framework
document. For example, the document's Key Principles discuss the
differences between inorganic metals and organic and organometallic
compounds, and the unique attributes, properties, issues, and processes
associated with metals and metal compounds. Nevertheless, to avoid
confusion, EPA has deleted the phrase ``as appropriate'' from the
regulation.
F. Chemicals Subject to Prioritization
EPA is adopting these provisions from the proposal without
revision. Some commenters encouraged EPA to exclude certain groups of
chemicals from prioritization altogether, such as new chemicals
recently reviewed under TSCA section 5 and ``inactive'' chemicals.
Congress intended prioritization to be a public and transparent process
of determining which chemicals on the TSCA Inventory deserve further
evaluation. EPA does not believe TSCA allows EPA to simply exclude
chemical substances from this process. Chemical substances that do not
warrant risk evaluation would instead be proposed as Low-Priority
Substances, and the public given an opportunity to comment on that
determination through the procedures in this final rule.
With respect to chemical substances newly added to the TSCA
Inventory following EPA's completion of pre-manufacture review under
section 5 of TSCA (15 U.S.C. 2604), EPA expects that such chemical
substances are not likely to be selected as early High-Priority
candidates in light of the risk-related determination that the Agency
must make pursuant to TSCA section 5(a)(3). Chemicals that are
designated as ``inactive'' pursuant to the Active/Inactive Inventory
rule (RIN 2070-AK24) are still chemicals substances on the TSCA
Inventory, and therefore subject to prioritization. Nothing in TSCA
prohibits EPA from initiating the prioritization process on an
``inactive'' chemical substance and ultimately from designating the
priority of that chemical substance. However, similar to chemical
substances newly added to the TSCA Inventory, such chemicals may be
less likely to be selected as early High-Priority candidates. Whether
or not a chemical substance is actively manufactured would generally be
relevant to informing EPA's exposure judgments during the
prioritization process.
G. Section 26 Scientific Standards
The proposed rule explained that EPA did not need to specifically
reference or incorporate statutory requirements in the proposed rule in
order for them to have effect. A number of commenters opined on EPA's
lack of reference to the
[[Page 33757]]
new scientific standards in section 26 of TSCA. Some encouraged EPA to
broadly address how the new scientific terms apply to prioritization
decisions/process, and to acknowledge the role of section 26 in the
prioritization process. Commenters were split on whether and how EPA
should further define some of these terms.
As a matter of practice, EPA has been, and will continue to be,
committed to basing its decisions on the best available science and the
weight of the scientific evidence. In response to public comments on
the proposal, EPA has determined to make a number of additions to the
final rule to ensure that the science standards in TSCA are more
explicitly incorporated into the prioritization process. Specifically,
the final rule states that EPA's proposed priority designations under
40 CFR 702.9 and final priority designations under 40 CFR 702.11 will
be consistent with the scientific standards in 15 U.S.C. 2625(h) and
the weight of the scientific evidence in 15 U.S.C. 2625(i). These
changes clarify that EPA's proposed and final designations for both
High- and Low-Priority Substances will be consistent with TSCA's new
requirements in section 26 related to best available science and weight
of the scientific evidence.
H. Definitions
The final rule incorporates a number of key definitions. As in the
proposed rule, the final rule includes a definition of High-Priority
Substances and Low-Priority Substances. High-Priority Substance means a
chemical substance that EPA determines, without consideration of costs
or other non-risk factors, may present an unreasonable risk of injury
to health or the environment because of a potential hazard and a
potential route of exposure under the conditions of use, including an
unreasonable risk to potentially exposed or susceptible subpopulations
identified as relevant by EPA. A Low-Priority Substance means a
chemical substance that EPA concludes, based on information sufficient
to establish, without consideration of costs or other non-risk factors,
does not meet the standard for a High-Priority Substance.
EPA also incorporated the statutory definition of conditions of use
at 15 U.S.C. 2602(4). Conditions of use means the circumstances, as
determined by the Administrator, under which a chemical substance is
intended, known, or reasonably foreseen to be manufactured, processed,
distributed in commerce, used, or disposed of.
EPA further incorporated the statutory definition of potentially
exposed or susceptible subpopulation at 15 U.S.C. 2602(12). Potentially
exposed or susceptible subpopulation means a group of individuals
within the general population identified by the Administrator who, due
to either greater susceptibility or greater exposure, may be at greater
risk than the general population of adverse health effects from
exposure to a chemical substance or mixture, such as infants, children,
pregnant women, workers, or the elderly.
Finally, in response to comments that favored a definition of
``reasonably available information,'' EPA incorporated the definition
proposed in EPA's risk evaluation rule with some modifications to be
consistent with the definition in the final risk evaluation rule. In
the final rule, reasonably available information means information that
EPA possesses or can reasonably generate, obtain and synthesize for
use, considering the deadlines specified in TSCA section 6(b) for
prioritization and risk evaluation. Reasonably available information
includes information in EPA's possession that is confidential business
information under 15 U.S.C. 2613. Several commenters encouraged EPA to
take full advantage of its new information gathering authorities and
not limit the basis of its decisions to ``existing'' information. EPA
agrees that it makes sense to view information that can be obtained
through testing as ``reasonably available'' in some instances--
especially information that can be generated through short-term
testing, where it can be obtained within the relevant statutory
deadlines and the information would be of sufficient value to merit the
testing. Thus, the final rule modifies the definition of ``reasonably
available information'' to delete the word ``existing.'' Note that EPA
will, as appropriate, also require longer-term testing, and at times
will need to do so to more completely consider the hazard
characteristics and exposure pathways of a chemical substance. However,
EPA does not think information that could be generated through such
testing should be viewed as ``reasonably available''. Ultimately, EPA
will tailor its information gathering efforts. Further, the addition of
the reference to confidential business information was intended to
clarify that information in EPA's possession that is confidential
business information under 15 U.S.C. 2613 is also ``reasonably
available.''
I. Pre-Prioritization Considerations
EPA received a significant number of comments regarding the pre-
prioritization phase (Sec. 702.5 in the proposed rule) included in the
proposed rule. As EPA noted in the proposal, TSCA does not require EPA
to articulate in the prioritization rulemaking its expected activities
before prioritization, including those related to information gathering
or putting chemicals into some type of queue for input into the
prioritization pipeline. However, in an attempt to be more transparent
about these expected activities, EPA included in the proposal some
considerations for identifying both potential High- and Low-Priority
candidates, and general hazard and exposure considerations.
While commenters generally supported the concept and importance of
pre-prioritization activities, most took issue with the level of detail
and criteria in EPA's proposed rule and the expected lack of
transparency with respect to EPA's implementation, and most expressed a
strong desire to increase public participation and opportunities for
comment during the pre-prioritization phase. A number of commenters
stated that the Agency's proposed pre-prioritization process was
lacking sufficient detail, and that they were not able to provide
meaningful comment. In short, the details of implementing pre-
prioritization activities were the subject of widely differing, and
often irreconcilable views by commenters.
For these reasons, EPA does not believe it would be appropriate to
attempt to finalize a pre-prioritization process without further
discussions with interested stakeholders. As such, EPA has determined
to defer a final decision on the proposed pre-prioritization provisions
as part of this rule, and finalize at this time only the prioritization
process required under TSCA. The Agency will promptly initiate an
additional stakeholder process, to include an additional public comment
opportunity addressing EPA pre-prioritization activities. EPA is fully
committed to further dialogue on best practices for pre-prioritization
activities, and to carrying out these activities in a transparent,
science based manner, to ensure successful implementation of the
prioritization and risk evaluation processes.
Further, EPA appreciates the time commenters spent developing and
sharing their views on this particular subject. Commenters should rest
assured that these comments have been informative to the Agency and
will be considered as EPA continues to implement the recent amendments
to TSCA. EPA expects to re-engage the public on this matter as early as
Fall 2017, and these comments will serve as a solid foundation for
those discussions.
[[Page 33758]]
Following the additional stakeholder process, and in consideration
of public comments received, EPA will issue an appropriate final
action. While it is premature to determine the outcome of this future
process, it could foreseeably result in EPA formally establishing pre-
prioritization procedures in a final rule--either by first re-
proposing, or by finalizing based on the proposed rule. Alternatively,
for example, EPA may issue a guidance document that further describes
the pre-prioritization process. EPA will promptly evaluate public
comments received in response to the additional stakeholder process and
take the appropriate next steps. In the interim, the Agency fully
expects to move forward with prioritizing chemicals in accordance with
the procedures of the final rule. Indeed, TSCA compels the Agency to
proceed with designating a certain number of chemicals as High- or Low-
Priority by December of 2019. 15 U.S.C. 2605(b)(2)(B). Pre-
prioritization is not statutorily mandated, and, as a legal matter, not
a necessary precursor to the designation of High- and Low-Priority
substances. Pre-prioritization was intended to be a phase of expected
activities (e.g., potential candidate identification, information
gathering/review, etc.) to ensure a smooth process of moving chemicals
through the new pipeline of prioritization, risk evaluation, and (where
warranted) risk management. To illustrate, the Agency could, as a
general matter, draw potential candidates for prioritization from
existing Agency resources (including but not limited to, the 2014
update of the TSCA Work Plan for Chemical Assessments (Ref. 3) and the
Safer Chemicals Ingredients List (Ref. 4)). However, until EPA takes
final action on pre-prioritization as discussed above, the Agency will
not follow a formal process that identifies a chemical as being ``in
pre-prioritization.''
J. Information Availability
EPA expects to consider the existence and availability of risk-
related information on a candidate chemical substance before initiating
the prioritization process. EPA must complete its prioritization
process within 12 months once prioritization has been initiated for a
chemical substance, and then immediately initiate a risk evaluation for
a High-Priority Substance, and complete the risk evaluation within
three years of initiation. As a general practice, EPA intends to
resolve any concerns it may have about the sufficiency of information
about a given chemical substance for purposes of prioritization,
relative to the considerations in Sec. 702.9(a), before subjecting
that chemical substance to the prioritization process. Should EPA
identify a critical data need after the prioritization process has
already begun, it may be difficult or impossible for the Agency to
develop or acquire the necessary information, consistent with statutory
deadlines for prioritization. Although EPA will not establish or
implement a minimum information requirement of broader applicability,
the Agency anticipates that the types of information that are helpful
to inform and support prioritization decisions will become clearer as
the Agency gains experience with the prioritization process while also
allowing for advances in science and information gathering.
Commenters argued that EPA should not overuse its information
gathering authorities for a particular chemical before that chemical
has been identified as a High-Priority Substance for risk evaluation.
To avoid confusion, EPA has deleted several references to ensuring
sufficient information for purposes of risk evaluation at the
prioritization stage. While EPA has broad authorities to gather and
require generation of information, EPA did not intend to suggest that
it will routinely use its information gathering authorities for a
particular chemical without first evaluating the available information
to determine whether this is necessary. EPA expects to review and
consider the reasonably available existing hazard and exposure-related
information, and evaluate whether that information would be sufficient
to allow EPA to complete the prioritization process within the
statutory deadlines. To the extent the information is not currently
available or is insufficient, EPA will determine on a case-by-case
basis how to best proceed to ensure that information can be developed
and collected, reviewed and incorporated into analyses and decisions in
a timely manner.
To further clarify this intent, EPA has modified the final rule to
indicate that EPA generally expects to use a tiered approach to
information gathering. As a general matter, a tiered approach to data
gathering first involves a review of existing literature and available
information by EPA to determine data needs. EPA is also mindful of its
requirements with respect to the reduction of testing on vertebrate
animals under 15 U.S.C. 2603(h). For identified data needs, EPA may
issue a voluntary call to the public for relevant information or
otherwise engage directly with stakeholders, followed, as necessary, by
exercise of EPA's authorities under TSCA to require submission or
generation of new data.
K. Candidate Selection
TSCA requires that EPA give preference to chemical substances
listed in the 2014 update of the TSCA Work Plan for Chemical
Assessments that are persistent and bioaccumulative; known human
carcinogens; and/or highly toxic. TSCA section 6(b)(2)(B) further
requires that 50 percent of all ongoing risk evaluations be drawn from
the 2014 Update to the TSCA Work Plan for Chemical Assessments, meaning
that EPA will need to draw at least 50 percent of High-Priority
Substance candidates from the same list. By operation of this statutory
directive, all TSCA Work Plan chemical substances will eventually be
prioritized. These preferences are incorporated into the final rule
during candidate selection at 40 CFR 702.5(c), without revision from
the proposal. Aside from these statutory preferences, however, TSCA
does not specifically limit how EPA must ultimately select a chemical
substance to put into the prioritization process.
As described in the proposed rule, in practice, EPA expects to
select for High-Priority Substances those chemicals with the greatest
hazard and exposure potential first, consistent with the policy
objectives codified in 40 CFR 702.5(a). EPA has not revised the
regulatory text at 40 CFR 702.5(c) to include additional preferences.
The proposed rule included a statement that EPA is not required to
select candidates or initiate prioritization pursuant to 40 CFR 702.9
in any ranked or hierarchical order. EPA is striking this statement.
Some commenters encouraged EPA to adopt such a system and EPA is
retaining the discretion to do so by rule in the future. EPA does not
believe the statement in the proposed rule was necessary or had any
legal effect, since nothing in the rule or TSCA requires EPA to
implement an ordering or ranking system in selecting candidate chemical
substances for prioritization.
The proposed rule included a general objective for identifying
candidates for High-Priority Substances. In response to comments that
EPA more explicitly recognize Low-Priority designations as part of the
process, the final rule now includes a general objective for selecting
candidates for Low-Priority, consistent with the statutory definition
for Low-Priority Substances. As defined in TSCA, Low-Priority
Substances are those for which risk evaluation is not warranted at this
time. 15 U.S.C. 2605(b)(1)(A). As described in the final rule, EPA will
seek to identify
[[Page 33759]]
candidates for Low-Priority designation where the information on hazard
and exposure under the conditions of use for the chemical substance is
sufficient to establish that a risk evaluation is not warranted to
determine whether the chemical substance presents an unreasonable risk
of injury to health or the environment, including an unreasonable risk
to potentially exposed or susceptible subpopulations identified as
relevant by EPA.
EPA included in its proposed rule a general statement that EPA
``may consider the relative hazard and exposure of potential
candidate's substitutes'' in selecting a chemical for prioritization.
Some commenters believe strongly that EPA should not consider
substitutes as part of the prioritization phase because it is a
consideration more appropriate for the risk management phase. Others
had concern that considering the relative risk of substitutes had the
potential to lead to unlawful consideration of the availability of
substitutes at this phase--a non-risk factor the commenters assert is
expressly excluded from consideration during the prioritization
process. Several commenters expressed general support for consideration
of substitutes to the extent that it could help to avoid regrettable
substitution, and conserve both Agency and industry time and resources
that would result from inappropriate switches to other dangerous
chemicals. EPA has stricken the provision in question from the final
rule. EPA agrees that the consideration of alternatives is most
appropriately considered as part of any risk management rule.
L. Initiation of Prioritization
The prioritization process officially begins, for purposes of
triggering the 9 to 12-month statutory timeframe, when EPA publishes a
notice in the Federal Register identifying a chemical substance for
prioritization. The final rule includes a new provision clarifying that
EPA generally expects to provide an explanation in this notice for why
it chose to initiate the process for the particular chemical substance
(e.g., whether EPA views this as a potential candidate for High or Low
priority). This was in response to commenters' concerns that initiation
of the prioritization process could send strong signals to the public
regarding potential risks, even if certain uses of that chemical did
not prompt the initiation of prioritization. Note that a proposed
priority designation, as EPA clarified in the final rule, is not a
finding of unreasonable risk by the Agency.
Publication of the notice in the Federal Register also initiates a
90-day public comment period. For each chemical substance, EPA will
open a docket to facilitate receipt of public comments and access to
publicly available information throughout this process. Interested
persons are welcome and encouraged during this time to submit
information relevant to the chemical substance. Because TSCA
specifically requires the prioritization process to be risk-based and
EPA's determinations to exclude non-risk factors, relevant information
at this stage is limited to that which is risk-related.
Although the proposed rule specified that EPA would publish the
results of the screening review in this same notice, EPA's final rule
shifts the timing of the screening review, which will now occur after
the close of this initial 90-day public comment period. A number of
commenters expressed concern that the proposed rule did not guarantee
any opportunity for public comment prior to the screening review, and
many felt strongly that the Agency needed to engage the public to
inform prioritization decisions. The shift in timing puts the screening
review squarely within the prioritization process and affords the
public an opportunity to inform EPA's screening review before that
review. Thus, commenters are encouraged to submit relevant information
that may inform EPA's screening review. EPA will consider all relevant
information received during this comment period.
M. Screening Review
Following completion of the initial 90-day public comment period,
EPA will screen the selected candidate against the specific criteria
and considerations in TSCA section 6(b)(1)(A). Those criteria and
considerations are: (1) The chemical substance's hazard and exposure
potential; (2) the chemical substance's persistence and
bioaccumulation; (3) potentially exposed or susceptible subpopulations;
(4) storage of the chemical substance near significant sources of
drinking water; (5) the chemical substance's conditions of use or
significant changes in conditions of use; and (6) the chemical
substance's production volume or significant changes in production
volume. The Agency will develop guidance, consistent with OMB's Final
Bulletin for Agency Good Guidance Practices (72 FR 3432, January 25,
2007), to describe the implications of the criteria and considerations
and to explain how EPA generally expects to apply them during the
screening review step.
The final rule also includes an additional criterion, consistent
with the proposal: (7) Other risk-based criteria that EPA determines to
be relevant to the designation of the chemical substance's priority. As
explained in the proposal, this final criterion allows the screening
review to adapt with future changes in our understanding of science and
chemical risks. Should EPA rely on this criterion to support a proposed
designation, EPA would describe in the publication of proposed
designation the specific factors considered for such designation,
thereby affording the public notice and an opportunity to comment on
the basis for the proposed designation under this criterion. The
screening review is not a risk evaluation, but rather a review of
reasonably available information on the chemical substance that relates
to the screening criteria. EPA expects to review all sources of
relevant information, consistent with the scientific standards in 15
U.S.C. 2625(h), while conducting the screening review.
N. Proposed Designation
Based on the results of the screening review, EPA will propose to
designate the chemical substance as either a High-Priority Substance or
Low-Priority Substance, as those terms are defined in 40 CFR 702.3. In
making this proposed designation, as directed by the statute, EPA will
not consider costs or other non-risk factors.
The final rule provides that EPA will publish the proposed
designation in the Federal Register, along with an identification of
the information, analysis and basis used to support a proposed
designation. Pursuant to 15 U.S.C. 2625(j), EPA shall make this
information available to the public in the docket, subject to 15 U.S.C.
2613. Publication of this notice begins a second period of public
comment for 90 days, during which time the public may submit comments
on EPA's proposed designation. EPA will reopen the same docket opened
upon initiation of the prioritization process to facilitate receipt of
comments and information. Because the supporting documentation for a
proposed High-Priority Substance designation is likely to foreshadow
what will go into a scoping document for risk evaluation, EPA will be
particularly interested in comments on the accuracy of scope-related
information such as the chemical's ``conditions of use,'' at this step.
In the event of insufficient information at the proposed
designation
[[Page 33760]]
step, the proposed rule required EPA to propose to designate the
chemical as a High-Priority Substance. A number of commenters felt that
a ``default'' to High-Priority Substance would be an unfair result for
affected industries and/or irresponsible action by the Agency. This
provision has largely been stricken from the final rule, except for the
circumstance that is explicitly required in 15 U.S.C. 2505(b)(1), which
is now described in 40 CFR 702.9(e). TSCA requires that the
prioritization process lead to one of two outcomes by the end of the
12-month deadline: A High-Priority Substance designation or a Low-
Priority Substance designation. 15 U.S.C. 2605(b)(1)(B). On further
consideration, EPA believes the Agency is charged by the statute, and
will be able, to determine which of these priority categories each
chemical falls into during the prioritization process, and therefore it
is not necessary or appropriate to establish a default. EPA notes that
the statute specifically prohibits a default to Low-Priority, requiring
that a Low-Priority Substance designation be based on ``information
sufficient to establish'' that a chemical substance meets the
definition. 15 U.S.C. 2605(b)(1)(B)(ii). There is no comparable
statutory requirement for High-Priority Substance designations. 15
U.S.C. 2605(b)(1)(B)(i).
In response to a number of concerns raised by public commenters,
EPA is striking the ``issue preclusion'' provision related to proposed
designations as Low-Priority Substances, which stated that all comments
that could be raised on the issues in the proposed designation must be
presented during the comment period, or would be considered waived and
could not form the basis for an objection or challenge in any
subsequent administrative or judicial proceeding. Under general
principles of administrative law, commenters are required to identify
relevant available information and raise objections that could be
raised during established comment periods, and courts generally will
require commenters to have done so as a matter of exhaustion of
administrative remedies. EPA has concluded that these principles
provide sufficient assurance that commenters will raise timely
objections and provide timely information and has therefore decided to
strike the proposed regulatory text.
Although the final rule makes other clarifications to the
``Proposed Priority Designation'' provision, the standard for
designating High- and Low-Priority Substances has not changed from the
proposed rule. EPA will prioritize a ``chemical substance,'' and the
standard for a High-Priority Substance (``. . . may present an
unreasonable risk [. . .] because of a potential hazard and a potential
route of exposure . . .'') can be met by identification of one or more
condition of use that meet that standard. Conversely, in designating a
Low-Priority Substance (``. . . based on sufficient information, such
substance does not meet the standard for [. . .] a high-priority
substance . . .''), TSCA requires EPA to determine that under none of
the conditions of use, as determined by the Administrator, does the
chemical substance meet the definition of a High-Priority Substance.
O. Final Priority Designation
The last step in the prioritization process is for EPA to finalize
its designation of a chemical substance as either a High-Priority
Substance or a Low-Priority Substance. EPA will consider additional
relevant information received during the proposed designation step
before finalizing a priority designation, excluding any consideration
of costs or other non-risk factors. The final rule specifies that EPA
will publish a notice of the final priority designation in the Federal
Register, using the same docket that was used for the initiation and
proposal steps.
EPA has included additional regulatory text in the final rule,
clarifying that EPA would publish an identification of information,
analysis, and basis used to support the final designation, as required
under TSCA. Additionally, EPA amended the proposed rule to provide that
EPA generally expects to identify which condition(s) of use were the
primary bases for the priority designation. This was made in response
to some concerns that a priority designation for a chemical substance
could send strong signals to the public regarding potential risks.
P. Repopulation of High-Priority Substances
TSCA requires EPA to finalize a designation for at least one new
High-Priority Substance upon completion of a risk evaluation for
another chemical substance, other than a risk evaluation that was
requested by a manufacturer. Because the timing for the completion of
risk evaluation and/or the prioritization process will be difficult to
predict, EPA intends to satisfy this 1-off, 1-on replacement obligation
as follows: In the notice published in the Federal Register finalizing
the designation of a new High-Priority Substance, EPA generally expects
to identify the complete or near-complete risk evaluation that the new
High-Priority Substance will replace. So long as the designation occurs
within a reasonable time before or after the completion of the risk
evaluation, this will satisfy Congress' intent while avoiding
unnecessary delay and the logistical challenges that would be
associated with more perfectly aligning a High-Priority Substance
designation with the completion of a risk evaluation.
A few commenters suggested that EPA define a ``reasonable time''
for these purposes. Commenters expressed concern that, in the absence
of a defined period of time, a completed risk evaluation may never be
replaced with a new High-Priority Substance, slowing the pace of EPA's
overall progress towards reviewing the backlog of existing chemicals.
EPA has determined not to include a specific time frame in the
regulation that may be too prescriptive to implement. However, as a
general matter, EPA expects to designate a new High-Priority Substance
no later than 45 days following completion of a risk evaluation.
Q. Effect of Final Priority Designation
Final designation of a chemical substance as a High-Priority
Substance requires EPA to immediately begin a risk evaluation on that
chemical substance. Final designation of a chemical substance as a Low-
Priority Substance is a final agency action that means that a risk
evaluation of the chemical substance is not warranted at the time. This
does not preclude EPA from later revising the designation, if
warranted. EPA has added a provision in the final rule clarifying that
a final priority designation is neither a finding of unreasonable risk
to health or the environment, nor a finding of no unreasonable risk.
A Low-Priority Substance designation is explicitly subject to
judicial review. 15 U.S.C. 2618(a)(1)(C). A High-Priority Substance
designation is not a final agency action and is not subject to judicial
review. Rather, a High-Priority Substance designation prompts the
initiation of a risk evaluation. 15 U.S.C. 2605(b)(4). Upon the
conclusion of such a risk evaluation, EPA may determine that a chemical
substance does not present an unreasonable risk of injury to human
health or the environment under the conditions of use. Such a
determination must be issued in an order, and is a final agency action
subject to judicial review. 15 U.S.C. 2605(i). If EPA conversely
determines that a chemical substance presents an unreasonable risk of
injury to human health or the environment under the conditions of use,
that determination is not a final agency action and is not
[[Page 33761]]
subject to judicial review. TSCA mandates that the Agency must issue a
rule to apply certain requirements so that the chemical substance or
mixture no longer presents the unreasonable risk. 15 U.S.C. 2605(a).
Such a final rule is a final agency action and is subject to judicial
review.
R. Revision of Designation
TSCA provides that EPA may revise a final designation of a chemical
substance from a Low-Priority Substance to a High-Priority Substance at
any time based on information that is reasonably available to the
Agency. The final rule outlines the process the Agency will take to
revise such a designation. Essentially, the revision process involves
restarting the prioritization process, and applying the provisions in
the same way they would apply to a chemical that has not been
previously prioritized.
TSCA does not require a process for revising a High-Priority
Substance to a Low-Priority, and the final rule does not provide for
such revision. This is for good reason. Prioritization serves a limited
purpose: To identify chemicals for further evaluation. Once a chemical
has been identified as a High-Priority Substance, the risk evaluation
begins, the priority designation of the chemical having served its
purpose, and EPA is compelled to complete that risk evaluation within a
statutory 3-year deadline. Moreover, because the risk evaluation is
already underway at this point, EPA believes it would not make sense to
revisit whether or not a risk evaluation is warranted. EPA believes
Congress intended EPA to see the risk evaluation process through to its
conclusion and to make a finding under 15 U.S.C. 2605(i) that the
substance does not pose an unreasonable risk, not to revise a priority
designation.
S. Small Business Outreach
A few commenters recommended that EPA conduct targeted outreach to
small businesses early in the process of prioritization to identify
impacts to small businesses. Commenters suggest that the small business
community could benefit from background information on EPA's
activities, while EPA could receive valuable input from relevant small
businesses.
EPA welcomes the opportunity to engage with small businesses that
may use the subject chemical during the prioritization process,
particularly during the two 90-day public comment periods built into
the prioritization procedural rule, and will provide current
information about these activities through the Agency's Web site at
https://www.epa.gov/assessing-and-managing-chemicals-under-tsca. EPA
also expects to work closely with its federal partners at the Small
Business Administration, Office of Advocacy as a means to engage with
the small business community. TSCA mandates that both the
prioritization and risk evaluation processes be risk-based. As such,
EPA would be most interested in learning from small businesses and
other stakeholders about a particular chemical's uses, and potential
hazards and exposures. Economic impacts of any potential future
regulation have an important role during the consideration of risk
management measures, if and when warranted, but TSCA explicitly
excludes consideration of these impacts during prioritization and risk
evaluation actions.
V. References
The following is a listing of the documents that are specifically
referenced in this document. The docket includes these documents and
other information considered by EPA, including documents that are
referenced within the documents that are included in the docket, even
if the referenced document is not physically located in the docket. For
assistance in locating these other documents, please consult the
technical person listed under FOR FURTHER INFORMATION CONTACT.
1. EPA. Procedures for Prioritization of Chemicals for Risk
Evaluation Under the Toxic Substances Control Act; Proposed Rule.
Federal Register (82 FR 4825, January 17, 2017) (FRL-9957-74).
2. EPA. Procedures for Prioritization of Chemicals for Risk
Evaluation under TSCA: Response to Public Comments; SAN 5943; RIN
2070-AK23; EPA-HQ-OPPT-2016-0636. 2017.
3. EPA. TSCA Work Plan for Chemical Assessments: 2014 Update.
October 2014. Available online at: https://www.epa.gov/sites/production/files/2015-01/documents/tsca_work_plan_chemicals_2014_update-final.pdf.
4. EPA. Safer Chemical Ingredients List (SCIL). Available online at:
https://www.epa.gov/saferchoice/safer-ingredients. See also Master
Criteria, September 2012, Version 2.1, available online at: https://www.epa.gov/sites/production/files/2013-12/documents/dfe_master_criteria_safer_ingredients_v2_1.pdf.
VI. Statutory and Executive Order Reviews
Additional information about these statutes and Executive Orders
can be found at https://www2.epa.gov/laws-regulations/laws-and-executive-orders.
A. Executive Order 12866: Regulatory Planning and Review and Executive
Order 13563: Improving Regulation and Regulatory Review
This action is a significant regulatory action that was submitted
to the Office of Management and Budget (OMB) for review under Executive
Orders 12866 (58 FR 51735, October 4, 1993) and 13563 (76 FR 3821,
January 21, 2011). Any changes made in response to OMB recommendations
have been documented in the docket. This action is not subject to the
requirements of Executive Order 13771, entitled Reducing Regulation and
Controlling Regulatory Costs (82 FR 9339, February 3, 2017), because
this action does not impose any costs.
B. Paperwork Reduction Act (PRA)
This action does not contain any information collection activities
that require approval under the PRA, 44 U.S.C. 3501 et seq. This
rulemaking addresses internal EPA operations and procedures and does
not impose any requirements on the public.
C. Regulatory Flexibility Act (RFA)
I certify under section 605(b) of the RFA, 5 U.S.C. 601 et seq.,
that this action will not have a significant economic impact on a
substantial number of small entities. This rulemaking addresses
internal EPA operations and procedures and does not impose any
requirements on the public, including small entities.
D. Unfunded Mandates Reform Act (UMRA)
This action does not contain any unfunded mandate as described in
UMRA, 2 U.S.C. 1531-1538, and does not significantly or uniquely affect
small governments. The action imposes no enforceable duty on any state,
local or tribal governments or the private sector.
E. Executive Order 13132: Federalism
This action does not have federalism implications as specified in
Executive Order 13132 (64 FR 43255, August 10, 1999). It will not have
substantial direct effects on the states, on the relationship between
the national government and the states, or on the distribution of power
and responsibilities among the various levels of government.
F. Executive Order 13175: Consultation and Coordination With Indian
Tribal Governments
This action does not have tribal implications as specified in
Executive Order 13175 (65 FR 67249, November 9, 2000). It will not have
substantial direct effects on one or more Indian tribes, on
[[Page 33762]]
the relationship between the Federal Government and Indian tribes, or
on the distribution of power and responsibilities between the Federal
Government and Indian tribes. Thus, Executive Order 13175 does not
apply to this action.
G. Executive Order 13045: Protection of Children From Environmental
Health Risks and Safety Risks
EPA interprets Executive Order 13045 (62 FR 19885, April 23, 1997)
as applying only to those regulatory actions that concern environmental
health or safety risks that the EPA has reason to believe may
disproportionately affect children, per the definition of ``covered
regulatory action'' in section 2-202 of the Executive Order. This
action is not subject to Executive Order 13045 because it does not
concern an environmental health risk or safety risk.
H. Executive Order 13211: Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution, or Use
This action is not a ``significant energy action'' as defined in
Executive Order 13211 (66 FR 28355, May 22, 2001), because it is not
likely to have a significant adverse effect on the supply, distribution
or use of energy. This rulemaking addresses internal EPA operations and
procedures and does not impose any requirements on the public.
I. National Technology Transfer and Advancement Act (NTTAA)
This rulemaking does not involve any technical standards, and is
therefore not subject to considerations under NTTAA section 12(d), 15
U.S.C. 272 note.
J. Executive Order 12898: Federal Actions To Address Environmental
Justice in Minority Populations and Low-Income Populations
This action does not establish an environmental health or safety
standard, and is therefore not is not subject to environmental justice
considerations under Executive Order 12898 (59 FR 7629, February 16,
1994). This rulemaking addresses internal EPA operations and procedures
and does not have any impact on human health or the environment.
VII. Congressional Review Act (CRA)
This rule is exempt from the CRA, 5 U.S.C. 801 et seq., because it
is a rule of agency organization, procedure or practice that does not
substantially affect the rights or obligations of non-agency parties.
List of Subjects in 40 CFR Part 702
Environmental protection, Chemical substances, Chemicals, Hazardous
substances, Health and safety, Prioritization, Screening, Toxic
substances.
Dated: June 22, 2017.
E. Scott Pruitt,
Administrator.
Therefore, 40 CFR chapter I, subchapter R, is amended as follows:
PART 702--GENERAL PRACTICES AND PROCEDURES
0
1. The authority citation for part 702 is revised to read as follows:
Authority: 15 U.S.C. 2605 and 2619.
0
2. Add subpart A to read as follows:
Subpart A--Procedures for Prioritization of Chemical Substances for
Risk Evaluation
Sec.
702.1 General provisions.
702.3 Definitions.
702.4 [Reserved]
702.5 Candidate selection.
702.7 Initiation of prioritization process.
702.9 Screening review and proposed priority designation.
702.11 Final priority designation.
702.13 Revision of designation.
702.15 Effect of designation as a low-priority substance.
702.17 Effect of designation as a high-priority substance.
Subpart A--Procedures for Prioritization of Chemical Substances for
Risk Evaluation
Sec. 702.1 General provisions.
(a) Purpose. This regulation establishes the risk-based screening
process for designating chemical substances as a High-Priority
Substance or a Low-Priority Substance for risk evaluation as required
under section 6(b) of the Toxic Substances Control Act, as amended (15
U.S.C. 2605(b)).
(b) Scope of designations. EPA will make priority designations
pursuant to these procedures for a chemical substance, not for a
specific condition or conditions of uses of a chemical substance.
(c) Categories of chemical substances. Nothing in this subpart
shall be interpreted as a limitation on EPA's authority under 15 U.S.C.
2625(c) to take action, including the actions contemplated in this
subpart, on a category of chemical substances.
(d) Prioritization timeframe. The Agency will publish a final
priority designation for a chemical substance in no fewer than 9 months
and no longer than 1 year following initiation of prioritization
pursuant to Sec. 702.7.
(e) Metals or metal compounds. EPA will identify priorities for
chemical substances that are metals or metal compounds in accordance
with 15 U.S.C. 2605(b)(2)(E).
(f) Applicability. These regulations do not apply to any chemical
substance for which a manufacturer requests a risk evaluation under 15
U.S.C. 2605(b)(4)(C).
(g) Scientific standards and weight of the scientific evidence.
EPA's proposed priority designations under Sec. 702.9 and final
priority designations under Sec. 702.11 will be consistent with the
scientific standards provision in 15 U.S.C. 2625(h) and the weight of
the scientific evidence provision in 15 U.S.C. 2625(i).
(h) Interagency collaboration. EPA will consult with other relevant
Federal Agencies during the administration of this subpart.
Sec. 702.3 Definitions.
For purposes of this subpart, the following definitions apply:
Act means the Toxic Substances Control Act, as amended (15 U.S.C.
2601 et seq.).
Conditions of use means the circumstances, as determined by the
Administrator, under which a chemical substance is intended, known, or
reasonably foreseen to be manufactured, processed, distributed in
commerce, used, or disposed of.
EPA means the U.S. Environmental Protection Agency.
High-priority substance means a chemical substance that EPA
determines, without consideration of costs or other non-risk factors,
may present an unreasonable risk of injury to health or the environment
because of a potential hazard and a potential route of exposure under
the conditions of use, including an unreasonable risk to potentially
exposed or susceptible subpopulations identified as relevant by EPA.
Low-priority substance means a chemical substance that EPA
concludes, based on information sufficient to establish, without
consideration of costs or other non-risk factors, does not meet the
standard for a High-Priority Substance.
Potentially exposed or susceptible subpopulation means a group of
individuals within the general population identified by the
Administrator who, due to either greater susceptibility or greater
exposure, may be at greater risk than the general population of adverse
health effects from exposure to a chemical substance or mixture, such
as infants, children,
[[Page 33763]]
pregnant women, workers, or the elderly.
Reasonably available information means information that EPA
possesses or can reasonably generate, obtain and synthesize for use,
considering the deadlines specified in 15 U.S.C. 2605(b) for
prioritization and risk evaluation. Information that meets such terms
is reasonably available information whether or not the information is
confidential business information that is protected from public
disclosure under 15 U.S.C. 2613.
Sec. 702.4 [Reserved]
Sec. 702.5 Candidate selection.
(a) General objective. In selecting candidates for a High-Priority
Substance designation, it is EPA's general objective to select those
chemical substances with the greatest hazard and exposure potential
first, considering reasonably available information on the relative
hazard and exposure of potential candidates. In selecting candidates
for Low-Priority Substance designation, it is EPA's general objective
to select those chemical substances with hazard and/or exposure
characteristics under the conditions of use such that a risk evaluation
is not warranted at the time to determine whether the chemical
substance presents an unreasonable risk of injury to health or the
environment, including an unreasonable risk to potentially exposed or
susceptible subpopulations identified as relevant by EPA.
(b) Available information. EPA expects to ensure that there is
reasonably available information to meet the deadlines for
prioritization under the Act.
(c) Preferences and TSCA work plan. In selecting a candidate for
prioritization as a High-Priority Substance, EPA will:
(1) Give preference to:
(i) Chemical substances that are listed in the 2014 update of the
TSCA Work Plan for Chemical Assessments as having a persistence and
bioaccumulation score of 3; and
(ii) Chemical substances that are listed in the 2014 update of the
TSCA Work Plan for Chemical Assessments that are known human
carcinogens and have high acute and chronic toxicity; and
(2) Identify a sufficient number of candidates from the 2014 update
of the TSCA Work Plan for Chemical Assessments to ensure that, at any
given time, at least 50 percent of risk evaluations being conducted by
EPA are drawn from that list until all substances on the list have been
designated as either a High-Priority Substance or Low-Priority
Substance pursuant to Sec. 702.11.
(d) Purpose. The purpose of the preferences and criteria in
paragraphs (a) through (c) of this section is to inform EPA's decision
whether or not to initiate the prioritization process pursuant to Sec.
702.7, and the proposed designation of the chemical substance as either
a High-Priority Substance or a Low-Priority Substance pursuant to Sec.
702.9.
(e) Insufficient information. If EPA believes it would not have
sufficient information for purposes of prioritization, EPA generally
expects to obtain the information necessary to inform prioritization
prior to initiating the process pursuant to Sec. 702.9, using
voluntary means of information gathering and, as necessary, exercising
its authorities under the Act in accordance with the requirements of 15
U.S.C. 2603, 15 U.S.C. 2607, and 15 U.S.C. 2610. In exercising its
authority under 15 U.S.C. 2603(a)(2), EPA will identify the need for
the information in accordance with 15 U.S.C. 2603(a)(3).
Sec. 702.7 Initiation of prioritization process.
(a) EPA generally expects to initiate the prioritization process
for a chemical substance only when it believes that the information
necessary to prioritize the substance is reasonably available.
(b) EPA will initiate prioritization by publishing a notice in the
Federal Register identifying a chemical substance for prioritization.
EPA will include a general explanation in this notice for why it chose
to initiate the process on the chemical substance.
(c) The prioritization timeframe in Sec. 702.1(d) begins upon
EPA's publication of the notice described in paragraph (b) of this
section.
(d) Publication of the notice in the Federal Register pursuant to
paragraph (b) of this section will initiate a period of 90 days during
which interested persons may submit relevant information on that
chemical substance. Relevant information might include, but is not
limited to, any information that may inform the screening review
conducted pursuant to Sec. 702.9(a). EPA will open a separate docket
for each chemical substance to facilitate receipt of information.
(e) EPA may, in its discretion, extend the public comment period in
paragraph (d) of this section for up to three months in order to
receive or evaluate information submitted under 15 U.S.C.
2603(a)(2)(B). The length of the extension will be based upon EPA's
assessment of the time necessary for EPA to receive and/or evaluate
information submitted under 15 U.S.C. 2603(a)(2)(B).
Sec. 702.9 Screening review and proposed priority designation.
(a) Screening review. Following the close of the comment period
described in Sec. 702.7(d), including any extension pursuant to
paragraph (e) of that section, EPA will generally use reasonably
available information to screen the candidate chemical substance
against the following criteria and considerations:
(1) The chemical substance's hazard and exposure potential;
(2) The chemical substance's persistence and bioaccumulation;
(3) Potentially exposed or susceptible subpopulations;
(4) Storage of the chemical substance near significant sources of
drinking water;
(5) The chemical substance's conditions of use or significant
changes in conditions of use;
(6) The chemical substance's production volume or significant
changes in production volume; and
(7) Other risk-based criteria that EPA determines to be relevant to
the designation of the chemical substance's priority.
(b) Information sources. In conducting the screening review in
paragraph (a) of this section, EPA expects to consider sources of
information relevant to the listed criteria and consistent with the
scientific standards provision in 15 U.S.C. 2625(h), including, as
appropriate, sources for hazard and exposure data listed in Appendices
A and B of the TSCA Work Plan Chemicals: Methods Document (February
2012).
(c) Proposed designation. Based on the results of the screening
review in paragraph (a) of this section, relevant information received
from the public as described in Sec. 702.7(d), and other information
as appropriate and consistent with 15 U.S.C. 2625(h) and (i), EPA will
propose to designate the chemical substance as either a High-Priority
Substance or Low-Priority Substance, along with an identification of
the information, analysis, and basis used to support the proposed
designation.
(d) Costs and non-risk factors. EPA will not consider costs or
other non-risk factors in making a proposed priority designation.
(e) Insufficient information. If information remains insufficient
to enable the proposed designation of the chemical substance as a Low-
Priority Substance after any extension of the initial public comment
period pursuant
[[Page 33764]]
to Sec. 702.7(e), EPA will propose to designate the chemical substance
as a High-Priority Substance.
(f) Conditions of use. EPA will propose to designate a chemical
substance as a High-Priority Substance based on the proposed conclusion
that the chemical substance satisfies the definition of High-Priority
Substance in Sec. 702.3 under one or more activities that the Agency
determines constitute conditions of use. EPA will propose to designate
a chemical substance as a Low-Priority Substance based on the proposed
conclusion that the chemical substance meets the definition of Low-
Priority Substance in Sec. 702.3 under the activities that the Agency
determines constitute conditions of use.
(g) Publication. EPA will publish the proposed designation in the
Federal Register, along with an identification of the information,
analysis and basis used to support a proposed designation, in a form
and manner that EPA deems appropriate, and provide a comment period of
90 days, during which time the public may submit comment on EPA's
proposed designation. EPA will open a docket to facilitate receipt of
public comment.
Sec. 702.11 Final priority designation.
(a) After considering any additional information collected from the
proposed designation process in Sec. 702.9, as appropriate, EPA will
finalize its designation of a chemical substance as either a High-
Priority Substance or a Low-Priority Substance consistent with 15
U.S.C. 2625(h) and (i).
(b) EPA will not consider costs or other non-risk factors in making
a final priority designation.
(c) EPA will publish each final priority designation in the Federal
Register, along with an identification of the information, analysis,
and basis used to support a final designation consistent with 15 U.S.C.
2625(h), (i) and (j). For High-Priority Substance designations, EPA
generally expects to indicate which condition(s) of use were the
primary basis for such designations.
(d) As required in 15 U.S.C. 2605(b)(3)(C), EPA will finalize a
designation for at least one High-Priority Substance for each risk
evaluation it completes, other than a risk evaluation that was
requested by a manufacturer pursuant to subpart B of this part. The
obligation in 15 U.S.C. 2605(b)(3)(C) will be satisfied by the
designation of at least one High-Priority Substance where such
designation specifies the risk evaluation that the designation
corresponds to, and where the designation occurs within a reasonable
time before or after the completion of the risk evaluation.
Sec. 702.13 Revision of designation.
EPA may revise a final designation of a chemical substance from
Low-Priority to High-Priority Substance at any time based on reasonably
available information. To revise such a designation, EPA will re-
initiate the prioritization process on that chemical substance in
accordance with Sec. 702.7, re-screen the chemical substance and
propose a priority designation pursuant to Sec. 702.9, and finalize
the priority designation pursuant to Sec. 702.11.
Sec. 702.15 Effect of designation as a low-priority substance.
Designation of a chemical substance as a Low-Priority Substance
under Sec. 702.11 means that a risk evaluation of the chemical
substance is not warranted at the time, but does not preclude EPA from
later revising the designation pursuant to Sec. 702.13, if warranted.
Designation as a Low-Priority Substance is not a finding that the
chemical substance does not present an unreasonable risk, but rather
that it does not meet the High-Priority Substance definition.
Sec. 702.17 Effect of designation as a high-priority substance.
Final designation of a chemical substance as a High-Priority
Substance under Sec. 702.11 initiates a risk evaluation pursuant to
subpart B of this part. Designation as a High-Priority Substance is not
a final agency action and is not subject to judicial review until the
date of promulgation of the associated final rule under section 6(a).
Designation as a High-Priority Substance is not a finding that the
chemical substance presents an unreasonable risk.
[FR Doc. 2017-14325 Filed 7-19-17; 8:45 am]
BILLING CODE 6560-50-P