Environmental Defense Fund v. Wheeler

CourtDistrict Court, District of Columbia
DecidedAugust 20, 2024
DocketCivil Action No. 2020-0762
StatusPublished

This text of Environmental Defense Fund v. Wheeler (Environmental Defense Fund v. Wheeler) is published on Counsel Stack Legal Research, covering District Court, District of Columbia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Environmental Defense Fund v. Wheeler, (D.D.C. 2024).

Opinion

UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLUMBIA

ENVIRONMENTAL DEFENSE FUND, et al.,

Plaintiffs, Civil Action No. 20-762 (LLA) v.

MICHAEL S. REGAN, et al.,

Defendants.

MEMORANDUM OPINION AND ORDER

Plaintiffs, five environmental organizations, sue the U.S. Environmental Protection

Agency (“EPA”) and EPA Administrator Michael S. Regan to enforce the transparency and

disclosure requirements of the Toxic Substances Control Act (“TSCA”), 15 U.S.C. § 2601 et seq.

The EPA moves for judgment on the pleadings, ECF No. 48, and Plaintiffs move to compel the

administrative record, ECF No. 45. For the reasons explained below, the court will DENY the

EPA’s motion for judgment on the pleadings and GRANT Plaintiffs’ motion to compel the

administrative record.

I. The Toxic Substances Control Act

“Congress enacted TSCA in 1976 with the express purpose of limiting the public health

and environmental risks associated with exposure to . . . toxic chemical substances.” Physicians

Comm. For Responsible Med. v. Johnson, 436 F.3d 326, 327 (2d Cir. 2006); see Trumpeter Swan

Soc’y v. Env’t Prot. Agency, 774 F.3d 1037, 1039 (D.C. Cir. 2014). The TSCA requires the EPA

to approve any new chemical before it can be manufactured. See generally 15 U.S.C. § 2604.

Manufacturers submit a notice for the EPA’s review which includes information about how the chemical could impact health or the environment. See id. § 2604(d)(1)(B), (C).1 That notice is

known as a “premanufacture notice” (“PMN”). See ECF No. 16 ¶ 21. The EPA is required to

inform the public within five business days of receiving a PMN application by publishing a “notice

of receipt” in the Federal Register. 15 U.S.C. § 2604(d)(2). The notice must identify the chemical,

list the uses of the chemical, and describe the nature and results of certain tests performed on the

chemical. Id.

The EPA must make a decision (a “risk determination”) on a PMN application within

ninety days of receipt, but it can extend by an additional ninety days for good cause. Id. § 2604(a),

(c), (i)(3). If the EPA finds that the proposed chemical “is not likely to present an unreasonable

risk of injury to health or the environment,” then the applicant may begin manufacturing the

chemical without restrictions. Id. § 2604(a)(3)(C). Otherwise, the EPA must impose protective

restrictions on manufacture and/or use. Id. § 2604(a)(3)(A) to (B), (e) to (f).

The TSCA requires the EPA to disclose all non-confidential information in the PMN

application to any interested person, id. § 2604(d)(1), by (1) placing “[a]ll information submitted

with a [PMN], including any health and safety study and other supporting documentation” in a

“public file for that [PMN],” 40 C.F.R. § 720.95; and (2) making the public file available, both via

request from the EPA Docket Center and by placing it online in an electronic docket for the PMN

at http://www.regulations.gov, id.; id. § 700.17(b)(1), (2).

1 A PMN must include “any information . . . related to the effect of any manufacture, processing, distribution in commerce, use, or disposal of such substance or any article containing such substance, or of any combination of such activities, on health or the environment” and “a description of any other information concerning the environmental and health effects of such substance, insofar as known to the [applicant] or insofar as reasonably ascertainable.” 15 U.S.C. § 2604(d)(1)(B), (C).

2 Manufacturers can assert that certain information is confidential and should not be

disclosed. See generally 15 U.S.C. § 2613. The manufacturer must substantiate its confidentiality

claim by showing that it has (among other things) “taken reasonable measures to protect the

confidentiality of the information” and “determined that the information is not required to be

disclosed or otherwise made available to the public under any other Federal law”—and that there

is “a reasonable basis to conclude that disclosure of the information is likely to cause substantial

harm to the competitive position of the [applicant].” Id. § 2613(c)(B). In addition to meeting these

requirements, the information must also qualify as a trade secret or privileged and confidential

information under the Freedom of Information Act (“FOIA”), 5 U.S.C. § 552, to be considered

confidential for TSCA purposes. 15 U.S.C. § 2613(a).

However, “any health and safety study” and “any information . . . from a health and safety

study” submitted with a PMN are not treated as confidential, even if they would otherwise meet

the statute’s confidentiality requirements. Id. § 2613(b)(2)(A)(ii), (B). This does not include

information from a study that “discloses processes used in the manufacturing or processing of a

chemical substance,” id. § 2613(b)(2), although “general description[s]” of such processes are not

protected, id. § 2613(b)(3)(B).

A manufacturer can also apply to manufacture the chemical for “test marketing purposes”

(the “test marketing exception” or “TME”). Id. § 2604(h)(1). “Immediately upon receipt of [a

TME] application,” the EPA “shall publish in the Federal Register notice of the receipt of such

application” and “shall give interested persons an opportunity to comment upon any such

application.” Id. § 2604(h)(6). The EPA must, “within 45 days of its receipt, either approve or

deny the application.” Id.

3 II. Plaintiffs’ Claims

Plaintiffs are five environmental organizations: Environmental Defense Fund, Center for

Environmental Health, Environmental Health Strategy Center, Natural Resources Defense

Council, and the Sierra Club. ECF No. 16 ¶¶ 14-18. They allege that the EPA has repeatedly

failed to comply with the TSCA’s disclosure requirements. See generally ECF No. 16. Their

claims fall into three categories, see ECF No. 22:

Insufficient Notice Claims (Counts I-III). The EPA violated the TSCA by not complying

with requirements (1) to publish notice of the receipt of PMN and TME applications in the Federal

Register by the statutory deadline, and (2) to include required information in the notices. ECF

No. 16 ¶¶ 144-66; see id. ¶¶ 86-96. Take, for example, one PMN designated “P-14-0314.” Id.

at 60 (Table 1). The EPA received the PMN on February 7, 2014, and was statutorily required to

post notice of that receipt within five business days, 15 U.S.C. § 2604(d)(2)—by February 17,

2014. ECF No. 16, at 60 (Table 1). Instead, the EPA posted notice of receipt on September 16,

2014—211 days late. Id. In fact, in at least thirty-five cases, the EPA published notice of receipt

after it had approved the chemical in question. Id.

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