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United States Government Accountability Office: 
GAO: 

Testimony: 

Before the Subcommittee on Environment and the Economy, Committee on 
Energy and Commerce, House of Representatives: 

For Release on Delivery: 
Expected at 10:15 a.m. EDT: 
Thursday, June 13, 2013: 

Chemical Regulation: 

Observations on the Toxic Substances Control Act and EPA 
Implementation: 

Statement of Alfredo Gomez, Director: 
Natural Resources and Environment: 

GAO-13-696T: 

GAO Highlights: 

Highlights of GAO-13-696T, a testimony before the Subcommittee on 
Environment and the Economy, Committee on Energy and Commerce, House 
of Representatives. 

Why GAO Did This Study: 

In 1976, Congress passed TSCA to give EPA the authority to obtain more 
health and safety information on chemicals and to regulate chemicals 
it determines pose unreasonable risks of injury to human health or the 
environment. GAO has reported that EPA has found many of TSCA’s 
provisions difficult to implement. In 2009, EPA announced TSCA reform 
principles to inform ongoing efforts in Congress to strengthen the 
act. At that time, EPA also initiated a new approach for managing 
toxic chemicals using its existing TSCA authorities. 

This testimony summarizes GAO’s past work describing: (1) challenges 
EPA has faced historically in regulating chemicals and (2) the extent 
to which EPA has made progress implementing its new approach, and 
challenges, if any, which persist. This statement is based on GAO 
reports issued between 1994 and 2013. 

What GAO Found: 

GAO reported in June 2005 that EPA has historically faced the 
following challenges in implementing the provisions of the Toxic 
Substances Control Act (TSCA): 

* Obtaining adequate information on chemical toxicity and exposure. 
EPA has found it difficult to obtain such information because TSCA 
does not require companies to provide it; instead, TSCA requires EPA 
to demonstrate that chemicals pose certain risks before it can ask for 
such information. 

* Banning or limiting chemicals. EPA has had difficulty demonstrating 
that chemicals should be banned or have limits placed on their 
production or use under section 6—provisions for controlling 
chemicals. The agency issued regulations to ban or limit production or 
use of five existing chemicals, or chemical classes, out of tens of 
thousands of chemicals listed for commercial use. A court reversal of 
EPA’s 1989 asbestos rule illustrates the difficulties EPA has had in 
issuing regulations to control existing chemicals. 

* Disclosing data and managing assertions of confidentiality. EPA has 
not routinely challenged companies’ assertions that data they provide 
are confidential business information and cannot be disclosed. As a 
result, the extent to which companies’ confidentiality claims are 
warranted is unknown. 

GAO reported in March 2013 that EPA has made progress implementing its 
new approach to managing toxic chemicals under its existing TSCA 
authority but, in most cases, results have yet to be realized. 
Examples are as follows: 

* EPA has increased efforts to collect toxicity and exposure data 
through the rulemaking process, but because rules can take 3 to 5 
years to finalize and 2 to 2 ½ years for companies to execute, these 
efforts may take several years to produce results. Specifically, since 
2009, EPA has (1) required companies to test 34 chemicals and provide 
EPA with the resulting toxicity and other data, and (2) announced, but 
has not yet finalized, plans to require testing for 23 additional 
chemicals. 

* EPA has increased efforts to assess chemical risks, but because EPA 
does not have the data necessary to conduct all risk assessments, it 
is too early to tell what, if any, risk management actions will be 
taken. In February 2012, EPA announced a plan that identified and 
prioritized 83 existing chemicals for risk assessment; the agency 
initiated assessments for 7 chemicals in 2012 and announced plans to 
start 18 additional assessments during 2013 and 2014. At its current 
pace, it would take EPA at least 10 years to complete risk assessments 
for the 83 chemicals. 

In addition, it is unclear whether EPA’s new approach to managing 
chemicals will position the agency to achieve its goal of ensuring the 
safety of chemicals. EPA’s Existing Chemicals Program Strategy, which 
is intended to guide EPA’s efforts to assess and control chemicals in 
the coming years, does not discuss how EPA will address identified 
challenges. Consequently, EPA could be investing valuable resources, 
time, and effort without being certain that its efforts will bring the 
agency closer to achieving its goal of ensuring the safety of 
chemicals. 

What GAO Recommends: 

GAO is not making new recommendations in this testimony. In prior 
reports, GAO suggested that Congress consider statutory changes to 
TSCA to give EPA additional authorities to obtain information from the 
chemical industry and shift more of the burden to chemical companies 
for demonstrating the safety of their chemicals. In these reports, 
among other things, GAO recommended that EPA require companies to 
provide chemical data they submitted to foreign governments, require 
companies to reassert confidentiality claims, and develop strategies 
for addressing challenges that impeded EPA’s ability to ensure 
chemical safety. EPA’s responses to these recommendations have varied. 

View [hyperlink, http://www.gao.gov/products/GAO-13-696T]. For more 
information, contact Alfredo Gomez at (202) 512-3841 or gomezj@gao.gov. 

[End of section] 

Chairman Shimkus, Ranking Member Tonko, and Members of the 
Subcommittee: 

I am pleased to be here today to discuss the Environmental Protection 
Agency's (EPA) efforts to assess and control toxic chemicals. Tens of 
thousands of chemicals are listed with EPA for commercial use in the 
United States, with an average of 600 new chemicals listed each year. 
EPA's ability to effectively implement its mission of protecting 
public health and the environment depends on credible and timely 
assessments of the risks posed by toxic chemicals. In 1976, Congress 
passed the Toxic Substances Control Act (TSCA) to provide EPA with the 
authority to obtain more information on chemicals and to regulate 
those chemicals that EPA determines pose unreasonable risks to human 
health or the environment. TSCA authorizes EPA to review chemicals 
already in commerce (existing chemicals) and chemicals yet to enter 
commerce (new chemicals).[Footnote 1] 

We have reported in the past that EPA has found many of the provisions 
of TSCA difficult to implement. In our past reports, we have suggested 
that Congress consider making statutory changes to strengthen EPA's 
authority to obtain toxicity information from the chemical industry 
and establish a framework for taking action that is less burdensome 
for EPA. We have also made several recommendations to better position 
EPA to collect chemical toxicity and exposure-related data and ensure 
chemical safety under existing TSCA authority. Among other 
recommendations, in June 2005,[Footnote 2] we recommended that EPA 
strengthen its ability to regulate harmful chemicals under TSCA by, 
for example, promulgating a rule requiring that companies submit 
copies to EPA of any health and safety studies, as well as other 
information concerning the environmental and health effects of 
chemicals that they submit to foreign governments.[Footnote 3] In that 
report, we also recommended that EPA improve and validate its models 
for assessing and predicting the risks of chemicals and revise its 
regulations to require chemical companies to reassert confidentiality 
claims within a certain period.[Footnote 4] EPA implemented our 2005 
recommendation to improve its models. EPA did not disagree with our 
2005 recommendations regarding obtaining health and safety studies and 
other information that companies submit to foreign governments and 
requiring companies to reassert confidentiality claims, but it 
provided substantive comments and has not fully implemented these 
recommendations. 

In 2009, EPA announced principles for reforming TSCA to help inform 
efforts under way in Congress. These principles include goals for 
reforming TSCA so that: (1) EPA would have clear authority to 
establish safety standards that are based on scientific risk 
assessments; (2) manufacturers' data on toxicity, exposure,[Footnote 
5] and use for chemicals would be required at sufficient levels so 
that EPA could support a determination that a chemical meets the 
safety standard; (3) EPA would have clear authority to take regulatory 
or other actions when chemicals do not meet the safety standard, with 
the flexibility to take into account a range of considerations, 
including children's health, economic costs, social benefits, and 
equity concerns; (4) EPA would have authority to set priorities for 
conducting safety reviews on existing chemicals based on relevant risk 
and exposure considerations; and (5) EPA would receive a sustained 
source of funding from manufacturers of chemicals to support the costs 
of agency implementation, including the review of information provided 
by manufacturers. 

Along with the announcement of these principles in 2009, EPA initiated 
a new approach to managing chemicals within the limits of existing 
authorities that focuses largely on existing chemicals. According to 
agency documents, EPA will transition from an approach dominated by 
voluntary data submissions by industry to a more proactive approach in 
which the agency will use its data collection and other rulemaking 
authorities under TSCA to ensure chemical safety. In February 2012, 
EPA summarized many of the activities it had initiated under its new 
approach in the agency's Existing Chemicals Program Strategy. 
Collectively, these activities address the following four areas: (1) 
collecting toxicity and exposure data, (2) conducting risk 
assessments, (3) discouraging the use of some chemicals, and (4) 
expanding public access to some chemical data. 

In our most recent report in March 2013, we reported on the extent to 
which EPA had made progress implementing its new approach.[Footnote 6] 
We recommended, among other things, that EPA consider promulgating a 
rule requiring chemical companies to report exposure-related data from 
processors to EPA. EPA stated in its comments that downstream chemical 
processors have little exposure-relevant data--which suggests that it 
does not intend to implement that recommendation.[Footnote 7] Because 
EPA has not developed sufficient chemical assessment information to 
limit exposure to many chemicals that may pose substantial health 
risks, among other reasons, in 2009, we added EPA's processes for 
assessing and controlling toxic chemicals to our list of programs at 
high risk of waste, fraud, abuse, and mismanagement.[Footnote 8] 

My testimony today is based on our prior work on EPA's processes for 
assessing and controlling toxic chemicals. Specifically, my statement 
today discusses: (1) challenges EPA has faced historically in 
regulating chemicals and (2) the extent to which EPA has made progress 
implementing its new approach, and challenges, if any, which persist. 
This statement is based on our extensive body of work on TSCA and 
EPA's programs to assess and control chemicals, including reports 
issued from September 1994 to March 2013. Detailed information on our 
scope and methodology is available in each issued product. We 
conducted this work in accordance with generally accepted government 
auditing standards. 

Background: 

Federal laws have been enacted over the years to determine the health 
and environmental hazards associated with toxic chemicals and to 
address these problems. Even with the existence of media-specific 
environmental laws enacted in the early 1970s, such as the Clean Air 
Act and the Clean Water Act, problems with toxic chemicals continued 
to occur. In addition, Congress became increasingly concerned about 
the long-term effects of substantial amounts of chemicals entering the 
environment. 

TSCA was enacted to authorize EPA to collect information about the 
hazards posed by chemical substances and to take action to control 
unreasonable risks by either preventing dangerous chemicals from 
making their way into use or placing restrictions on those already in 
commerce. Under the act, EPA can control the entire life cycle of 
chemicals from their production, distribution in commerce, and use to 
their disposal. Other environmental and occupational health laws 
generally control only disposal or release to the environment, or 
exposures in the workplace. The scope of TSCA includes those chemicals 
manufactured, imported, processed,[Footnote 9] distributed in 
commerce, used, or disposed of in the United States but excludes 
certain substances regulated under other laws.[Footnote 10] TSCA also 
specifies when EPA may publicly disclose chemical information it 
obtains from chemical companies and provides that chemical companies 
can claim certain information, such as data disclosing chemical 
processes, as confidential business information. 

EPA's authority to ensure that chemicals in commerce do not present an 
unreasonable risk of injury to health or the environment is 
established in five major sections of TSCA. The purpose and 
application of these sections are shown in table 1 and described in 
further detail below. 

Table 1: Purpose and Application of TSCA's Major Sections: 

Section: 4; 
Purpose: Chemical testing; 
Provides EPA with a mechanism to: Require companies to develop 
toxicity data under certain circumstances. 

Section: 5; 
Purpose: New chemical review and significant new use rules; 
Provides EPA with a mechanism to: Review existing information, 
including exposure and toxicity data for new chemicals and certain new 
uses of existing chemicals. 

Section: 6; 
Purpose: Control of chemicals; 
Provides EPA with a mechanism to: Limit or ban a chemical, among other 
controls. 

Section: 8; 
Purpose: Industry reporting of chemical data; 
Provides EPA with a mechanism to: Obtain existing data, including 
exposure and toxicity data. 

Section: 14; 
Purpose: Disclosure of chemical data; 
Provides EPA with a mechanism to: Disclose certain data provided to or 
obtained by EPA while also protecting confidential business 
information. 

Source: GAO analysis of TSCA. 

[End of table] 

Under the provisions for chemical testing in section 4 of TSCA, EPA 
can promulgate rules to require chemical companies to test potentially 
harmful chemicals for their health and environmental effects. However, 
EPA must first determine that testing is warranted based on some 
toxicity or exposure information. Specifically, to require such 
testing, EPA must find that a chemical (1) may present an unreasonable 
risk of injury to human health or the environment or (2) is or will be 
produced in substantial quantities and that either (a) there is or may 
be significant or substantial human exposure to the chemical or (b) 
the chemical enters or may reasonably be anticipated to enter the 
environment in substantial quantities. EPA must also determine that 
there are insufficient data to reasonably determine or predict the 
effects of the chemical on health or the environment and that testing 
is necessary to develop such data. 

Under the provisions for new chemical review and significant new use 
rules in section 5 of TSCA, chemical companies are to notify EPA at 
least 90 days before beginning to manufacture a new chemical 
(premanufacture notice review). Section 5 also allows EPA to 
promulgate significant new use rules, which require companies to 
notify EPA at least 90 days before beginning to manufacture a chemical 
for certain new uses or in certain new ways (significant new use 
notice review). Such rules require existing chemicals to undergo the 
same type of review that new chemicals undergo. For example, EPA may 
issue a significant new use rule if it learns that a chemical that has 
previously been processed as a liquid is now being processed as a 
powder, which may change how workers are exposed to the chemical. 
Section 5 of the act also authorizes EPA to maintain a list of 
chemicals--called the chemicals of concern list--that present or may 
present an unreasonable risk of injury to health or the environment. 

Under the provisions for chemical regulation in section 6 of TSCA, EPA 
is to apply regulatory requirements to chemicals for which EPA finds a 
reasonable basis exists to conclude that the chemical presents or will 
present an unreasonable risk of injury to health or the environment. 
To adequately protect against a chemical's risk, EPA can promulgate a 
rule that bans or restricts the chemical's production, processing, 
distribution in commerce, disposal, or use or requires warning labels 
be placed on the chemical. Under TSCA, EPA must choose the least 
burdensome requirement that will adequately protect against the risk. 

Under the provisions for industry reporting of chemical data in 
section 8(a), EPA is to promulgate rules under which chemical 
companies must maintain records and submit such information as the EPA 
Administrator reasonably requires. This information can include, among 
other things, chemical identity, categories of use, production levels, 
by-products, existing data on adverse human health and environmental 
effects, and the number of workers exposed to the chemical, to the 
extent such information is known or reasonably ascertainable. Under 
section 8(a), EPA issues rules to update the TSCA inventory. For 
example, in August 2011, EPA finalized its TSCA Chemical Data 
Reporting rule (previously referred to as the Inventory Update 
Reporting Modifications Rule); the rule requires companies to report, 
among other things, exposure-related information, such as production 
volume and use data, on chemicals manufactured or imported over a 
certain volume per year. In addition, section 8(d) provides EPA with 
the authority to promulgate rules under which chemical companies are 
required to submit lists or copies of existing health and safety 
studies to EPA. Section 8(e) generally requires chemical companies to 
report any information to EPA that reasonably supports a conclusion 
that a chemical presents a substantial risk of injury to health or the 
environment. 

Under the provisions for disclosure of chemical data in section 14, 
EPA may disclose chemical information it obtains under TSCA under 
certain conditions. Chemical companies can claim certain information, 
such as data disclosing chemical processes, as confidential business 
information. EPA generally must protect confidential business 
information against public disclosure unless necessary to protect 
against an unreasonable risk of injury to health or the environment. 
Other federal agencies and federal contractors can obtain access to 
this confidential business information to carry out their 
responsibilities. EPA may also disclose certain data from health and 
safety studies. 

Historical Challenges EPA Has Faced Regulating Chemicals under TSCA: 

We have previously reported that EPA has historically faced challenges 
implementing many of the provisions of TSCA, in particular (1) 
obtaining adequate information on chemical toxicity and exposure 
through testing provisions; (2) banning or limiting chemicals; and (3) 
disclosing chemical data and managing company assertions of 
confidentiality. 

Obtaining Adequate Information on Chemical Toxicity and Exposure: 

EPA has found it difficult to obtain adequate information on chemical 
toxicity and exposure because TSCA does not require companies to 
provide this information and, instead, requires EPA to demonstrate 
that chemicals pose certain risks before it can ask for such 
information. 

Specifically, we reported in 2005 that under section 4--provisions for 
chemical testing--EPA has found its authority to be difficult, time-
consuming, and costly to use.[Footnote 11] The structure of this 
section places the burden on EPA to demonstrate certain health or 
environmental risks before it can require companies to further test 
their chemicals. While TSCA authorizes EPA to review existing 
chemicals, it generally provides no specific requirement, time frame, 
or methodology for doing so. Instead, EPA conducts initial reviews 
after it receives information from the public or chemical companies 
that a chemical may pose a risk. As a result, EPA has only limited 
information on the health and environmental risks posed by these 
chemicals. In our June 2005 report, we suggested that Congress 
consider amending TSCA to provide explicit authority for EPA to enter 
into enforceable consent agreements under which chemical companies are 
required to conduct testing, and give EPA, in addition to its current 
authorities under section 4 of TSCA, the authority to require chemical 
substance manufacturers and processors to develop test data based on 
substantial production volume and the necessity for testing. 

In addition, we reported in June 2005 that under section 5--provisions 
for new chemical review--TSCA generally requires chemical companies to 
submit a notice to EPA (known as a "premanufacture notice") before 
they manufacture or import new chemicals and to provide any available 
test data. EPA estimated that most notices do not include any test 
data and that about 15 percent of them included health or safety test 
data. These tests may take over a year to complete and cost hundreds 
of thousands of dollars, and chemical companies usually do not perform 
them voluntarily. However, chemical companies are not generally 
required under TSCA to limit the production of a chemical or its uses 
to those specified in the premanufacture notice or to submit another 
premanufacture notice if changes occur. For example, companies may 
increase production levels or expand the uses of a chemical, 
potentially increasing the risk of injury to human health or the 
environment. 

Banning or Limiting Chemicals: 

EPA has had difficulty demonstrating that chemicals should be banned 
or have limits placed on their production or use under section 6--
provisions for controlling chemicals. Specifically, we reported, in 
June 2005, that since Congress enacted TSCA in 1976,[Footnote 12] EPA 
has issued regulations under section 6 to ban or limit the production 
or restrict the use of five existing chemicals or chemical classes out 
of tens of thousands of chemicals listed for commercial use on the 
agency's TSCA inventory.[Footnote 13] 

EPA's 1989 asbestos rule illustrates the difficulties EPA has had in 
issuing regulations to control existing chemicals. In 1979, EPA 
started considering rulemaking on asbestos. After concluding that 
asbestos was a potential carcinogen at all levels of exposure, 
[Footnote 14] EPA promulgated a rule in 1989 prohibiting the future 
manufacture, importation, processing, and distribution of asbestos in 
almost all products. Some manufacturers of asbestos products filed 
suit against EPA, arguing, in part, that the rule was not promulgated 
on the basis of substantial evidence regarding unreasonable risk. In 
1991, the Fifth Circuit Court of Appeals ruled for the manufacturers 
and returned parts of the rule to EPA for reconsideration. In reaching 
this conclusion, the court found that EPA did not consider all 
necessary evidence and failed to show that the control action it chose 
was the least burdensome reasonable regulation required to adequately 
protect human health or the environment. Since the court's 1989 
decision, EPA has only exercised its authority to ban or limit the 
production or use of an existing chemical once--for hexavalent 
chromium, a known human carcinogen widely used in industrial cooling 
towers--in 1990.[Footnote 15] 

Disclosure of Chemical Data: 

EPA has limited ability to publicly share the information it receives 
from chemical companies under TSCA. Specifically, as we reported in 
2005, EPA has not routinely challenged companies' assertions that the 
chemical data they disclose to EPA under section 14--disclosure of 
chemical data--are confidential business information, citing resource 
constraints. TSCA requires EPA to protect trade secrets and privileged 
or confidential commercial or financial information against 
unauthorized disclosures. When information is claimed as confidential 
business information, it limits EPA's ability to expand public access 
to this information--such as sharing it with state environmental 
agencies and foreign governments, which potentially limits the 
effectiveness of these organizations' environmental risk programs. 

Because EPA has not routinely challenged these assertions, the extent 
to which companies' confidentiality claims are warranted is unknown. 
We recommended, in June 2005, that EPA revise its regulations to 
require that companies periodically reassert claims of 
confidentiality.[Footnote 16] EPA did not disagree with our 
recommendation but has not revised its regulations. EPA has explored 
ways to reduce the number of inappropriate and over-broad claims of 
confidentiality by companies that submit data to EPA. 

EPA Has Made Progress to Implement Its New Approach to Managing 
Chemicals, but Some Challenges Persist: 

In March 2013, we reported on progress EPA has made implementing its 
new approach to manage toxic chemicals under its existing TSCA 
authority--particularly by increasing efforts to (1) obtain toxicity 
and exposure data, (2) assess risks posed by chemicals, and (3) 
discourage the use of some chemicals.[Footnote 17] However, the 
results of EPA's activities, in most cases, have yet to be realized. 
We also reported that it is unclear whether EPA's new approach will 
position the agency to achieve its goal of ensuring the safety of 
chemicals. 

EPA Has Increased Efforts to Collect Data on Toxicity and Exposure, 
but It May Take Several Years to Produce Results: 

EPA has increased its efforts to collect toxicity and exposure data, 
but because rules can take years to finalize and additional time for 
companies to execute, these efforts may take several years to produce 
results. Even with these efforts, EPA has not pursued all 
opportunities to obtain chemical data. 

We reported, in March 2013, that EPA has made progress by taking the 
following actions but continues to face challenges in collecting such 
data, specifically: 

* Since 2009, EPA has proposed or promulgated rules to require 
chemical companies to test 57 chemicals. Specifically, EPA has 
required companies to test 34 chemicals and provide EPA with the 
resulting toxicity and other data. In addition, EPA announced, but has 
yet to finalize,[Footnote 18] plans to require testing for 23 
additional chemicals.[Footnote 19] However, requirements under TSCA 
place the burden of developing toxicity data on EPA. Because 
rulemaking can take years, EPA has yet to obtain much of the 
information it has been seeking. According to EPA officials, it can 
take, on average, 3 to 5 years for the agency to promulgate a test 
rule and an additional 2 to 2 ½ years for the companies to provide the 
data once EPA has requested them. In addition, the toxicity data 
eventually obtained on the 57 chemicals may not be sufficient for EPA 
to conduct a risk assessment (i.e., characterize risk by determining 
the probability that populations or individuals so exposed to a 
chemical will be harmed and to what degree). Specifically, EPA may 
obtain data that are considered to be "screening level" information. 
Screening level information is collected to identify a chemical's 
potential hazards to human health and the environment, but it was not 
intended to be the basis for assessing whether a chemical poses an 
unreasonable risk of injury to human health or the environment, 
according to agency documents describing the program. 

* In August 2011, EPA revised its periodic chemical data reporting 
requirements to obtain exposure-related information for a greater 
number of chemicals. Under the revised requirements, EPA (1) lowered 
the reporting thresholds, in some cases,[Footnote 20] which will allow 
it to look at exposure scenarios for a larger number of chemicals than 
in the past and (2) shortened the reporting cycle from every 5 years 
to every 4 years. In addition, starting in 2016, the revised 
requirements for reporting will be triggered when companies exceed 
applicable production thresholds in any year during the 4-year 
reporting cycle.[Footnote 21] 

Even with the increased efforts EPA has taken to collect toxicity and 
exposure data, in March 2013, we reported that EPA has not pursued all 
opportunities to obtain such data. For example, EPA has not sought 
toxicity and exposure data that companies submit to the European 
Chemicals Agency on chemicals that the companies manufacture or 
process in, or import to, the United States.[Footnote 22] Under the 
European Union's chemicals legislation, the European Chemicals Agency 
may share information it receives from chemical companies with foreign 
governments in accordance with a formal agreement concluded between 
the European Community and the foreign government, but EPA has not 
pursued such an agreement. In addition, EPA has not issued a rule 
under section 8 of TSCA requiring companies to provide EPA with the 
information provided to the European Chemicals Agency. EPA officials 
told us that the agency has not sought to obtain chemical data--from 
either the European Chemicals Agency or companies directly--because it 
does not believe that this would be the best use of EPA or industry 
resources. They also said that it is unclear whether these data would 
be useful to EPA. EPA officials believe it is a more effective use of 
resources to gain access to data, as needed, on a case-by-case basis 
from chemical companies. As a result, we recommended that EPA consider 
promulgating a rule under TSCA section 8, or take action under another 
section, as appropriate, to require chemical companies to report 
chemical toxicity and exposure-related data they have submitted to the 
European Chemicals Agency. In its written comments on a draft of our 
March 2013 report, EPA stated that it intends to pursue data submitted 
to the European Chemicals Agency from U.S. companies using voluntary 
or regulatory means as necessary but did not provide information on 
its planned approach to pursue such data. Consequently, the extent to 
which EPA plans to continue to rely on voluntary efforts to obtain the 
needed data is unclear. 

EPA Has Begun Assessing Chemical Risks, but It Is Too Early to Tell 
What, If Any, Risk Management Actions Will Be Taken: 

EPA has increased its efforts to assess chemical risks, but because 
EPA does not have the data necessary to conduct all risk assessments, 
it is too early to tell what, if any, risk management actions will be 
taken. Even with these efforts, it is unclear how EPA is going to 
obtain the data necessary to continue to conduct all risk assessments. 

We reported, in March 2013, that EPA has made progress to assess 
chemical risks by taking the following actions but continues to face 
challenges. Specifically, in February 2012, EPA announced a plan that 
identified and prioritized 83 existing chemicals for risk assessment--
known as the TSCA Work Plan.[Footnote 23] From this list of 83 
chemicals, EPA's Office of Pollution Prevention and Toxics--the office 
responsible for implementing TSCA--initiated risk assessments for 7 
chemicals in 2012--5 of which were released for public comment--and 
announced plans to start risk assessments during 2013 and 2014 for 18 
additional chemicals.[Footnote 24] EPA officials told us that they 
expect that all 7 risk assessments will be finalized early in 2014. 
However, it may be years before EPA initiates regulatory or other risk 
management actions to reduce any chemical risks identified in these 
assessments. Before EPA can determine such actions are warranted, the 
agency would need to consider other factors--such as costs and 
benefits of mitigating the risk, technological information, and the 
concerns of stakeholders--which could require additional time and 
resources. Moreover, assuming EPA meets its 2014 target for completing 
these 7 assessments and initiating new assessments, at its current 
pace, it would take EPA at least 10 years to complete risk assessments 
for the 83 chemicals in the TSCA Work Plan. 

As we reported, in March 2013, even with these increased efforts, it 
is unclear whether EPA can maintain its current pace given that it 
currently does not have the toxicity and exposure data it will need to 
conduct risk assessments for all of the 83 chemicals in its TSCA Work 
Plan. According to EPA officials and agency documents, the agency has 
started or plans to start risk assessments on the 25 chemicals for 
which it has well-characterized toxicity and exposure data. However, 
before EPA can initiate risk assessments for the remaining 58 
chemicals, the agency will need to identify and obtain toxicity and 
exposure data. According to agency officials, to obtain the toxicity 
data needed, EPA may need to promulgate rules to require companies to 
perform additional testing on some of these chemicals. However, EPA 
has not clearly articulated how or when it plans to obtain these 
needed data. Moreover, without exposure-related data, such as those 
potentially available from chemical processors, EPA may still be 
missing the data necessary to conduct risk assessments. To better 
position EPA to ensure chemical safety under existing TSCA authority, 
in our March 2013 report we recommended that EPA develop strategies 
for addressing challenges associated with obtaining toxicity and 
exposure data needed for risk assessments. However, based on EPA's 
written response to a draft of our 2013 report, it is unclear what 
action, if any, EPA intends to pursue. 

EPA Has Taken Actions That May Discourage the Use of Certain 
Chemicals, but It Is Too Early to Tell Whether These Actions Will 
Reduce Chemical Risk: 

EPA has taken actions that may discourage the use of certain 
chemicals, but because many of these actions have yet to be finalized, 
it is too early to tell whether they will reduce chemical risk. We 
reported in March 2013 that, given the difficulty that EPA has faced 
in the past using section 6 of TSCA to ban existing toxic chemicals or 
place limits on their production or use, the agency generally 
considers using this authority only after exhausting all other 
available options. Since 2009, EPA has made progress by increasing its 
use of certain options, including (1) making greater use of 
significant new use rules under section 5 and (2) proposing actions 
that use its TSCA authority in new ways as follows: 

* EPA is making greater use of significant new use rules under section 
5 to control new uses of existing chemicals. Our analysis of TSCA 
rulemaking from 2009 to 2012 shows that EPA has quadrupled its 
issuance of significant new use rules since 2009. From 2009 to 2012, 
EPA issued significant new use rules affecting about 540 chemicals, 
about 25 percent of all 2,180 chemicals subject to significant new use 
rules issued by EPA since 1976. EPA officials told us that EPA 
typically recommends that companies submit testing information when 
they notify EPA of their intent to manufacture or process chemicals, 
which enables EPA to better evaluate the potential risks associated 
with the new use. According to EPA officials, this approach allows the 
agency to "chip away" at chemicals that may pose risks to human health 
and the environment. Such recommendations may discourage companies 
from pursuing new uses of existing chemicals that may pose health or 
environmental risks either because testing itself can be expensive, or 
because the testing recommendation suggests that the agency may 
consider banning or limiting the manufacture or production of the 
chemical on the basis of that testing. 

* EPA has also proposed actions that use its TSCA authority in new 
ways including the following: 

- Creating "chemicals of concern" list. In May 2010, EPA announced 
that it intended to create a list of chemicals that present or may 
present "an unreasonable risk of injury to health or the environment." 
EPA has had the authority to create such a list under section 5 of 
TSCA since its enactment in 1976 but has never attempted to use this 
authority. EPA submitted the list, which consists of three groups of 
chemicals, for review by the Office of Management and Budget (OMB) in 
May 2010, and as of May 2013, EPA's proposed "chemicals of concern" 
list has been under review at OMB for over 1,000 days and remains 
listed as pending review by OMB.[Footnote 25] 

- Pairing of test and significant new use rules. In December 2010, EPA 
submitted to OMB for review a proposal to pair testing rules with 
significant new use rules for the first time. Specifically, EPA has 
proposed single rules that combine provisions requiring companies to 
develop toxicity and other data with provisions requiring companies to 
provide data for new uses of chemicals. EPA has proposed using this 
approach in two cases. In one case, for example, EPA proposed this 
approach for certain flame retardants that are being voluntarily 
phased out, effective December 2013. Under the proposed rule, any new 
use of the chemical after it has been phased out would qualify as a 
significant new use, triggering a testing requirement. According to 
EPA officials, the pairing of these types of rules is intended to 
discourage new uses of certain chemicals that may pose a risk to human 
health or the environment and create a disincentive for companies to 
continue current use of the chemical--something EPA has not done 
before. OMB's review of this proposal took 422 days and was completed 
on February 15, 2012. 

- Extending significant new use rules to articles. Since 2009, EPA has 
made increasing use of its ability to subject chemicals contained in 
certain products, or "articles," such as furniture, textiles, and 
electronics, to significant new use rules. Generally, those who import 
or process a substance as part of a product are exempted from 
compliance with a significant new use rule. EPA's proposals would 
eliminate this exemption for certain chemicals.[Footnote 26] 

However, it is too early to assess the impact of EPA's proposed 
actions because they have yet to be finalized. In addition, in some 
cases, OMB has not met the established 90-day time for reviewing EPA's 
proposed actions--which has increased the time frames for formally 
proposing and finalizing them.[Footnote 27] In particular, the period 
for OMB review is generally limited by executive order to 90 days, 
although it can be extended. [Footnote 28] 

It Is Unclear Whether EPA's New Approach Will Position the Agency to 
Achieve Its Goal of Ensuring the Safety of Chemicals: 

As we reported in March 2013, it is unclear whether EPA's new approach 
to managing chemicals within its existing TSCA authorities will 
position the agency to achieve its goal of ensuring the safety of 
chemicals. EPA officials have said that the agency's new approach, 
initiated in 2009 and summarized in its 2012 Existing Chemicals 
Program Strategy, is intended to guide EPA's efforts to assess and 
control chemicals in the coming years. However, EPA's strategy, which 
largely focuses on describing activities EPA has already begun, does 
not discuss how it will address challenges discussed earlier 
associated with obtaining toxicity and exposure data and banning or 
limiting the use of chemicals as follows: 

* Obtaining toxicity and exposure data. EPA's strategy does not 
discuss how the agency will meet the challenge we described related to 
obtaining the toxicity and exposure data it will need to conduct all 
risk assessments. In particular, as discussed previously, EPA has not 
broadly sought toxicity and exposure data that companies submit to 
foreign governments; instead EPA plans to obtain these data on a case-
by-case basis from chemical companies. However, the agency's strategy 
does not discuss how EPA would execute these plans or how the data 
obtained would be used to inform the agency's ongoing or future risk 
assessment activities, if at all. 

* Banning or limiting the use of chemicals. EPA's strategy does not 
articulate how the agency would overcome the regulatory challenges it 
experienced in the past. In particular, EPA officials told us that, 
even if EPA has substantial toxicity and exposure data, the agency is 
challenged in meeting the statutory requirement under section 6 of 
TSCA to limit or ban chemicals. 

Further, EPA's strategy does not identify the resources needed to meet 
its goal of ensuring chemical safety. For example, EPA's strategy does 
not identify the resources needed to carry out risk assessment 
activities, even though risk assessment is a central part of EPA's 
effort to manage chemicals under its new approach. Specifically, EPA 
does not identify roles and responsibilities of key staff or offices--
for example which office within EPA will develop the toxicity 
assessments needed to support its planned risk assessments--or 
identify staffing levels or cost associated with conducting its risk 
assessment activities. Without a clear understanding of the resources 
needed to complete risk assessments and other activities identified in 
its strategy, EPA cannot be certain that its current funding and 
staffing levels are sufficient to execute its new approach to managing 
chemicals under existing TSCA authorities. 

When developing new initiatives, agencies can benefit from following 
leading practices for federal strategic planning.[Footnote 29] Of 
these leading practices, it is particularly important for agencies to 
define strategies that address management challenges that threaten 
their ability to meet long-term goals. In our March 2013 report, 
[Footnote 30] we stated that without a plan that incorporates leading 
strategic planning practices--particularly a plan that clearly 
articulates how EPA will address management challenges--EPA cannot be 
assured that it its new approach to managing chemicals, as described 
in its Existing Chemicals Program Strategy, will provide a framework 
to effectively guide its efforts. Consequently, EPA could be investing 
valuable resources, time, and effort without being certain that its 
efforts will bring the agency closer to achieving its goal of ensuring 
the safety of chemicals. As a result, we recommended that the EPA 
Administrator direct the appropriate offices to develop strategies for 
addressing challenges that impede the agency's ability to meet its 
goal of ensuring chemical safety to better position EPA to ensure 
chemical safety under its existing TSCA authority. In its written 
response to our March 2013 report,[Footnote 31] EPA's Acting Assistant 
Administrator stated that change is needed in every significant aspect 
of the program, and, while strategic planning is a useful exercise it 
cannot substitute for the basic authorities needed for a modern, 
effective chemicals program. Moreover, the Acting Assistant 
Administrator stated that it is EPA's position that, absent statutory 
changes to TSCA, the agency will not be able to successfully meet the 
goal of ensuring chemical safety now and into the future. 

Chairman Shimkus, Ranking Member Tonko, and Members of the 
Subcommittee, this concludes my prepared statement. I would be happy 
to respond to any questions that you or Members of the Subcommittee 
may have at this time. 

GAO Contact and Staff Acknowledgments: 

If you or your staff members have any questions about this testimony, 
please contact me at (202) 512-3841 or gomezj@gao.gov. Contact points 
for our Offices of Congressional Relations and Public Affairs may be 
found on the last page of this statement. Other individuals who made 
key contributions include Diane LoFaro, Assistant Director; Diane 
Raynes, Assistant Director; Elizabeth Beardsley; Richard Johnson; 
Alison O'Neill; and Aaron Shiffrin. 

[End of section] 

Related GAO Products: 

Toxic Substances: EPA Has Increased Efforts to Assess and Control 
Chemicals but Could Strengthen Its Approach, [hyperlink, 
http://www.gao.gov/products/GAO-13-249] (Washington, D.C.: Mar. 22, 
2013). 

Chemical Regulation: Observations on Improving the Toxic Substances 
Control Act. [hyperlink, http://www.gao.gov/products/GAO-10-292T]. 
Washington, D.C.: December 2, 2009. 

Chemical Regulation: Options for Enhancing the Effectiveness of the 
Toxic Substances Control Act. [hyperlink, 
http://www.gao.gov/products/GAO-09-428T]. Washington, D.C.: February 
26, 2009. 

High-Risk Series: An Update. [hyperlink, 
http://www.gao.gov/products/GAO-09-271]. Washington, D.C.: January 22, 
2009. 

Toxic Chemicals: EPA's New Assessment Process Will Increase Challenges 
EPA Faces in Evaluating and Regulating Chemicals. [hyperlink, 
http://www.gao.gov/products/GAO-08-743T]. Washington, D.C.: April 29, 
2008. 

Chemical Regulation: Comparison of U.S. and Recently Enacted European 
Union Approaches to Protect against the Risks of Toxic Chemical. 
[hyperlink, http://www.gao.gov/products/GAO-07-825]. Washington, D.C.: 
August 17, 2007. 

Chemical Regulation: Actions Are Needed to Improve the Effectiveness 
of EPA's Chemical Review Program. [hyperlink, 
http://www.gao.gov/products/GAO-06-1032T]. Washington, D.C.: August 2, 
2006. 

Chemical Regulation: Approaches in the United States, Canada, and the 
European Union. [hyperlink, http://www.gao.gov/products/GAO-06-217R]. 
Washington, D.C.: November 4, 2005. 

Chemical Regulation: Options Exist to Improve EPA's Ability to Assess 
Health Risks and Manage Its Chemical Review Program. [hyperlink, 
http://www.gao.gov/products/GAO-05-458]. Washington, D.C.: June 13, 
2005. 

Toxic Substances: EPA Should Focus Its Chemical Use Inventory on 
Suspected Harmful Substances. [hyperlink, 
http://www.gao.gov/products/GAO/RCED-95-165]. Washington, D.C.: July 
7, 1995. 

Toxic Substances Control Act: Legislative Changes Could Make the Act 
More Effective. [hyperlink, 
http://www.gao.gov/products/GAO/RCED-94-103]. Washington, D.C.: 
September 26, 1994. 

Toxic Substances: EPA's Chemical Testing Program Has Not Resolved 
Safety Concern. [hyperlink, 
http://www.gao.gov/products/GAO/RCED-91-136]. Washington, D.C.: June 
19, 1991. 

Toxic Substances: EPA's Chemical Testing Program Has Made Little 
Progress. [hyperlink, http://www.gao.gov/products/GAO/RCED-90-112]. 
Washington, D.C.: April 25, 1990. 

EPA's Efforts To Identify and Control Harmful Chemicals in Use. 
[hyperlink, http://www.gao.gov/products/GAO/RCED-84-100]. Washington, 
D.C.: June 13, 1984. 

[End of section] 

Footnotes: 

[1] Existing chemicals are composed of those that were in commerce in 
1979 when EPA began reviewing chemicals, as well as those listed for 
commercial use after that time. 

[2] GAO, Chemical Regulation: Options Exist to Improve EPA's Ability 
to Assess Health Risks and Manage Its Chemical Review Program, 
[hyperlink, http://www.gao.gov/products/GAO-05-458] (Washington, D.C.: 
June 13, 2005). 

[3] Throughout this testimony, the phrase "chemical companies" refers 
generally to companies that manufacture, import, process, distribute 
in commerce, use, or dispose of chemicals regulated under TSCA. When 
it is important to differentiate between, for example, manufacturers 
and processors, the type of company to which I am referring is 
specified. 

[4] As described later in this testimony, TSCA contains provisions for 
governing the disclosure of chemical data. Chemical companies can 
claim certain information, such as data disclosing chemical processes, 
as confidential business information. 

[5] In this testimony, exposure represents the magnitude, frequency, 
and duration of contact with a chemical. Toxicity represents the 
degree to which a chemical is harmful. In this testimony, the terms 
toxicity and hazard are used synonymously. 

[6] GAO, Toxic Substances: EPA Has Increased Efforts to Assess and 
Control Chemicals but Could Strengthen Its Approach, [hyperlink, 
http://www.gao.gov/products/GAO-13-249] (Washington, D.C.: Mar. 22, 
2013). 

[7] This position, however, conflicts with EPA's principles for TSCA 
reform, which state that, "EPA's authority to require submission of 
use and exposure information should extend to downstream processors…" 
In addition, EPA officials have said that data from downstream 
processors would provide the agency with a better understanding of 
potential exposure to chemicals, for example, chemical exposure from 
consumer products such as those designed for children. 

[8] GAO, High-Risk Series: An Update. [hyperlink, 
http://www.gao.gov/products/GAO-09-271] (Washington, D.C.: Jan. 22, 
2009). 

[9] Processing refers to the preparation of a chemical substance or 
mixture, after its manufacture, for distribution in commerce. 

[10] Excluded substances include certain nuclear materials, 
pesticides, food, food additives, tobacco, drugs, and cosmetics. 

[11] [hyperlink, http://www.gao.gov/products/GAO-05-458]. 

[12] [hyperlink, http://www.gao.gov/products/GAO-05-458]. 

[13] TSCA requires EPA to compile, keep current, and publish a list of 
each chemical substance that is manufactured or processed in the 
United States, which is called the TSCA inventory. Of the over 84,000 
chemicals currently on the TSCA inventory, approximately 8,000 
chemicals are produced at annual volumes of 25,000 pounds or greater. 

[14] EPA came to this conclusion after reviewing over 100 studies of 
the health risks of asbestos, as well as public comments on the 
proposed rule. 

[15] However, EPA officials said that they had started the process for 
promulgating the rule for hexavalent chromium years prior to the 
asbestos decision. 

[16] [hyperlink, http://www.gao.gov/products/GAO-05-458]. 

[17] [hyperlink, http://www.gao.gov/products/GAO-13-249]. 

[18] Final rules are located at 40 C.F.R. §§ 799.5087 and 799.5089 
(2012). The proposed rule is located at 76 Fed. Reg. 65580 (Oct. 21, 
2011). 

[19] By comparison, EPA required testing for fewer than 200 chemicals 
from the time TSCA was enacted in 1976 until 2009 when the agency 
undertook its new approach to managing chemicals. The 57 chemicals 
that are part of EPA's current and proposed testing requirements were 
identified but not sponsored as part of the agency's 1998 voluntary 
effort to obtain testing data from companies on chemicals produced or 
imported at high volumes (i.e., amounts of 1 million pounds or more a 
year). 

[20] For example, the production threshold for providing processing 
and use information went from 300,000 pounds or more to 100,000 pounds 
or more in 2012 and will be reduced to 25,000 pounds thereafter. 

[21] Previously, the reporting requirement was triggered only if 
production levels were exceeded during the reporting year. According 
to EPA officials, this change was important because, under the 
previous requirement, production volumes of chemical substances 
fluctuated above and below reporting thresholds in different reporting 
periods, resulting in a change of approximately 30 percent in the 
composition of the chemical substances reported as being produced from 
one reporting period to the next. 

[22] The European Chemicals Agency implements the European Union's 
chemicals legislation. The European Union's chemicals legislation 
requires companies to develop information on chemicals' effects on 
human health and the environment before entering commerce, while TSCA 
does not require companies to develop such information absent EPA 
rulemaking requiring them to do so. 

[23] In 2011, EPA convened a stakeholder meeting to discuss proposed 
screening criteria and data sources and took public comment over a 35-
day period. Based on the input received, EPA devised and executed a 
protocol that used a combination of risk factors and other criteria. 
Using this protocol, EPA winnowed an initial group of 1,235 chemicals 
down to 83. 

[24] 78 Fed. Reg. 1856 (Jan. 9, 2013). 

[25] These three groups are: (1) a category of eight phthalates, (2) a 
category of polybrominated diphenylethers (PBDE), and (3) bisphenol A 
(BPA). 

[26] In spring 2012, EPA proposed three significant new use rules that 
would require companies to report new uses of five groups of 
chemicals, including in domestic and imported articles. EPA has used 
this approach before but infrequently. EPA first eliminated the 
article exemption for a chemical substance in 1991, when it 
promulgated a significant new use rule for erionite fiber, and it used 
the same approach for a significant new use rule pertaining to the use 
of elemental mercury in certain switches in 2007. 

[27] Any rules that EPA plans to issue under TSCA that are considered 
significant regulatory actions, as defined by Executive Order 12866, 
are subject to review by the Office of Information and Regulatory 
Affairs, an office within OMB, prior to being proposed in the Federal 
Register. Among other things, a significant regulatory action may have 
an annual effect on the economy of $100 million or more or raise novel 
legal or policy issues. 

[28] Under Executive Order 12866, the review period may be extended by 
the head of the rulemaking agency, and the OMB Director may extend the 
review period once for no more than 30 days. 

[29] The strategic planning elements established under the Government 
Performance and Results Act (GPRA) of 1993 and associated OMB guidance 
and practices we identified, taken together, can serve as leading 
practices for strategic planning at lower levels within federal 
agencies, such as planning for individual divisions, programs, or 
initiatives. Leading practices in federal strategic planning include 
defining mission and goals, involving leadership and stakeholders, 
developing performance measures, and developing strategies to address 
management challenges and resources needed, among others. See GAO, 
Environmental Justice: EPA Needs to Take Additional Actions to Help 
Ensure Effective Implementation, [hyperlink, 
http://www.gao.gov/products/GAO-12-77] (Washington, D.C.: Oct. 6, 
2011); see GAO, Environmental Protection: EPA Should Develop a 
Strategic Plan for Its New Compliance Initiative, [hyperlink, 
http://www.gao.gov/products/GAO-13-115] (Washington, D.C.: Dec. 10, 
2012). 

[30] [hyperlink, http://www.gao.gov/products/GAO-13-249]. 

[31] [hyperlink, http://www.gao.gov/products/GAO-13-249]. 

[End of section] 

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