EPA’s Endocrine Disruptor Screening Program Has Made Limited Progress in Assessing Pesticides

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Report Contributors: Natasha Henry
Lauretta Joseph
Michael Wilson
Erin Barnes-Weaver
Abbreviations
C.F.R.
Code of Federal Regulations
CMP
Comprehensive Management Plan
EDSP
Endocrine Disruptor Screening Program
EPA
U.S. Environmental Protection Agency
FFDCA
Federal Food, Drug, and Cosmetic Act
FQPA
Food Quality Protection Act
OCSPP
Office of Chemical Safety and Pollution Prevention
OIG
Office of Inspector General
OPP
Office of Pesticide Programs
WoE
Weight-of-Evidence
Cover Photo: Green frogs collected for evaluation on potential effects of endocrine-
disrupting chemicals. (U.S. Geological Survey image)
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,-^eD svv,. 21-E-0186
U.S. Environmental Protection Agency July 28,2021
\ Office of Inspector General
IWJ
At a Glance
Why We Did This Evaluation
We performed this evaluation to
determine the progress of the
U.S. Environmental Protection
Agency's implementation of
Section 408(p)(3)(A) of the
Federal Food, Drug, and
Cosmetic Act, as amended by
the Food Quality Protection Act,
which requires the EPA to test all
pesticide chemicals for human
endocrine-disruption activity. We
also sought to determine
compliance with
Section 408(p)(6), which
requires the EPA to take action if
it finds, after testing and
evaluation, that a substance
disrupts the human endocrine
system.
Endocrine systems regulate
biological processes in humans
and animals. Endocrine
disruptors are chemicals found in
many products that mimic, block,
or disrupt the normal function of
hormones. The EPA developed
its Endocrine Disruptor
Screening Program in 1998.
This evaluation addresses the
following:
• Ensuring the safety of
chemicals.
This evaluation addresses these
top EPA management challenges:
• Communicating risks.
• Complying with key internal
control requirements (risk
assessments).
Address inquiries to our public
affairs office at (202) 566-2391 or
OIG WEBCOMMENTS@epa.gov.
List of OIG reports.
EPA's Endocrine Disruptor Screening Program
Has Made Limited Progress in Assessing
Pesticides
What We Found
Twenty-four years after the Food Quality Protection
Act of 1996 amendments were passed, the Office of
Chemical Safety and Pollution Prevention has not
implemented Section 408(p)(3)(A) of the Federal
Food, Drug, and Cosmetic Act to test all pesticide
chemicals for endocrine-disruption activity. In
addition, the OCSPP's Office of Pesticide Programs
recommended in 2015 that 17 pesticides needed
additional testing for endocrine disruption in wildlife
in order to provide the data needed to conduct an
ecological risk assessment, but that
recommendation has not been implemented.
Endocrine Disruptor Screening Program testing
delays are inconsistent with the Federal Food, Drug, and Cosmetic Act, which
directs the EPA to take appropriate action to protect public health if a substance
is found to have an effect on the human endocrine system.
We also found that the EPA does not have controls in place to effectively
implement the EDSP, such as strategic guidance documents or performance
measures. Additionally, the EDSP has not conducted annual internal program
reviews to monitor or assess progress in fulfilling regulatory requirements, and
the EDSP has not effectively communicated with internal and external
stakeholders. Moreover, previous OCSPP leadership provided acceptable
corrective actions to meet the recommendations in a 2011 EPA Office of
Inspector General report regarding the EDSP yet failed to actually implement
those corrective actions beyond an initial period of compliance with them. Lastly,
some EPA staff indicated that they were instructed to function as if the EDSP
was eliminated from the EPA's budget.
Because the EDSP has not had effective internal controls in place since 2015, it
cannot have reasonable assurance that the objectives of the program will be
accomplished and that resources will be allocated efficiently and effectively.
Moreover, an established system of management controls would provide
mechanisms for consistent program operations.
Recommendations and Planned Agency Corrective Actions
We make ten recommendations to the assistant administrator for Chemical
Safety and Pollution Prevention related to testing, strategic planning,
performance measurement, annual reviews, and internal and external
communications. The recommendations are resolved with corrective actions
pending.
Without the required
testing and an effective
system of internal
controls, the EPA
cannot make
measurable progress
toward complying with
statutory requirements
or safeguarding human
health and the
environment against
risks from endocrine-
disrupting chemicals.
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UNITED STATES ENVIRONMENTAL PROTECTION AGENCY
WASHINGTON, D.C. 20460
THE INSPECTOR GENERAL
July 28, 2021
MEMORANDUM
SUBJECT: EPA's Endocrine Disruptor Screening Program Has Made Limited Progress in Assessing
Pesticides
Report No. 21-E-0186
This is our report on the subject evaluation conducted by the Office of Inspector General of the
U.S. Environmental Protection Agency. The project number for this evaluation was QA&E-FY20-0379.
This report contains findings that describe the problems the OIG has identified and corrective actions the
OIG recommends. Final determinations on matters in this report will be made by EPA managers in
accordance with established audit resolution procedures.
The Office of Chemical Safety and Pollution Prevention is responsible for the issues discussed in this
report.
In accordance with EPA Manual 2750, your office provided acceptable planned corrective actions and
estimated milestone dates in response to OIG recommendations. All recommendations are resolved, and
no final response to this report is required. If you submit a response, however, it will be posted on the
OIG's website, along with our memorandum commenting on your response. Your response should be
provided as an Adobe PDF file that complies with the accessibility requirements of Section 508 of the
Rehabilitation Act of 1973, as amended. The final response should not contain data that you do not want
to be released to the public; if your response contains such data, you should identify the data for redaction
or removal along with corresponding justification.
FROM:
Sean W. O'Donnell
TO:
Michal liana Freedhoff, Assistant Administrator
Office of Chemical Safety and Pollution Prevention
We will post this report to our website at www.epa.gov/oig.
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EPA's Endocrine Disruptor Screening 21-E-0186
Program Has Made Limited Progress
in Assessing Pesticides
Table of C
Purpose 1
Background 1
Endocrine Systems and Endocrine Disruptors 1
Endocrine Disruptor Screening Program 2
Internal Controls 7
Responsible Offices 8
Scope and Methodology 8
Results 8
Endocrine Disruptor Testing Has Stalled 9
EDSP Has Not Fully Implemented Effective Internal Controls 12
Conclusions 14
Recommendations 15
Agency Response and OIG Assessment 16
Status of Recommendations and Potential Monetary Benefits 17
Appendices
A Agency Response to Draft Report 18
B Distribution 26
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Purpose
The U.S. Environmental
Protection Agency's Office of
Inspector General conducted this
evaluation to determine the
EPA's progress in implementing
Section 408(p)(3)(A) of the
Federal Food, Drug, and
Cosmetic Act, as amended by the
Food Quality Protection Act,
which requires the EPA to test all pesticide chemicals for human
endocrine-disruption activity. We also sought to determine compliance with
Section 408(p)(6) of the FFDCA, as amended by the FQPA, which requires the
EPA to take action if it finds, after testing and evaluation, that a substance
disrupts the human endocrine system.
Background
Endocrine Systems and Endocrine Disruptors
Endocrine systems, also referred to as
hormone systems, are found in all
mammals, birds, fish, and many other
organisms. The endocrine system
regulates biological processes in the body
from conception through adulthood,
including the development of the brain
and nervous system, the growth and
function of the reproductive system, and
the metabolism and blood-sugar levels.
The female ovaries, male testes,
hypothalamus, pituitary gland, and
thyroid glands are major constituents of
the endocrine system (see Figure 1).
Some hormones in the endocrine system
include estrogens, androgens, and thyroid
hormones. Endocrine disruptors are
chemicals that mimic, block, or
otherwise di srupt the normal function of hormones.
Small disturbances in endocrine function, particularly during certain highly
sensitive stages of the life cycle, such as pregnancy and lactation, can lead to
profound and lasting effects. Adverse endocrine-related effects in humans may
include breast cancer, diabetes, obesity, infertility, and learning disabilities.
Top Management Challenges
This evaluation addresses the foiiowing top
management challenges for the Agency, as identified in
OIG Report No. 20-N-0231. EPA's FYs 2020-2021 Top
Management Challenges, issued July 21, 2020:
• Communicating risks.
• Complying with key internal control requirements
(risk assessments).
Figure 1: Human endocrine system
Hypothalamus
Pituitary gland
Thyroid and
parathyroid
glands
Pineal gland
Thymus
[in female)
Placenta
Testic e —
pregnancy)
(in male}
Pancreas
Adrenal
glands
Source: EPA website. (EPA image)
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Endocrine disruptors are in many products,
including pesticides. A 2016 study published
in The Lancet, a medical journal, found that
annual costs associated with endocrine-
disrupting pesticides in the United States was
$42 billion.
Examples of common endocrine
disruptors include:
• Bisphenol A.
• Perfluoroalkyl and Polyfluoroalkyl
substances.
• Dioxins.
• Phthalates.
Endocrine Disruptor Screening
Program
Source: National Institute of
Environmental Health Sciences.
Based on evidence that certain chemicals may disrupt the endocrine system,
Congress passed amendments to the Safe Drinking Water Act and the FQPA,
which amended the FFDCA, in 1996. The FFDCA, as amended, contains
provisions regarding estrogenic substances, including requirements for the EPA to
evaluate those chemicals for their potential to produce effects similar to those
produced by estrogen in humans or other endocrine effects designated by the
The EPA's Office of Chemical Safety and Pollution Prevention, referred to as the
OCSPP, implements the FQPA, and related portions of the FFDCA, as well as the
Federal Insecticide, Fungicide, and Rodenticide Act. We evaluated the EPA's
progress in implementing and complying with two sections of the FFDCA:
• Section 408(p)(3)(A) on testing of all pesticide chemicals for human
endocrine-disruption activity.
• Section 408(p)(6) on taking appropriate action to protect public health
when finding, through testing and evaluation, that a substance has human
endocrine effects.
In order to meet these statutory mandates, the EPA established the Endocrine
Disruptor Screening and Testing Advisory Committee in October 1996 to
recommend how the EPA's Endocrine Disruptor Screening Program would work.
The committee was composed of representatives from industry, government,
environmental and public health groups, worker safety groups, and academia. The
committee's task was to recommend a screening and testing program that would
provide the Agency with the information needed to make regulatory decisions
about chemicals that disrupt the endocrine system. In August 1998, the committee
issued a final report establishing the framework for the EDSP.
The committee's key recommendations, which the EPA adopted, were that EDSP
screening should:
• Evaluate both human and ecological effects.
• Test for disruption of the estrogen, androgen, and thyroid hormone
EPA.
systems.
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• Evaluate both pesticide and nonpesticide chemicals.
• Implement a tiered approach.
The EDSP, which the EPA created in August 1998, is not the only mechanism
available to the Agency to regulate endocrine-disrupting chemicals. According to
the EPA's August 2010 Report to Congress on Pesticide Licensing and Endocrine
Disruytor Screening Activities, from August 3, 1999, through September 30,
2009, the EPA regulated 79 of the 1,095 pesticides subjected to Federal
Insecticide, Fungicide, and Rodenticide Act regulatory review on the basis of
endocrine effects.
EDSP Prioritization Lists
The EPA's "List of the EDSP Universe of Chemicals" encompasses
approximately 10,000 chemicals, as defined under the 1996 FFDCA and Safe
Drinking Water Act amendments, and as of December 2020, EPA senior staff
reported that 1,315 of those chemicals were pesticides. Since available
resources and laboratory capacity limit the number of chemicals that can be
tested simultaneously, the EPA created lists to prioritize which chemicals to
evaluate first. The EPA published EDSP List 1 in April 2009, which contained
67 pesticides and High Production Volume chemicals used as pesticide inert
ingredients. The EPA later revised this list to 52 chemicals because
15 chemicals were subsequently canceled or discontinued.
In its fiscal year 2010 House Appropriations Committee report. Congress
directed the EPA to publish an additional EDSP list by October 30, 2010. The
Agency published EDSP List 2 in June 14, 2013. List 2 consisted of
109 chemicals—41 pesticides and 68 other chemicals that were identified
under the Safe Drinking Water Act amendments. Congress also directed the
EPA to issue 25 test orders per year from List 2, starting in fiscal year 2011. A
test order requires a pesticide manufacturer to conduct one or more specified
tests and submit the results to the EPA for review. As of this evaluation, the
Agency has not issued any test orders from List 2.
EDSP Tiers 1 and 2
The EPA uses a multistep process to determine a chemical's potential as an
endocrine disruptor. The EPA implemented a two-tiered approach as a result
21-E-0186
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of a recommendation from the Fjgure 2: EPA tiered testing process
Endocrine Disruptor Screening
and Testing Advisory
Committee. The purpose of the
Tier 1 screening is to identify
substances that have the
potential to interact with
estrogen, androgen, or thyroid
hormone systems. The purpose
of the Tier 2 testing is to
determine whether the
substance causes adverse
effects and to establish a
quantitative relationship
between the dose and the
adverse effect. Figure 2
illustrates the tiered testing
process.
EDSP Progress
After going through public
review and comment, the EPA
published a guidance document
titled Weight-of-Evidence:
Evaluating Results of EDSP
Tier 1 Screening to Identify the
Needfor Tier 2 Testing in 2011.
This WoE guidance document
sets forth general principles,
criteria, and considerations for evaluating data submitted as part of the EPA's
two-tiered paradigm for screening and testing chemicals for
endocrine-disrupting activity—that is, estrogen, androgen, and thyroid
hormonal systems. The EPA applied the WoE guidance to EDSP List 1-Tier 1
data in 2015 and made recommendations for Tier 2 testing. Table 1 describes
the prioritization of chemicals for tiered testing.
Chemical of potential concern
Tier 1 screening begins.
Tier 1 screening shows
chemical could potentially
be an endocrine disrupter.
Tier 2 testing begins.
Tier 1 screening shows
chemical is not an
endocrine disrupter. No
further action needed.
Endocrine disrupting
determination
Endocrine disrupter
Not an endocrine
disrupter
Source: OIG summary of the EPA's EDSP
information. (EPA OIG image)
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Table 1: Prioritization of chemicals for tiered testing

TIER 1
Identifies substances and chemicals
that may interact with the endocrine
system.
TIER 2
Determines whether a substance or chemical
adversely affects the endocrine system, if
warranted by the Tier 1 screening results.

LIST 1
The first group of 52 chemicals
identified for testing.
The EPA issued Tier 1 test
orders.
v/

The EPA recommended additional testing
known as Tier 2 testing, for 18 out of the
52 chemicals from List 1—Tier 1.
The EPA has not issued any Tier 2
test orders.
I,
X

LIST 2
The second group of 109 chemica
identified for testing.
The EPA has not issued any
Tier 1 test orders.
Is
X

The EPA has not identified nor issued
any Tier 2 test orders.
X

Source: OIG summary of EPA tier testing information. (EPA OIG table)
*As of this evaluation.
In 2015, the EPA published a Federal Register notice describing how the
Agency planned to incorporate an alternative scientific approach to screen
chemicals for their ability to interact with the endocrine system. The approach
would incorporate validated high-throughput assays and a computational
model and would serve as a faster, more cost-effective, and less
animal-intensive testing alternative for some of the assays in the EDSP Tier 1
battery.1
That same year, the EPA released the Tier 1 screening assay results for
52 pesticide chemicals. For each chemical, the EPA decided whether
additional Tier 2 testing was necessary based on whether the evidence from
the assay results, as well as other scientifically relevant data, showed potential
for endocrine activity. Based on its 2015 findings, the EPA recommended that
18 of the 52 chemicals undergo Tier 2 testing. In 2021, the OCSPP is still
evaluating whether these chemicals need Tier 2 wildlife testing to conduct the
chemical's ecological risk assessment. Wildlife testing are EDSP tests that the
EPA uses to characterize the endocrine-disruptor activity of the chemical and
to assess the chemical's risk to wildlife. The OCSPP has subsequently decided
that three of these chemicals no longer need Tier 2 human health studies for
the chemical's human health risk assessment. For the two chemicals that the
OCSPP decided still needed Tier 2 human health studies, the OCSPP has yet
1 High-throughput assays are automated methods that allow for a large number of chemicals to be rapidly evaluated
for a specific type of bioactivity at the molecular or cellular level.
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to receive the Tier 2 human health data from the chemicals' manufacturers.
Figure 3 describes a general timeline of EDSP progress.
Figure 3: Timeline on EDSP progress
— 1995-
1996-,
~ 1998
-2000-
2005-
r2005
1-2009
-2010
• EPA announces use of
cutting edge technology to
screen chemicals.
• EPA releases screening
results of endocrine disruptor
screening for 52 pesticide
chemicals.
• EPA finalizes EDSP Tier 2
test guidelines.
2014 *
2015*
2015-
-2020-
-#2021 -1
EPA has not provided EDSP
updates since 2015.
• Congress passes the FQPA
requiring EPA to create the
EDSP.
• EPA establishes the EDSP.
• EPA publishes a draft
WoE guidance document.
• EPA publishes draft
EDSP List 2.
• OiG issues a report on
EDSP.
EPA publishes final
approach for initial
screening.
Federal Insecticide,
Fungicide, and
Rodenticide Act SAP
review for Tier 1 results.
EPA issues Tier 1 (List 1
Screening Orders.
Source: OIG timeline based on the EPA's EDSP materials. (EPA OIG image)
Computational Toxicology
Computational toxicology is the application of mathematical and computer
models to help assess chemical hazards and risks to human health and the
environment. In 2012, the EDSP began a multiyear transition to use
computational toxicology methods and high-throughput screens to quickly and
cost-effectively assess potential chemical toxicity (Figure 4).
Figure 4: Tiered testing versus computational toxicology
Tiered Testing
• More expensive.
• Animal intensive.
Computational
Toxicology
• Faster test.
Cost effective.
Source: OIG summary of EPA information. (EPA OIG image)
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The initiative, referred to as EDSP21—or EDSP in the 21st century—aimed to
use computational or high-throughput screening assays to prioritize and screen
chemicals to determine their potential to interact with estrogen, androgen, or
thyroid bioactivity.
Internal Controls
Every federal program is required to have internal controls, and federal managers
are responsible for maintaining an effective internal control system. Internal
controls comprise the plans, policies, and procedures used to implement the
regular operation of the program, as well as to achieve the program's goals and
objectives. The U.S. Government Accountability Office's Standards for Internal
Control in the Federal Government, known as the Green Book,2 contains
standards to implement management control requirements, including program
operations, data collection and reporting, and consistent implementation. It also
notes that programs should use relevant data from reliable sources to support
decisions and federal managers should use performance measures to evaluate
performance in achieving objectives. The Green Book also states that information
should be communicated at all levels within and outside an organization.
Per the Government Accountability Office, to assist performance monitoring,
federal managers should promptly resolve the findings of audits and other reviews
and complete and document corrective actions to remediate internal control
deficiencies on a timely basis. The Office of Management and Budget's Circular
No. A-123, Management's Responsibility for Enterprise Risk Management and
Internal Control, issued on July 15, 2016, requires federal managers to implement
Government Accountability Office guidance and defines management's
responsibilities for assessing and managing programmatic risks.
EPA OIG's Prior Review of the Endocrine Disruptor Screening Program
The OIG evaluated the EDSP in Report No. ll-P-0215. EPA's Endocrine Disruptor Screening Program Should Establish
Management Controls to Ensure More Timely Results, issued May 3, 2011. The OIG sought to determine whether the
EPA had planned and conducted the requisite research and testing to evaluate and regulate endocrine-disrupting
chemicals.
The OIG concluded, in part, that the EDSP had not:
• Determined whether any chemical is an endocrine disruptor since the FQPA and Safe Drinking Water Act
amendments were passed.
• Developed a management plan laying out the program's goals and priorities or established outcome
performance measures to track program results.
• Conducted annual internal program reviews of the EDSP.
The OIG made six recommendations to strengthen the EDSP, including that the EPA finalize Tier 1 and Tier 2 criteria to
evaluate testing data, develop performance measures and a Comprehensive Management Plan, and hold annual
program reviews. The Agency agreed with the findings and conclusions and provided acceptable corrective actions.
2 U.S. Government Accountability Office, Standards for Internal Control in the Federal Government,
GAO-14-704G, September 10, 2014.
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Responsible Offices
The OCSPP is responsible for the issues in this report. Within the OCSPP, the
Office of Pesticide Programs oversees the EDSP.
Scope and Methodology
We conducted this evaluation from December 2020 to June 2021 in accordance
with the Quality Standards for Inspection and Evaluation, published in
January 2012 by the Council of the Inspectors General on Integrity and
Efficiency. Those standards require that we perform the evaluation to obtain
sufficient, competent, and relevant evidence to provide a reasonable basis for our
findings, conclusions, and recommendations based on our objectives. We believe
that the evidence obtained provides a reasonable basis for our findings,
conclusions, and recommendations.
We reviewed statutory and regulatory language, the EPA's strategic plan titled
Working Together: FY2018-2022 U.S. EPA Strategic Plan, relevant guidance,
and procedure documents. We also reviewed materials provided by the EDSP,
including the WoE guidance document; the EDSP's 2018 draft Comprehensive
Management Plan, or CMP; and other relevant internal documents. We
interviewed OCSPP staff and managers to gather their perspectives on the
program and its progress.
Results
Twenty-four years after passage of the FQPA and Safe Drinking Water Act
amendments in 1996, the EPA's EDSP has made limited progress in
implementing Section 408(p)(3)(A) of the FFDCA as amended by the FQPA,
which requires the EPA to test all pesticide chemicals for endocrine-disruption
activity. In addition, the OPP's Human Effects Division and Environmental Fate
and Effects Division recommended on June 29, 2015, that 17 of 18 pesticides
from List 1 needed additional EDSP Tier 2 testing for endocrine disruption in
wildlife in order to provide the data needed to conduct an ecological risk
assessment.3 However, the OPP management has not acted on that
recommendation.
EDSP testing delays are inconsistent with Section 408(p)(6) of the FFDCA, which
directs the EPA to take appropriate action to protect public health if a substance is
found, as a result of testing and evaluation, to have an effect on the human
endocrine system. We also found that previous OCSPP leadership did not ensure
continued implementation of corrective actions related to the OIG's 2011 report
recommendations. The EDSP has not had effective internal controls in place
since 2015.
3 The 18th pesticide needed only Tier 2 human health testing.
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Without the required testing, the EPA cannot make measurable progress toward
compliance with statutory requirements or safeguard human health and the
environment against risk from endocrine-disrupting chemicals. Without internal
controls, the EDSP cannot have reasonable assurance that the goals and objectives
of the program will be accomplished and that resources will be allocated
efficiently and effectively. Moreover, an established system of management
controls would provide mechanisms for consistent program operation.
Endocrine Disruptor Testing Has Stalled
The OCSPP has not implemented Section 408(p)(3) of the FFDCA to test all
pesticide chemicals for endocrine-disruption activity. In June 2015, the EPA
recommended that 18 pesticides from List 1 needed additional Tier 2 testing. As
of early 2021, the OCSPP has not issued any List 1-Tier 2 test orders for wildlife
studies and has only issued test orders for two pesticides for human health studies.
Likewise, although the EPA developed and published List 2 with 109 chemicals,
the EPA did not issue any List 2-Tier 1 test orders. As a result, the EPA has not
made meaningful progress in meeting its statutory obligation to test all pesticide
chemicals for endocrine-disruption activity.
We also found that the EPA did not meet a congressional direction from the fiscal
year 2010 House Appropriations Committee report to publish EDSP List 2 by
October 30, 2010. Instead, the EPA published List 2 on June 14, 2013, more than
two-and-a-half years after the deadline. Furthermore, Congress directed the EPA
to issue 25 test orders per year from List 2 starting in fiscal year 2011. As of
February 2021, the Agency still had not issued any List 2-Tier 1 test orders.
OPP staff and managers stated that a lack of overall support and direction for the
EDSP from previous OCSPP leadership resulted in no testing progress. We found
that previous OCSPP leaders did not make the necessary decisions to issue List 1-
Tier 2 and List 2-Tier 1 test orders. When asked why testing decisions were not
made, one EDSP staff person reported that previous leaders instructed them to
treat the EDSP as if the program had been eliminated from the EPA's budget even
though Congress funded the program.4 Without EDSP testing progress, the EPA
cannot adequately characterize or assess whether pesticides, chemicals, and other
environmental contaminants pose a endocrine-disruptor risk to estrogen,
androgen, and thyroid hormone systems.
Opportunity Exists to Incorporate EDSP Tier 1 Testing into Pesticide
Registration Application
The OCSPP's pace of testing pesticides for endocrine-disruption activity is
insufficient to keep up with the growth in pesticide registrations. Since the
EPA established the EDSP in 1998, the number of active pesticide
4 OIG Notification Memorandum, Performance Measures for Eliminated EPA Programs Later Funded by
Congressional Appropriation. Project No. OE-FY21-Q135. March 8, 2021.
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registrations has increased at a much faster pace than the EPA's pesticide
testing. Figure 5 depicts the increase in the number of pesticide registrations
from 1999 through 2020 and the number of EDSP Tier 1 test orders issued by
the EPA.
Figure 5: Approximate number of registered pesticides in 1999 and 2020
versus EDSP Tier 1 test orders
Source: OIG analysis of EPA information. (EPA OIG image)
In order to mitigate the ever-growing backlog, the EPA needs to consider
other processes to generate the necessary EDSP evaluation data. For example,
the OPP's pesticide registration program could incorporate EDSP testing as a
registration data requirement. Under 40 C.F.R. § 158, the EPA's pesticide
registration process has mandatory data requirements that are needed during
the application process. If the EDSP testing is a pesticide registration data
requirement, all new pesticide registration applications would include EDSP
Tier 1 data. Absent this, the EPA will continue to issue registrations for new
pesticides without obtaining additional information on the pesticides' potential
endocrine-disruptor activity.
EDSP Tier 2 Testing Delayed by Additional Evaluation of Tier 1 Data
We found that the OCSPP did not act in a timely manner on the 2015
recommendations from its own Health Effects Division and Environmental
Fate and Effects Division that 18 List 1 pesticides should undergo additional
Tier 2 testing. When the OCSPP conducted its 2015 evaluation of the List 1-
Tier 1 data, it followed its established 2011 WoE guidance. The
Environmental Fate and Effects Division recommended that the OCSPP
conduct 23 Tier 2 studies across 18 List 1 pesticides. As stated earlier, the
OCSPP is still evaluating whether these pesticides need Tier 2 wildlife testing
to conduct the pesticide's ecological risk assessment. The OCSPP has
subsequently decided that three of these pesticides no longer need Tier 2
human health studies for the pesticide's human health risk assessments. For
1,315 registered pesticides in 2020.
A 48 percent increase since 1999.
890 registered pesticides in 1999.
The number of registered pesticides when
the EDSP began.
52 EDSP Tier 1 test orders issued.
About 4 percent of the number of
registered pesticides in 2020.
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the two pesticides that the OCSPP decided still needed Tier 2 human health
studies, the OCSPP has yet to receive the Tier 2 human health data from the
manufacturers. Without EDSP Tier 2 data, the EPA cannot fully characterize
or assess whether these pesticides pose an endocrine-disruptor risk to the
estrogen, androgen, and thyroid hormone systems.
We found that previous OCSPP leadership decided to forgo the office's
established WoE approach for evaluating EDSP Tier 1 data and, instead,
undertook and reevaluated the List 1-Tier 1 data using a different approach.
Unlike the OCSPP's established WoE guidance, an EDSP manager stated that
the OCSPP's new approach has not yet undergone public review and
comment or been reviewed by the Federal Insecticide, Fungicide, and
Rodenticide Act Science Advisory Panel. As of June 2021, the OCSPP's
reevaluation of the List 1-Tier 1 data is still pending. In its draft reevaluation
of the List 1-Tier 1 data, the OCSPP proposed that no additional List 1-Tier 2
wildlife studies were needed. By not communicating this change in its
evaluation approach for EDSP Tier 1 data—and by continuing to delay this
reevaluation—the EPA risks public confidence in its commitment to test and
evaluate pesticides for endocrine-disruptor activity.
Changing Evaluation Approach After Receiving Data Can Lead to
Appearance of Bias
Since the OCSPP changed its evaluation approach after it received the Tier 1
data and after it recommended additional Tier 2 testing, the OCSPP's new
evaluation approach of the Tier 1 data can appear biased. The OIG's
2011 EDSP report recommended that the OCSPP "finalize specific criteria for
evaluating the Tier 1 screening data received." The OIG report stated that the
EPA needed to have this evaluation criteria in place before receiving the
Tier 1 data in order to avoid an appearance of bias. The OCSPP issued the
final WoE guidance in 2011 and implemented the EPA's WoE guidance in its
2015 recommendations. The OCSPP's decision to later reevaluate the same
List 1-Tier 1 data using a different set of evaluation criteria after it already
received the data could lead to an appearance of bias.
Potential bias also stems from the OCSPP not reevaluating all 52 pesticides'
List 1-Tier 1 data, but only evaluating List 1-Tier 1 data for the 17 pesticides
in which the EPA had previously recommended additional Tier 2 wildlife
testing in 2015. The OCSPP can appear biased by not using its new approach
to reevaluate the 35 pesticides for which no additional Tier 2 testing was
recommended. By not implementing the 2015 WoE recommendations for
additional Tier 2 testing, the EPA risks losing credibility with the public that
its decisions are impartial.
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EDSP Has Not Fully Implemented Effective Internal Controls
The EPA does not have internal controls in place to provide reasonable assurance
of effective program implementation of the EDSP. The EDSP has not finalized
strategic guidance documents or performance
measures on achieving its statutory requirements.
Additionally, the EDSP has not conducted any
internal program reviews to monitor or assess
progress in fulfilling the requirements of the
FFDCA, as amended by the FQPA. The OIG's
2011 report found that internal controls were
missing and recommended that, among other
actions, that the EPA develop a strategic planning
document known as the CMP, and annually review
EDSP results, progress toward milestones, and
achievement of performance measures. The EPA
agreed to corrective actions that address these recommendations, but we could not
confirm that the Agency conducted or implemented any of this work beyond an
initial period of compliance with them.
Internal controls help ensure accountability and enhance transparency of the steps
needed to implement a program and achieve results. Without internal controls, the
EDSP cannot have reasonable assurance that program goals and objectives will be
accomplished and that resources will be allocated efficiently and effectively.
Moreover, an established system of internal controls would provide mechanisms
for consistent program operations that would outlast changes in leadership and
increase programmatic progress.
EDSP Does Not Have Strategic Plan
The EDSP does not have a strategic or annual planning document that clarifies
priorities or guides the program's activities. In response to the OIG's
2011 report recommendations, the EDSP agreed to develop and publish a
CMP. The 2014 CMP provided strategic guidance and included estimates of
the EDSP's budget requirements, priorities, goals, and key activities. It also
discussed performance measures and annual review planning. However, the
OCSPP has not finalized and published a CMP since 2014. A draft 2018 CMP
was provided to OCSPP leadership in 2019, but it was never finalized. As a
result, the EDSP has not had strategic guidance since the 2014 CMP. As of
this evaluation, no other consistent or standardized system of planning for the
EDSP has been implemented.
The absence of a strategic plan also impacts the OCSPP's EDSP resource
allocations. In fiscal year 2021, the program was allocated $7.5 million but
had only approximately four full-time equivalent staff members, according to
OCSPP budget staff. OCSPP budget staff indicated that, based on the actual
Complying with key internal
control requirements concerning
risk assessment is a top
management challenge for the
Agency, as identified in OIG
Report No. 20-N-0231. EPA's FYs
2020-2021 Top Management
Challenges, issued July 21, 2020.
The EPA faces overarching
challenges in implementing and
operating internal controls that
establish and maintain an
effective work environment.
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budget allocation, the program could support at least seven full-time
equivalent staff members. Several staff and managers shared their belief that
the program is understaffed, which may impact the program's ability to make
measurable progress.
EDSP Does Not Have Performance Measures
The EDSP has not developed performance measures to determine the
effectiveness of the program. The Government Accountability Office's Green
Book states that management should evaluate performance in achieving
objectives. The 2011 OIG report recommended that the EDSP develop
short-term, intermediate, and long-term outcome performance measures and
additional output performance measures, with appropriate targets and time
frames, to measure program progress and results. In response, performance
measures were developed and included in the 2014 CMP. We found that, after
the 2014 CMP, the EDSP has not documented performance measures and has
not identified short-term, intermediate, and long-term targets to clarify
expectations and guide work prioritization. In fact, some program staff stated
that the program lacked support and some staff were specifically instructed to
function as if the program was not funded. Absent performance measures, the
EPA cannot appropriately track the EDSP's progress toward meeting statutory
requirements on identifying and testing endocrine-disrupting chemicals.
EDSP Has Not Conducted Internal Monitoring Reviews
The EDSP has not conducted any internal monitoring, such as annual reviews,
to determine whether the program is achieving its goals. Monitoring is an
important component of internal control and encompasses activities that
management establishes and operates to assess the quality of performance
over time and to promptly resolve the findings of audits and other reviews.
According to the Office of Management and Budget's Circular No. A-123,
continuous monitoring and other periodic assessments should provide the
basis for the Agency's annual assessment of and report on internal controls.
The EDSP agreed to conduct annual reviews in response to the OIG's 2011
report recommendations, but none of the staff and managers we interviewed
could produce any documents from previous annual reviews. Absent
management establishing program accountability through consistent
monitoring and annual reviews, the EDSP will not be able to establish an
effective screening and testing program.
EDSP Needs to Improve Communication with Stakeholders
The EDSP needs to improve its communication with both internal and
external stakeholders. The Government Accountability Office's Green Book
states that management should communicate both internally and externally to
maintain accountability and transparency. In Working Together: FY 2018-
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2022 U.S. EPA Strategic Plan, one of the Agency's strategic objectives is to
"increase transparency and public participation," which includes coordination
across the EPA's programs to ensure alignment of mutual efforts. The
strategic objective also included platforms to ensure that the public can
meaningfully participate in all of the EPA's work—including policy making,
regulatory development, outreach, education, and community engagement.
Additionally, EPA Administrator Michael Regan emphasized the importance
of transparency and earning public trust in an April 12, 2021 agency wide
email that stated that the "EPA will provide for the fullest possible public
participation in decision-making."
Internally, the EDSP lacks an effective procedure for coordinating with other
EPA program offices that are responsible for potential endocrine-disrupting
chemicals. For example, the Office of Water conducts Safe Drinking Water
Act-related work on endocrine disruptors, and the Office of Research and
Development oversees the EPA's overall research planning. EDSP
management expressed concern on how to better engage other program offices
since everyone is strained for resources. The OCSPP's October 2020
reorganization gives the EDSP an opportunity to develop needed procedures
for internal communication and coordination with other relevant program
offices.
Despite public interest in the health effects from endocrine-disrupting
chemicals, we found that the EDSP has not published any technical
documents for public review and comment since 2015. EDSP staff stated that
they have been working on a summary of the comments the EPA received for
its 2015 Federal Register notice regarding its plan to incorporate an
alternative scientific approach to screen potential endocrine-disrupting
chemicals and the Agency's responses to those comments. The EDSP still
needs to complete and publish its comment responses to the Federal Register
notice.
EDSP staff said that they are working on a white paper that summarizes the
scientific progress for using new approach methodologies for prioritizing and
screening chemicals. Staff added that the white paper lists which new
approach methodologies are considered as alternatives to some of the
11 assays in the Tier 1 screening battery and could be considered as "other
scientifically relevant information" toward fulfilling certain Tier 1 screening
requirements. In reviewing the EDSP's website, we found that most of the
website has not been updated since 2017. Absent transparent internal and
external communication regarding the EDSP, the public cannot make
necessary decisions on endocrine disruptors and their potential health effects.
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Conclusions
In 1996, Congress directed the EPA to establish the EDSP, and the program
received approximately $7.5 million in funding in fiscal year 2021. Yet, the EDSP
can show only limited results. Without the required testing and an effective
system of internal controls, the EPA cannot make measurable progress toward
compliance with statutory requirements or safeguard human health and the
environment against risk from endocrine-disrupting chemicals.
Recommendations
We recommend that the assistant administrator for Chemical Safety and Pollution
Prevention:
1. Issue Tier 1 test orders for each List 2 chemical or publish an explanation
for public comment on why Tier 1 data are no longer needed to
characterize a List 2 chemical's endocrine-disruption activity.
2. Determine whether the EPA should incorporate the Endocrine Disruptor
Screening Program Tier 1 tests (or approved new approach
methodologies) into the pesticide registration process as mandatory data
requirements under 40 C.F.R. § 158 for all pesticide use patterns.
3. Issue List 1-Tier 2 test orders for the 18 pesticides in which additional
Tier 2 testing was recommended or publish an explanation for public
comment on why Tier 2 data are no longer needed to characterize the
endocrine-disruption activity for each of these 18 pesticides.
4. Issue for public review and comment both the Environmental Fate and
Effects Division's approach for the reevaluation of List 1-Tier 1 data and
the revised List 1-Tier 2 wildlife recommendations.
5. Develop and implement an updated formal strategic planning document,
such as the Comprehensive Management Plan.
6. Develop performance measures, with reasonable time frames, to document
progress toward and achievement of milestones or targets. Specifically,
the Endocrine Disruptor Screening Program should consider at least one
performance measure that tracks progress in testing pesticides for human
endocrine disruptor activity.
7. Conduct annual internal program reviews of the Endocrine Disruptor
Screening Program.
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8. Complete and publish the Endocrine Disruptor Screening Program's
response(s) to 2015 Federal Register notice comments and its related
white paper.
9. Establish a procedure for Endocrine Disruptor Screening Program
communications and coordination with relevant Agency program offices
with testing responsibilities.
10. To increase external communication and transparency, update the
Endocrine Disruptor Screening Program website, including the program
timeline, and publish any relevant program documents.
Agency Response and OIG Assessment
The EPA generally agreed with our recommendations and provided acceptable
corrective actions and estimated completion dates for all ten recommendations.
The recommendations are considered resolved with corrective actions pending.
We also revised our report where appropriate based on technical comments
provided by the Agency.
The Agency's full response to our draft report is in Appendix A.
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Status of Recommendations and
Potential Monetary Benefits
RECOMMENDATIONS
Rec.
No.
No.
Subject
Status1
Action Official
15 Issue Tier 1 test orders for each List 2 chemical or publish an
explanation for public comment on why Tier 1 data are no longer
needed to characterize a List 2 chemical's endocrine-disruption
activity.
15 Determine whether the EPA should incorporate the Endocrine
Disruptor Screening Program Tier 1 tests (or approved new
approach methodologies) into the pesticide registration process
as mandatory data requirements under 40 C.F.R. § 158 for all
pesticide use patterns.
15 Issue List 1—Tier 2 test orders for the 18 pesticides in which
additional Tier 2 testing was recommended or publish an
explanation for public comment on why Tier 2 data are no longer
needed to characterize the endocrine-disruption activity for each
of these 18 pesticides.
15 Issue for public review and comment both the Environmental
Fate and Effects Division's approach for the reevaluation of
List 1—Tier 1 data and the revised List 1—Tier 2 wildlife
recommendations.
Planned
Completion
Date
Potential
Monetary
Benefits
(in $000s)
Assistant Administrator for 9/30/25
Chemical Safety and
Pollution Prevention
Assistant Administrator for 9/30/24
Chemical Safety and
Pollution Prevention
Assistant Administrator for 9/30/24
Chemical Safety and
Pollution Prevention
Assistant Administrator for 12/31123
Chemical Safety and
Pollution Prevention
15 Develop and implement an updated formal strategic planning
document, such as the Comprehensive Management Plan.
Assistant Administrator for
Chemical Safety and
Pollution Prevention
9/30/22
15 Develop performance measures, with reasonable time frames, to
document progress toward and achievement of milestones or
targets. Specifically, the Endocrine Disruptor Screening Program
should consider at least one performance measure that tracks
progress in testing pesticides for human endocrine disruptor
activity.
15 Conduct annual internal program reviews of the Endocrine
Disruptor Screening Program.
Assistant Administrator for 10/1 /24
Chemical Safety and
Pollution Prevention
Assistant Administrator for 9/30/22
Chemical Safety and
Pollution Prevention
10
16 Complete and publish the Endocrine Disruptor Screening
Program's response(s) to 2015 Federal Register notice
comments and its related white paper.
16 Establish a procedure for Endocrine Disruptor Screening
Program communications and coordination with relevant Agency
program offices with testing responsibilities.
16 To increase external communication and transparency, update
the Endocrine Disruptor Screening Program website, including
the program timeline, and publish any relevant program
documents.
Assistant Administrator for 12/31/21
Chemical Safety and
Pollution Prevention
Assistant Administrator for 9/30/21
Chemical Safety and
Pollution Prevention
Assistant Administrator for 12/30/21
Chemical Safety and
Pollution Prevention
1 C = Corrective action completed.
R = Recommendation resolved with corrective action pending.
U = Recommendation unresolved with resolution efforts in progress.
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Appendix A
Agency Response to Draft Report

% PR0^0
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2. Compliance with Section 408(p)(6) of the Food Quality Protection Act, which requires
the EPA to take action when finding, through testing and evaluation, that a substance has
an endocrine effect on humans.
OCSPP is in general agreement with the 10 recommendations in the Draft Report regarding the
Endocrine Disruptor Screening Program (EDSP). OCSPP is proposing to broadly address the
recommendations with an iterative EDSP Strategic Plan, which we anticipate will be developed
and updated to reflect new data and findings. This EDSP Strategic Plan is described in more
detail in our response to the specific recommendations, below.
As an important first step, OCSPP has already put into place a new organizational structure to
ensure management accountability for the EDSP. With the OCSPP reorganization in October
2020, the Office of Pesticide Programs (OPP) now has responsibility for the EDSP, which was
previously effectively divided between OPP and the former Office of Science Coordination and
Policy (OSCP). OPP has already begun the process of aligning the human and technical
infrastructure to accelerate the implementation of EDSP testing and decisions. OCSPP is
optimistic that through these efforts, the pace of evaluations for endocrine disruption will
accelerate, become more transparent, and be more clearly communicated.
While OCSPP acknowledges the challenges faced by the EDSP in the past, including efforts
from previous OCSPP leadership to not fully implement the EDSP and its funding, OCSPP
disagrees with the Draft Report's finding that the Agency "has not made meaningful progress in
meeting its statutory obligation to test all pesticides for endocrine-disruption activity." By
developing and enacting a screening and testing program, EPA has fulfilled numerous goals
associated with the legal mandate. Notably, test orders were issued for Tier 1 data for 67 List 1
chemicals in 2009, and reviews of the submitted data and conclusions were published in 2015.
Furthermore, in addition to the Tier 1 data on the List 1 chemicals, EPA has:
• Generated in vitro estrogen and androgen receptor pathway data for approximately 500
pesticide chemicals;
• Compiled some human health Tier 2 data for hundreds of conventional, food-use
pesticides;
• Identified EDSP assays from the scientific literature on a wide range of EDSP chemicals
for the uterotrophic, Hershberger, steroidogenesis, amphibian metamorphosis, male and
female pubertal assays;
• Developed cancer and/or non-cancer human health risk assessments using endocrine
related endpoints for over 100 conventional pesticides; and
• Initiated collaborative work with the Office of Research and Development (ORD) to
collect additional in vitro data on estrogen and androgen for approximately 250-750
additional pesticide active ingredients.
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In assessing the EDSP's accomplishments, it is important to note that in the last decade, EPA
focused its efforts on developing new approach methods (NAMs).5 This investment was made
because of the extensive resources (time, cost, and use of laboratory animals) required to
develop and evaluate the Tier 1 -List 1 data. These new approach methods are faster, more
efficient, and provide more human-relevant and mechanistically-driven data for use in the
evaluation of estrogen, androgen, and thyroid bioactivity. In collaboration with ORD and the
National Institutes of Environmental Health Science (NIEHS) - NTP Interagency Center for the
Evaluation of Alternative Toxicology Methods (NICEATM), the EDSP has made substantial
progress in this area. OCSPP's announcement of the acceptance and use of in vitro and
computational approaches will be described in a NAMs White Paper, which will be published
for public comment in 2021, and is expected to be finalized in 2022.
OPP leadership met with me on June 22, 2021 to discuss their vision for an EDSP transition. As
part of this vision, an internal council of staff across OPP will be created to address the science
policy issues associated with the EDSP data needs. This OPP/EDSP Council will begin meeting
in September 2021. One of its first duties will be to develop 3-6 case studies for the different
types of pesticide chemicals (e.g., conventional, antimicrobial, biopesticides, etc) regulated by
OCSPP. These case studies will evaluate the approaches for using NAM data, in combination
with existing Tier 1 or Tier 2 studies submitted for pesticide registration in the 40 CFR part 158
and other scientifically relevant information. The evaluations of these case studies will be used
to inform short, intermediate, and long-term activities for the EDSP, including the development
of the ESDP Strategic Plan, additional research needed by ORD or NIEHS, and possible test
order needs.
Even with the expected efficiencies from this approach, prioritization of the workload is critical
because of the large number of substances identified as being within the EDSP universe. EPA's
first priority will be on the statutorily-required testing of pesticide chemicals (i.e., active
ingredients and inerts). This work will occur prior to the evaluation of the discretionary Safe
Drinking Water Act (SDWA) chemicals. Moreover, the ordering (i.e., prioritization) of chemical
testing for EDSP is currently being reevaluated to better align with pesticide registration review
and registration schedules. Accordingly, while the Draft Report in some cases recommends a
binary choice of actions, OCSPP's proposed Corrective Action Plan in some instances explains
why it is necessary to propose additional, alternative corrective actions to address the
recommendations.
In addition to this memo, OCSPP has prepared Technical Comments on the Draft Report, which
we will transmit under separate cover. These Technical Comments in redline/strikeout (1)
corrections, (2) proposed language changes and (3) lesser issues of concern in the Draft Report
itself.
II. OCSPP's Response to the Recommendations:
5 NAMs refer to any technology, methodology, approach, or combination that can provide information on chemical
hazard and risk assessment to avoid the use of animal testing.
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Recommendation 1: Issue Tier 1 test orders for each List 2 chemical or publish an explanation
for public comment on why Tier 1 data is no longer needed to characterize a List 2 chemical's
endocrine-disruption activity.
OCSPP acknowledges that Tier 1 test orders have not been issued for List 2 chemicals and
agrees that action on List 2 is needed. OCSPP agrees with two possible outcomes that the OIG
proposes: that List 2 test orders need to be issued, or that an explanation should be published
articulating why test orders are not needed for List 2 (including that EPA expects to acquire the
needed data from other sources). OCSPP proposes, as an additional action, that some decisions
on some List 2 chemicals may be delayed due to test chemical reprioritization consistent with the
needed refocus to address mandatory elements under the statute first, namely estrogen effects on
pesticide chemicals.
• Proposed Corrective Action la: OCSPP, with input from the Office of Research and
Development and the Office of Water, will publish for comment a List 2 Action Plan,
which may include a combination of test orders, explanations as to why test orders are
not needed, or a reprioritization of the order of EDSP evaluations.
• Proposed Corrective Action lb: Following notice and comment as described in
Corrective Action la, OCSPP will initiate the process to issue test orders for List 2
substances, as appropriate.
• Target Completion Dates: September 30, 2024 for Action la. September 30, 2025 for
lb.
Recommendation 2: Determine whether the EPA should incorporate the EDSP Tier 1 tests (or
approved new approach methodologies) into the pesticide registration process as mandatory data
requirements under 40 C.F.R. § 158 for all pesticide use patterns.
OCSPP agrees that a determination should be made and shared with the public on whether the
EPA will incorporate the EDSP Tier 1 tests (or appropriate NAMs/new approach methodologies)
into the pesticide registration process as mandatory data requirements under 40 C.F.R. part 158
for all pesticide use patterns. OCSPP is not developing new EDSP test guidelines for NAMs, but
instead is accepting NAMs as other scientifically relevant information for alternatives to Tier 1
guideline studies on a case-by-case basis.
• Proposed Corrective Action 2: OCSPP will make a determination on the inclusion of
the EDSP Tier 1 tests into the pesticide registration process as mandatory data
requirement under 40 C.F.R. part 158 for all pesticide use patterns.
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• Target Completion Date: September 30, 2024.
Recommendation 3: Issue List 1-Tier 2 test orders for the 18 pesticides in which additional
Tier 2 testing was recommended or publish an explanation for public comment why this Tier 2
data is no longer needed to characterize the endocrine-disruption activity for each of these 18
pesticides.
OCSPP agrees the List 1-Tier 2 test orders for the 18 pesticides need to be addressed.
Recommendation 4, below, specifically addresses the List 1-Tier 2 ecotoxicology data needs for
17 pesticides. One of the 18 pesticides (Chlorthal Dimethyl (DCPA)), was not recommended for
any Tier 2 ecotoxicology data.
• Proposed Corrective Action 3a: OCSPP will make a determination on the need for List
1-Tier 2 data. OCSPP will also provide an explanation, which will be published for
public comment, for any of the 18 pesticides for which it is determined that Tier 2 data
is no longer needed.
• Proposed Corrective Action 3b: Following publication and comment as described in
Corrective Action 3a, OCSPP will initiate the process to issue any Tier 2 test orders for
List 1 determined to be needed.
• Target Completion Date: December 31, 2023 for Corrective Action 3a. September 30,
2024 for Corrective Action 3b.
Recommendation 4: Issue for public review and comment both the Environmental Fate and
Effects Division's approach for the reevaluation of List 1-Tier 1 data and the revised List 1-Tier
2 wildlife recommendations.
Along with Recommendation 3, OCSPP agrees that any revisions to the final determinations on
the List 1-Tier 1 data and any revisions to the List 1-Tier 2 wildlife recommendations need to be
issued for public review and comment.
• Proposed Corrective Action 4: OCSPP will issue for public review and comment any
reevaluation of List 1-Tier 1 data and any revisions to the List 1-Tier 2 wildlife
recommendations.
• Target Completion Date: Final determinations of the need for List 1-Tier 2
ecotoxicology data will be completed and posted for public comment by December 31,
2023 together with Proposed Corrective Action 3a.
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Recommendation 5: Develop and implement an updated formal strategic planning document,
such as the Comprehensive Management Plan.
OCSPP agrees with the finding that an updated formal strategic planning document should be
developed. At the same time, the previous Comprehensive Management Plan took significant
time and resources to develop, and such a model will not suit OCSPP's immediate needs.
Nevertheless, OCSPP is proposing to develop its EDSP Strategic Plan, which will be an iterative
document and will take into account the OCSPP re-organization and the EDSP's transition to a
focus on implementation.
• Proposed Corrective Action 5: OCSPP, with input from the Office of Research and
Development and the Office of Water, will develop an EDSP Strategic Plan. OCSPP
expects to update this document on an as needed basis.
• Target Completion Date: September 30, 2022.
Recommendation 6: Develop performance measures, with reasonable time frames, to document
progress toward and achievement of milestones or targets. Specifically, the Endocrine Disruptor
Screening Program should consider at least one performance measure that tracks progress in
testing pesticides for human endocrine disruptor activity.
OCSPP agrees that tracking the progress of the EDSP is an important component of the
reorganization and that at least one performance measure is needed. Testing and experimentation
can take months to years to develop, analyze and finalize conclusions on the data. Although
OCSPP has already taken steps to initiate some in vitro testing in collaboration with ORD, a
performance measure on testing pesticides for human endocrine disruptor activity cannot be
implemented immediately. This activity will incorporate an evaluation of whether testing is
needed.
• Proposed Corrective Action 6a: OCSPP will develop short-term performance measures,
such as scientific publications, number/type of accepted new approach methods, and
exemptions granted.
• Proposed Corrective Action 6b: OCSPP will develop longer-term performance
measures, including at least one measure to track progress in testing pesticides for human
endocrine disruptor activity.
• Target Completion Date: Short-term performance measures under Proposed
Corrective Action 6a will be developed by and tracked beginning October 1, 2022.
Long-term performance measures under Proposed Corrective Action 6b including at
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least one that tracks progress in the evaluation and testing of pesticides for human
endocrine disruptor activity will be developed and tracked by October 1, 2024.
Recommendation 7: Conduct annual internal program reviews of the Endocrine Disruptor
Screening Program.
OCSPP agrees that annual internal program reviews of the EDSP need to be conducted. This
review process will be conducted internally, within OCSPP, and will be designed to ensure that
proper management controls are in place so that progress and accountability within the EDSP
can be determined.
• Proposed Corrective Action 7a: OCSPP will conduct the first annual internal program
review of the EDSP, and provide a briefing and report out to the OCSPP Assistant
Administrator on EDSP progress, especially as it relates to the Corrective Actions in this
Report and progress developing the EDSP Strategic Plan.
• Target Completion Date: September 30, 2022.
Recommendation 8: Complete and publish the Endocrine Disruptor Screening Program's
response(s) to 2015 Federal Register notice comments and its related white paper.
OCSPP agrees that the Endocrine Disruptor Screening Program's response to the 2015 Federal
Register notice comments and the related NAM White Paper need to be completed and
published.
• Proposed Corrective Action 8: OCSPP will complete and publish the response to 2015
Federal Register notice comments and the NAM White Paper.
• Target Completion Date: OCSPP will complete and publish these documents by
December 2021.
Recommendation 9: Establish a procedure for Endocrine Disruptor Screening Program
communications and coordination with relevant Agency program offices with testing
responsibilities.
OCSPP agrees that a procedure for better communications and coordination between the
Endocrine Disruptor Screening Program and other Agency program offices needs to be
established. OCSPP already routinely coordinates with ORD and has already been including
EDSP in those discussions.
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• Proposed Corrective Action 9: OCSPP will establish a procedure for
communications and coordination with relevant Agency program offices with
EDSP testing responsibilities.
• Target Completion Date: OCSPP will establish the procedure by September 30, 2021.
Recommendation 10: To increase external communication and transparency, update the
Endocrine Disruptor Screening Program website, including the program timeline, and publish
any relevant program documents.
OCSPP agrees that the EDSP website needs updating.
• Proposed Corrective Action 10: The EDSP will update the EDSP website to post the
response to the 2015 Federal Register notice comments and the NAM White Paper on the
Endocrine Disruptor Screening Program website. Continuing updates, for example on the
OCSPP reorganization, will also be done as needed to increase external communication
and transparency.
• Target Completion Date: Corrections to the EDSP website, including hyperlinks to
documents and other webpages, have already begun. The NAM White Paper and
associated documents will be published on the Endocrine Disruptor Screening Program
website by December 30, 2021.
cc: All OCSPP DAAs
Program Office OD, DOD
Erin Barnes-Weaver, OIG
Lauretta Joseph, OIG
Michael Wilson, OIG
Natasha Henry, OIG
Janet L. Weiner, OCSPP Audit Liaison
Cameo Smoot, OPS Program Office Audit Liaison
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Appendix B
Distribution
The Administrator
Deputy Administrator
Chief of Staff, Office of the Administrator
Deputy Chief of Staff, Office of the Administrator
Assistant Administrator for Chemical Safety and Pollution Prevention
Agency Follow-Up Official (the CFO)
Agency Follow-Up Coordinator
General Counsel
Associate Administrator for Congressional and Intergovernmental Relations
Associate Administrator for Public Affairs
Deputy Assistant Administrator for Chemical Safety and Pollution Prevention
Director, Office of Pesticide Programs, Office of Chemical Safety and Pollution Prevention
Director, Office of Continuous Improvement, Office of the Chief Financial Officer
Audit Follow-Up Coordinator, Office of the Administrator
Senior Audit Advisor, Office of Chemical Safety and Pollution Prevention
Audit Liaison, Office of Pesticide Programs, Office of Chemical Safety and Pollution Prevention
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