109th CONGRESS
1st Session
S. 1391
To amend the Toxic Substances Control Act to reduce the exposure
of children, workers, and consumers to toxic chemical substances.
IN THE SENATE OF THE UNITED STATES
July 13, 2005
Mr. LAUTENBERG (for himself, Mr. JEFFORDS, Mrs. BOXER, Mr. KERRY, Mr. CORZINE,
Mrs. CLINTON, and Mr. KENNEDY) introduced the following bill; which was read
twice and referred to the Committee on Environment and Public Works
A BILL
To amend the Toxic Substances Control Act to reduce the exposure
of children, workers, and consumers to toxic chemical substances.
Be it enacted by the Senate and House of Representatives of the United
States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the `Child, Worker, and Consumer-Safe Chemicals Act
of 2005' or as the `Kid Safe Chemicals Act'.
SEC. 2. FINDINGS, POLICIES, AND GOALS.
(a) Findings- Congress finds the following:
(1) The incidence of some diseases and disorders which have been linked
to chemical exposures are on the rise.
(2) The metabolism, physiology, and exposure patterns of developing fetuses,
infants, and children to toxic chemicals differ from those of adults, which
makes children more vulnerable than adults to the harmful effects of exposure
to some synthetic chemicals.
(3) Unlike pharmaceuticals and pesticides, manufacturers of most chemical
substances are not required under current law to supply human or environmental
toxicity information before selling their products to the public. Consequently,
the vast majority of chemicals used in commercial products have never had
any Federal review to evaluate potential toxicity to infants, children,
developing fetuses, or adults.
(4) Biomonitoring tests have shown that a fetus, infant, or child in the
United States today often have many synthetic chemicals in their blood and
tissue.
(5) Despite these alarming discoveries, the Environmental Protection Agency
has reviewed the human health risks of only an estimated 2 percent of the
62,000 chemicals that were in use in 1976, when Congress passed the Toxic
Substances Control Act (15 U.S.C. 2601 et seq.). The Environmental Protection
Agency has issued regulations to ban or restrict the use of only 5 chemical
substances in 29 years, due to the law's excessively high administrative
and legal hurdles.
(6) A fundamental overhaul of United States chemical management is needed
to build a non-toxic environment for our children.
(b) Policy- It is the policy of the United States to--
(1) promote children's health as a paramount national goal, recognizing
that developing fetuses, infants, and children are uniquely vulnerable to
the harmful effects of some toxic chemicals during all stages of their development;
(2) minimize toxic substances in the environment of children, workers, and
consumers by--
(A) promoting the use of safer substitutes and solutions to reduce exposure
to hazardous chemicals by rewarding business innovation;
(B) holding chemical manufacturers responsible for providing complete
health and safety data for each chemical they produce prior to distribution
of that chemical substance in commerce; and
(C) providing the Environmental Protection Agency with authority to allow
the commercial distribution of chemical substances only where the data
and information show there is a reasonable certainty that the chemical
substances pose no harm to human health or the environment; and
(3) provide the public and workers the full right to know about the health
effects of the chemical substances to which they are exposed.
(c) Goals- It is the goal of the United States to eliminate the exposure of
all children, workers, consumers, and sensitive subgroups to harmful chemicals
distributed in commerce by 2020 by--
(1) identifying the highest priority chemical substances for review by 2007;
(2) making a safety determination for, at a minimum, the first 300 priority
chemical substances by 2010 and banning or restricting the use of a chemical
substance if it cannot be shown to meet the safety standard; and
(3) making a safety determination for all chemical substances by 2020, and
banning or restricting the use of a chemical if it cannot be shown to meet
the safety standard.
SEC. 3. PROTECTION OF CHILDREN'S HEALTH FROM CHEMICAL SUBSTANCES.
(a) In General- The Toxic Substances Control Act (15 U.S.C. 2601 et seq.)
is amended by adding at the end the following:
`TITLE V--CHILD SAFE CHEMICALS
`SEC. 501. MANUFACTURER SAFETY CERTIFICATIONS.
`(a) Safety Statement and Information- Not later than 1 year after the date
of enactment of this title, each manufacturer of a chemical substance distributed
in commerce shall submit to the Administrator--
`(1) a statement signed by the chief executive officer of the manufacturer
certifying, based on available information after a good faith inquiry, that--
`(A) the chemical substance meets the safety standard defined in section
503(a); or
`(B) there is insufficient data to determine whether the chemical substance
meets that safety standard; and
`(2) all reasonably available information in the company's possession or
control that has not previously been submitted to the Administrator regarding
the physical, chemical, and toxicological properties of the chemical substance,
and the annual production volume and known uses of, and exposure and fate
information relating to, the chemical substance.
`(b) Updating of Information- Each manufacturer of a chemical substance described
in subsection (a) shall update the information described in subsection (a)(2)--
`(1) at a minimum, every 3 years; and
`(2) at any time at which there becomes available significant new information
regarding a physical, chemical, or toxicological property of, or exposure
to, the chemical substance, including at a minimum any information that
shows a new potential toxic effect, corroborates previous information showing
or suggesting a toxic effect, or suggests a toxic effect at a lower dose
than previously demonstrated.
`(c) New Chemical Substances- Prior to a new chemical substance being distributed
in commerce, the chief executive officer of the manufacturer must certify
the safety of that chemical substance as directed in subsection (a).
`(d) Definition of Toxicological Property- For the purposes of this title,
`toxicological property' means actual or potential toxicity, bioconcentration,
or other biological or adverse effects, including but not limited to effects
on mortality, morbidity, reproduction, development, the immune system, the
endocrine system, the brain or nervous system, or any other biological functions
in humans or animals.
`SEC. 502. PRIORITY LIST OF CHEMICAL SUBSTANCES FOR EPA SAFETY DETERMINATION.
`(1) IN GENERAL- Not later than 18 months after the date of enactment of
this title, the Administrator shall develop a priority list of not less
than 300 chemical substances (referred to in this title as the `priority
list') which shall be the first chemical substances for which a safety determination
is made, as set forth in section 503. Chemical substances that may pose
the greatest risk to humans shall be ranked as highest priority.
`(2) UPDATING OF LIST- Additional chemical substances shall be added to
the priority list at least annually until all chemical substances which
meet the criteria set forth in subsection (b) have been added to the priority
list.
`(3) TREATMENT AS FINAL AGENCY ACTION- Development of the priority list
shall not be considered to be a final agency action for the purpose of subchapter
II of chapter 5, and chapter 7, of title 5, United States Code (commonly
known as `the Administrative Procedure Act'), but the Administrator's failure
to issue or update a priority list by the deadline established in the Act
shall be considered a failure to perform a nondiscretionary duty.
`(b) Criteria for Identifying Prioritized Chemical Substances- In determining
the priority list of chemical substances for a safety determination, the Administration
shall take into account whether the chemical substance--
`(1) is found in human blood, fluids, or tissue, unless the chemical substance
is not synthetic and is naturally present at the level found in blood, fluids,
or tissue;
`(2) is found in food or drinking water, unless the chemical substance is
not synthetic and is naturally present at the level found in food or drinking
water;
`(3) is manufactured or discharged into the environment at a volume of more
than 1,000,000 pounds annually;
`(4) is a known or suspected reproductive, neurological, or immunological
toxicant, carcinogen, mutagen, or endocrine disruptor, or causes negative
developmental effects; or
`(5) is persistent or bioaccumulative.
`SEC. 503. EPA SAFETY DETERMINATION FOR CHEMICAL SUBSTANCES.
`(a) Definition of Safety Standard- In this section, the term `safety standard'
means, with respect to a chemical substance (or another chemical substance
with a common mechanism of action)--
`(1) a standard that provides a reasonable certainty that no harm will be
caused by aggregate exposure of a fetus, infant, child, worker, or member
of other sensitive subgroup; and
`(2) in the case of a fetus, infant, or child, a standard that accounts
for their special vulnerability to potential pre- and post-natal exposures
by applying an additional 10 fold safety factor to the level established
for adults.
`(b) Chemical Safety Information-
`(1) IN GENERAL- On receipt of a request from the Administrator, a manufacturer
of the chemical substance shall provide to the Administrator all information
requested under this subsection.
`(2) INFORMATION- In making a determination with respect to a chemical substance
under subsection (c), the Administrator shall take into account each of
the following:
`(A) Environmental fate and transport, including degradation, persistence
in the environment, mobility, and distribution across environmental media,
of the chemical substance.
`(B) Biological fate and transport, including metabolism, bioaccumulation
and biomagnification potential, and toxicokinetics.
`(C) Acute, subchronic, and chronic human health effects of exposure to
the substance, including reproductive, developmental, genotoxic, neurotoxic,
immunotoxic, and endocrine-disrupting effects.
`(D) The potential for additive or synergistic effects to result from
exposure to multiple chemical substances.
`(E) The ecotoxicity of a chemical substance to avian, terrestrial, and
aquatic species.
`(F) The presence of the chemical substance in, at a minimum--
`(i) human blood, fluids, or tissue; and
`(ii) food or drinking water.
`(G) The uses of the chemical substance and associated known and potential
releases and exposures.
`(3) MINIMUM DATA SET- The Administrator shall establish a minimum set of
data requirements that would ensure that determinations under subsection
(c) are based on reliable data.
`(4) TIERING PROCESS- The Administrator shall have the authority to develop
a tiering process for the submission of the information.
`(c) Safety Determination-
`(A) IN GENERAL- Not later than 3 years after the date on which a chemical
substance has been placed on the priority list, the Administrator shall
determine whether the manufacturer has established that the chemical substance
meets the safety standard.
`(i) NOTICE OF PENDING DETERMINATION- If the Administrator fails to
act within the deadlines established in subparagraph (A), a manufacturer
affected by the failure to act shall issue to the Administrator, the
public, and each known customer of a chemical substance a written notice
that a determination of safety is pending.
`(ii) FAILURE OF ADMINISTRATOR TO ACT- Not later than 5 years after
the date on which a chemical substance has been placed on the priority
list, if the Administrator has not made a determination under subparagraph
(A), the chemical substance shall not be distributed in commerce.
`(2) OTHER CHEMICAL SUBSTANCES- Not later than 15 years after the date of
enactment of this title, the Administrator shall determine whether each
chemical substance distributed in commerce meets the safety standard. Not
less than 1 time every 15 years thereafter, the Administrator shall reassess
the safety of all chemical substances distributed in commerce.
`(3) NEW CHEMICAL SUBSTANCES- As of the date that is 90 days after the date
of enactment of this title, no new chemical substance shall be distributed
in commerce unless the chemical substance has met the safety standard under
subsection (a), as determined by the Administrator.
`(1) IN GENERAL- Within 5 years after the date of enactment of this title,
and every 3 years thereafter, a manufacturer of a chemical substance shall
carry out a biomonitoring study to determine the presence in human blood,
fluids, or tissue for any chemical substance--
`(A) which is manufactured in quantities greater than 1,000,000 pounds
during 1 calendar year; or
`(B) for any chemical substance distributed in commerce--
`(i) to which humans are exposed; and
`(ii) for which there is cause for concern regarding the exposure (as
determined by the Administrator), such as a potential for persistence
or bioaccumulation of the chemical substance.
`(2) STANDARD- The Administrator shall by regulation establish a standard
for biomonitoring studies under this subsection that includes--
`(A) the use of a representative sample that ensures that likely exposed
populations including children are oversampled; and
`(B) a determination of appropriate detection levels of chemical substances.
`(3) SUBSTANCE DETECTION- A manufacturer of a chemical substance subject
to paragraph (1) shall make available to the public a practicable method
(as determined by the Administrator) for detecting the presence of the substance
or any of its metabolites in human blood, fluids, and tissue.
`SEC. 504. REDUCTION OF HEALTH HAZARDS FOR CHILDREN, WORKERS, AND CONSUMERS.
`(a) Market Restrictions- No person shall manufacture a chemical substance
if--
`(1) the Administrator determines that the person failed to act in accordance
with section 501 or section 503;
`(2) the Administrator determines that the chemical substance does not meet
the safety standard defined in section 503(a); or
`(3) the Administrator has not made a safety determination for the chemical
substance by the deadline established in paragraph (1)(B)(ii), (2), or (3)
of section 503(c).
`(b) Use Exemptions- The Administrator may allow manufacturing for a specified
use of any chemical substance where the Administrator determines such use
meets the safety standard defined in section 503(a).
`(c) Exemption From Biomonitoring- Any manufacturer that submitted to the
Administrator a biomonitoring study of a chemical substance on or before the
date of enactment of this title shall be exempt from the initial biomonitoring
under section 503(d) for that chemical substance.
`(1) IN GENERAL- The President, in his non-delegable duty, may make an exemption
from this section for a specific use of a chemical substance for a period
not to exceed 5 years if after public notice and comment he determines that--
`(A) an exemption is in the paramount interest of national security, or
if the lack of availability of the chemical substance would cause significant
disruption in the national economy; and
`(B) no feasible alternative for the specified use of the chemical substance
is available.
`(2) RENEWABILITY- The President may renew an exemption under paragraph
(1) for additional 5 year periods if the President concludes after public
comment that such a renewal is necessary.
`(3) PUBLIC NOTICE- A manufacturer of a chemical substance for which an
exemption under this subsection is made shall provide notice of the exemption
to each known customer, and the President shall provide the public with
a notice of such an exemption.
`SEC. 505. ANIMAL TESTING ALTERNATIVES.
`(a) Alternatives to Animal Testing-
`(1) IN GENERAL- To minimize the use of animal testing of chemical substances,
the Administrator shall--
`(A) require the use, where practicable, of--
`(i) existing data to fill data gaps by calling for mandatory disclosure
of all existing data, and thoroughly investigating sources of existing
data;
`(ii) replacement alternatives that--
`(I) do not involve the use of an animal to test the chemical substance;
and
`(II) provide information that is equivalent in scientific quality
to the animal testing method; and
`(iii) reduction alternatives that use fewer animals than conventional
animal-based tests when replacement alternatives are impracticable,
including the use of tests that combine two or more endpoints;
`(B) encourage, where practicable--
`(i) the grouping of similar chemicals into categories to limit testing
to only those chemicals which are representative of the group; and
`(ii) the forming of industry consortia to jointly conduct testing to
avoid duplication of tests; and
`(C) fund research and validation studies to reduce and replace the use
of animal tests as provided in this section.
`(2) LIST OF ALTERNATIVE TESTING METHODS- Not later than 1 year after the
date of enactment of this title, and triennially thereafter, the Administrator,
in consultation with the Interagency Science Advisory Board established
in section 507, shall publish a list of the alternative testing methods
described in paragraph (1).
`(b) Authorization of Appropriations- There is authorized to be appropriated
to carry out this section $5,000,000.
`SEC. 506. SAFER ALTERNATIVES AND GREEN CHEMISTRY.
`(a) Safer Alternatives Program- Within 1 year after the date of enactment
of this title, the Administrator shall establish a program to create market
incentives for the development of safer alternatives to existing chemical
substances. This program shall include, but not be limited to--
`(1) expedited review of new chemical substances for which the manufacturer
submits an alternatives analysis indicating that the new chemical substance
is the safer alternative for a particular use than existing chemical substances
used for the same purpose;
`(2) recognition for a chemical substance found by the Administrator to
be a safer alternative for a particular use by means of a special designation
intended for use in marketing the safer alternative, and periodic public
awards; and
`(3) other incentives as the Administrator considers appropriate to encourage
the development, marketing and use of chemical substances found by the Administrator
to be safer alternatives for the particular uses.
`(b) Green Chemistry Research and Clearinghouse Network-
`(1) IN GENERAL- The Administrator shall establish a network of not less
than 4 green chemistry and technology research and clearinghouse centers,
located in various regions of the United States, to support the development
and adoption of safer alternatives to chemical substances, particularly
chemical substances placed on the priority list.
`(2) REQUIREMENTS- The research and clearinghouse centers described in paragraph
(1) shall--
`(A) provide technical assistance relating to alternatives analysis, green
chemistry, and green technology techniques to small and medium-sized manufacturers
of chemical substances;
`(B) provide technical training relating to alternatives analysis, green
chemistry, and green technology techniques to students and professionals;
`(C) conduct alternatives analysis, green chemistry and green technology
research; and
`(D) provide grants to promote and support the research, development,
adoption and use of alternatives to the activities identified in subparagraphs
(A), (B), and (C).
`(3) AUTHORIZATION OF APPROPRIATIONS- There are authorized to be appropriated
to carry out this subsection--
`(A) for fiscal year 2006, $40,000,000; and
`(B) for each of fiscal years 2007 through 2010, $30,000,000.
`SEC. 507. INTERAGENCY SCIENCE ADVISORY BOARD ON CHILDREN'S HEALTH AND TOXIC
SUBSTANCES.
`(a) In General- Not later than 90 days after the date of enactment of this
title, the Administrator shall form an Interagency Science Advisory Board
on Children's Health and Toxic Substances which shall include at a minimum
representatives from the National Institute of Environmental Heath Sciences,
the Centers for Disease Control and Prevention, the National Toxicology Program,
the National Cancer Institute, the National Tribal Science Council and not
less than 3 centers of children's health at leading universities.
`(b) Purposes- The purposes of the Board shall be to--
`(1) provide independent advice and peer review to the Administrator and
Congress on the scientific and technical aspects of problems and issues
related to the requirement of this title;
`(2) review the scientific and technical basis for the standards, rules,
guidance, and other science-based decisions under this Act and providing
expert consultation and advice to the Administrator; and
`(3) reduce the duplication of the efforts by manufactures to conform with
the requirements of this title, and to reduce animal testing.
`SEC. 508. COOPERATION WITH INTERNATIONAL EFFORTS.
`In cooperation with the Secretary of State and the head of any other appropriate
Federal agency (as determined by the Administrator), the Administrator shall
cooperate with any international effort--
`(1) to develop a common protocol or electronic database relating to chemical
substances; or
`(2) to develop safer alternatives for chemical substances.
`SEC. 509. PUBLIC ACCESS TO INFORMATION.
`(a) Transmission to Administrator- Each Federal agency and Federal institution
shall transmit to the Administrator all information provided to the Federal
agency or institution relating to a hazard of or risk of exposure to a chemical
substance.
`(b) Electronic Database-
`(1) STANDARD- Not later than 180 days after the date of enactment of this
title, the Administrator, in collaboration with interested parties, shall
establish standards for an electronic format for sharing of information
relating to the toxicity and use of, and exposure to, chemical substances.
`(2) DATABASE- Not later than 3 years after the date of enactment of this
title, the Administrator, in collaboration with interested parties, shall
develop, and establish procedures for maintaining, a database in which to
store the information described in paragraph (1).
`(c) Public Access- The Administrator shall make available to the public--
`(1) any information provided to the Administrator relating to the properties
and hazards of a chemical substance; and
`(2) any nonconfidential information, as described in section 510, provided
to the Administrator relating to exposure to the substance.
`(d) Reliable Information- The Administrator shall establish procedures to
ensure data reliability that include--
`(1) not less than 1 time each year, the Administrator shall randomly inspect
not less than 3 percent of the commercial and private laboratories which
develop the data required by the title on the various properties and characteristics
of a chemical substance; and
`(2) annually, the Administrator shall perform a comprehensive data audit
on a statistically significant number of the data submissions submitted
by manufacturers under this title.
`SEC. 510. CONFIDENTIAL BUSINESS INFORMATION.
`(a) In General- If a manufacturer of a chemical substance submits to the
Administrator or any other Federal agency or institution any confidential
business information (as defined in section 350.27 of volume 40, Code of Federal
Regulations, as in effect on the date of enactment of this title), the chief
executive officer shall provide to the Administrator or other Federal agency
or institute--
`(1) a written justification for maintaining the confidentiality of the
information, including, if applicable, a statement that the information
must be kept confidential to protect a trade secret of the manufacturer;
and
`(2) certification that the information is not otherwise publicly available.
`(b) Information From Foreign Countries- Any information provided to the Administrator
by an officer or employee of a foreign government shall be considered to be
confidential business information if the information is considered to be confidential
business information by the officer or employee of the foreign government,
except as described in subsection (c).
`(c) Nonconfidential Information- The name of a chemical substance and all
information concerning its effects on human health or the environment shall
not be considered to be confidential business information under this section.
`SEC. 511. RELATIONSHIP TO OTHER LAW.
`Nothing in this title affects the right of a State or political subdivision
of a State to adopt or enforce any regulation, requirement, liability, or
standard of performance that is more stringent than a regulation, requirement,
liability, or standard of performance established by this title.'.
(b) Effect of Section- Notwithstanding the amendment made by subsection (a)(1),
any regulation promulgated (including any prohibition or restriction issued)
under the provisions repealed by that subsection before the date of enactment
of this Act shall remain in effect until the date on which the Administrator
of the Environmental Protection Agency promulgates new regulations under title
V of the Toxic Substances Control Act (15 U.S.C. 2601 et seq.) (as added by
subsection (a)(2)).
(c) Conforming Amendments-
(1) TESTING OF CHEMICAL SUBSTANCES AND MIXTURES- Section 4 of the Toxic
Substances Control Act (15 U.S.C. 2603) is amended--
(A) in subsection (f), in the matter following paragraph (2), by inserting
`, or title V,' after `section 5, 6, or 7'; and
(B) in subsection (g), by inserting `or title V' after `section 5(a)'.
(2) MANUFACTURING AND PROCESSING NOTICES- Section 5 of the Toxic Substances
Control Act (15 U.S.C. 2604) is amended--
(i) in paragraph (1)(A)(ii), by inserting `or title V' after `section
4'; and
(ii) in paragraph (2)(A)(ii), by inserting `or title V' after `section
4';
(B) in subsection (d)(2)(C), by inserting `or title V' after `section
4';
(C) in subsection (e)(2)(D), in the first sentence, by inserting `or title
V' after `section 6(a)';
(i) in paragraph (1), by inserting `or title V' after `section 6';
(ii) in paragraph (2), in the matter preceding subparagraph (A), by
inserting `or title V' after `section 6(a)'; and
(iii) in paragraph (3)(B), by inserting `or title V' after `section
6'; and
(E) in subsection (g), by inserting `, or title V,' after `section 6 or
7'.
(3) IMMINENT HAZARDS- Section 7 of the Toxic Substances Control Act (15
U.S.C. 2606) is amended--
(i) in paragraph (1), in the matter following subparagraph (C)--
(I) by striking `section 4, 5, 6, or title IV' and inserting `section
4, 5, or 6, or title IV or V,'; and
(II) by striking `section 5 or title IV' and inserting `section 5
or title IV or V'; and
(ii) in paragraph (2), by inserting `title V or' before `section 6(a)';
and
(B) in subsection (f), in the second sentence, by inserting `or title
V' after `section 6'.
(4) REPORTING AND RETENTION OF INFORMATION- Section 8 of the Toxic Substances
Control Act (15 U.S.C. 2607) is amended--
(A) in subsection (a)(3)(A)(ii)--
(i) in subclause (I), by inserting `or title V' after `or 6,'; and
(ii) in subclause (II), by inserting `or title V' after `section 5 or
7'; and
(B) in subsection (b)(1)--
(i) in the first sentence, by striking `section 5 or subsection (a)
of this section' and inserting `subsection (a), section 5, or title
V'; and
(ii) in the second sentence, by inserting `or title V' after `section
5'.
(5) RELATIONSHIP TO OTHER FEDERAL LAWS- Section 9(a) of the Toxic Substances
Control Act (15 U.S.C. 2608(a)) is amended--
(A) in paragraph (2), in the matter following subparagraph (B), by inserting
`or title V' after `section 6 or 7'; and
(B) in paragraph (3), by inserting `or title V' after `section 6 or 7'.
(6) EXPORTS- Section 12 of the Toxic Substances Control Act (15 U.S.C. 2611)
is amended--
(A) in subsection (a)(2), by inserting `or title V' after `section 4';
and
(i) in paragraph (1), by inserting `or title V' after `section 4 or
5(b)'; and
(I) by inserting `or title V' after `issued under section 5';
(II) by inserting `or title V' after `section 5 or 6'; and
(III) by inserting `or title V' after `section 5 or 7'.
(7) ENTRY INTO CUSTOMS TERRITORY OF THE UNITED STATES- Section 13(a)(1)
of the Toxic Substances Control Act (15 U.S.C. 2612(a)(1)) is amended by
striking subparagraph (B) and inserting the following:
`(B) the substance, mixture, or article is offered for entry in violation
of section 5, 6, or 7, or title IV or V.'.
(8) DISCLOSURE OF DATA- Section 14(b)(1)(A)(ii) of the Toxic Substances
Control Act (15 U.S.C. 2613(b)(1)(A)(ii)) is amended by striking `for which
testing' and all that follows through `section 5, and' and inserting `for
which testing or a notification is required under section 4 or 5 or title
V; and'.
(9) PROHIBITED ACTS- Section 15 of the Toxic Substances Control Act (15
U.S.C. 2614) is amended--
(A) by striking paragraph (1) and inserting the following:
`(1) fail or refuse to comply with any rule or requirement under section
4, 5, or 6, or title II or V;'; and
(B) in paragraph (2), by striking `violation of section 5' and all that
follows through `section 5 or 7' and inserting `violation of section 5,
6, or 7, or title V'.
(10) SPECIFIC ENFORCEMENT AND SEIZURE- Section 17(a)(1) of the Toxic Substances
Control Act (15 U.S.C. 2616(a)(1)) is amended--
(A) by striking subparagraph (B) and inserting the following:
`(B) restrain any person from taking an action prohibited under section
5 or 6, or title IV or V;'; and
(B) in subparagraph (D), by striking `in violation' and all that follows
through `title IV' and inserting `in violation of section 5 or 6 or title
IV or V'.
(11) PREEMPTION- Section 18 of the Toxic Substances Control Act (15 U.S.C.
2617) is amended to read as follows:
`SEC. 18. PREEMPTION.
`Nothing in this Act affects the authority of a State or political subdivision
of a State to establish or continue in effect any regulation of a chemical
substance, mixture, or article containing a chemical substance or mixture.'.
(12) JUDICIAL REVIEW- Section 19 of the Toxic Substances Control Act (15
U.S.C. 2618) is amended--
(I) in subparagraph (A), by striking `title II or IV' and inserting
`title II, IV, or V'; and
(II) in subparagraph (B), by inserting `or title V' after `section
6(b)(1)'; and
(ii) in paragraph (3), by striking subparagraph (B) and inserting the
following:
`(B) for a rule or finding under section 4, 5, or 6, or title IV or V,
the finding required for the issuance of the rule;'; and
(B) in subsection (c)(1)(B)--
(i) in clause (i), by inserting `, or title V,' after `6(e)'; and
(ii) in clause (iii)(I), by striking `section 6(c)(1), or' and inserting
`section 6(c)(1) or title V; or'.
(13) CITIZENS' CIVIL ACTIONS- Section 20(a)(1) of the Toxic Substances Control
Act (15 U.S.C. 2619(a)(1)) is amended by striking `title II or IV' and inserting
`title II, IV, or V'.
(14) CITIZENS' PETITIONS- Section 21 of the Toxic Substances Control Act
(15 U.S.C. 2620) is amended--
(A) in subsection (a), by striking `a rule under' and all that follows
through `6(b)(2)' and inserting `a rule or order under section 4, 5, 6,
or 8, or title V'; and
(i) in paragraph (1), by striking ` a rule under' and all that follows
through `6(b)(1)(B)' and inserting `a rule or order under section 4,
5, 6, or 8, or title V';
(ii) in paragraph (3), in the first sentence, by inserting `, or title
V' after `section 4, 5, 6, or 8'; and
(iii) in paragraph (4)(B)--
(I) in the matter preceding clause (i), by striking `section 4' and
all that follows through `6(b)(2)' and inserting `rule or order under
section 4, 5, 6, or 8, or title V';
(II) in clause (i), by striking `a rule under' and all that follows
through `section 5(e)' and inserting `a rule or order under section
4 or 5 or title V'; and
(III) in clause (ii), by striking `under section 6' and all that follows
through `6(b)(2)' and inserting `or order under section 6 or 8 or
title V'.
(15) EMPLOYMENT EFFECTS- Section 24 of the Toxic Substances Control Act
(15 U.S.C. 2623) is amended--
(A) by striking subsection (a) and inserting the following:
`(a) In General- The Administrator shall evaluate, on a continuing basis,
the potential effects on employment (including reductions in employment or
loss of employment from threatened plant closures) of each rule, order, and
requirement under sections 4, 5, and 6, and title V.'; and
(i) in paragraph (1), in the matter following subparagraph (B), by striking
`a rule or order' and all that follows through `section 5 or 6' and
inserting `a rule, order, or requirement under section 4, 5, or 6, or
title V'; and
(ii) in paragraph (2)(B)(ii), by striking `section 6(c)(3), and' and
inserting `section 6(c)(3) and title V; and'.
(16) ADMINISTRATION OF THE ACT- Section 26(b)(1) of the Toxic Substances
Control Act (15 U.S.C. 2625(b)(1)) is amended by inserting `or title V'
after `section 4 or 5' each place it appears.
(17) DEVELOPMENT AND EVALUATION OF TEST METHODS- Section 27(a) of the Toxic
Substances Control Act (15 U.S.C. 2626(a)) is amended by inserting `or title
V' after `section 4' each place it appears.
(18) ANNUAL REPORT- Section 30 of the Toxic Substances Control Act (15 U.S.C.
2629) is amended--
(A) in paragraph (1), by inserting `and title V' after `section 4';
(i) by inserting `or title V' after `section 5';
(ii) by inserting `or title V' after `section 4'; and
(iii) by inserting `or title V' after `section 5(g)'; and
(C) in paragraph (3), by inserting `or title V' after `section 6'.
(19) TABLE OF CONTENTS- The table of contents of the Toxic Substances Control
Act (15 U.S.C. prec. 2601) is amended by adding at the end the following:
`TITLE V--CHILD SAFE CHEMICALS
`Sec. 501. Manufacturer safety certifications.
`Sec. 502. Priority list of chemical substances for EPA safety determination.
`Sec. 503. EPA Safety determination for chemical substances.
`Sec. 504. Reduction of health hazards for children, workers, and consumers.
`Sec. 505. Animal testing alternatives.
`Sec. 506. Safer alternatives and green chemistry.
`Sec. 507. Interagency Science Advisory Board on Children's Health and Toxic
Substances.
`Sec. 508. Cooperation with international efforts.
`Sec. 509. Public access to information.
`Sec. 510. Confidential business information.
`Sec. 511. Relationship to other law.'.
END