American Crop Protection Ass'n v. U.S. Environmental Protection Agency

182 F. Supp. 2d 89, 32 Envtl. L. Rep. (Envtl. Law Inst.) 20442, 54 ERC (BNA) 1059, 2002 U.S. Dist. LEXIS 1713
CourtDistrict Court, District of Columbia
DecidedJanuary 31, 2002
DocketCIV.A.00-0811
StatusPublished
Cited by2 cases

This text of 182 F. Supp. 2d 89 (American Crop Protection Ass'n v. U.S. Environmental Protection Agency) 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
American Crop Protection Ass'n v. U.S. Environmental Protection Agency, 182 F. Supp. 2d 89, 32 Envtl. L. Rep. (Envtl. Law Inst.) 20442, 54 ERC (BNA) 1059, 2002 U.S. Dist. LEXIS 1713 (D.D.C. 2002).

Opinion

MEMORANDUM

ROBERTSON, District Judge.

Section 6(a)(2) of the Federal Insecticide, Fungicide, and Rodenticide Act (FI-FRA), 7 U.S.C. § 136 et seq., requires that pesticide registrants report to the Environmental Protection Agency (EPA) on an ongoing basis “factual information regarding unreasonable adverse effects on the environment of [a] pesticide.” FIFRA § 6(a)(2), 7 U.S.C. § 136d(a)(2). EPA interprets that directive to cover opinions regarding unreasonable adverse effects rendered by a registrant’s employees or agents, and it has issued a regulation to that effect. 40 C.F.R. § 159.158(a). In this suit, the American Crop Protection Association and others challenge that regulation on two grounds: first, that requiring opinions to be reported is beyond the authority Congress gave the EPA to require the reporting of “factual information”; and, second, that to the extent the regulation requires registrants to report *90 the opinions of non-testifying expert witnesses prepared in preparation of litigation, or of lawyers, it “undermines the availability of the work product doctrine and the attorney-client privilege to pesticide registrants,” PI. Mem. at 2, and is thus an unreasonable interpretation of the statute and contrary to law. I find, for the reasons set forth below, that EPA did not exceed its authority and that its interpretation of the statute is entitled to deference and reasonable. The order that accompanies this opinion accordingly denies plaintiffs’ motion for summary judgment and grants the government’s cross-motion — except to the extent that that motion seeks an advance blanket ruling on lawyer-client privilege and attorney work product. No ruling is made on that issue, because this record presents no concrete claim of privilege or of work product protection.

Background

A pesticide must be registered before being placed on the market. It will be registered only if EPA finds that it will “perform its intended function without unreasonable adverse effects on the environment.” 7 U.S.C. § 136a(c)(5)(C). Registration is not the end of the regulatory process: a pesticide registration may be maintained only if it does not “generally cause[ ] unreasonable adverse effects on the environment.” 7 U.S.C. § 136d(b). Congress gave the EPA authority to call for additional data as needed for the ongoing evaluation of pesticides. “If the Administrator determines that additional data are required to maintain in effect an existing registration of a pesticide, the Administrator shall notify existing registrants.” The authority to call for more data has teeth: if a registrant fails to provide information requested about a pesticide, EPA must issue a notice of intent to suspend the pesticide’s registration. 7 U.S.C. § 136a(c)(2)(B). The statute also imposes upon registrants a duty of self-reporting. If “at any time after the registration of a pesticide the registrant has additional factual information regarding unreasonable adverse effects on the environment of the pesticide, the registrant shall submit such information to the Administrator.” FI-FRA § 6(a)(2), 7 U.S.C. § 136d(a)(2). It is that requirement which gives rise to the dispute presented in this case.

The dispute between pesticide manufacturers and the EPA about reporting has been going on for more than twenty-six years. 1 EPA’s first regulation under section 6(a)(2) required registrants to report any information about adverse effects, 40 Fed.Reg. 28242, 28277 (July 3, 1975). EPA revoked that regulation in 1978, after concluding in response to an industry challenge that it “inadequately expresse[d] the agency’s interpretation of the requirements imposed by FIFRA Section 6(a)(2).” 43 Fed.Reg. 37610 (Aug. 23, 1978). EPA then issued an “interpretive memorandum” setting forth its view that the statute required registrants to report opinions, including expert opinions, as to the risks or benefits of registered pesticides. An industry challenge to that memorandum was dismissed for lack of standing, upon a finding that the memorandum had no legal effect, Chemical Specialties Mfrs. Ass’n v. United States EPA, 484 F.Supp. 513, 519 (D.D.C.1980)(Robinson, J.). The judge nevertheless volunteered his view that a requirement to report expert opinions would exceed EPA’s authority: “If Congress had intended to give § 6(a)(2) such broad scope, it would not have limited the information required to facts.” Id. at 518.

*91 EPA tried again in 1985. This time it issued a proposed interpretive rule and statement of policy that required the reporting of expert opinions. The preamble to this rule stated that “EPA and the Department of Justice believe that EPA is free to take the position that expert opinion evidence ... [is] covered by Section 6(a)(2) despite the dicta in CSMA, and EPA continues to take this position.” 50 Fed.Reg. 38115, 38116 (Sept. 20, 1985). After receiving comments, however, the agency decided not to make the rule effective after all, stating that “clarification of the rule was appropriate.” 57 Fed.Reg. 44290-91 (Sept. 24,1992).

Finally, EPA resorted to formal notice and comment rulemaking. The present rules implementing FIFRA section 6(a)(2) are the result of that process. 40 C.F.R. Part 159, 62 Fed.Reg. 49370 (Sept. 19, 1997). Since them effective date in August 1998, they have required that a registrant report information, possessed or received, that is “relevant to the assessment of the risks or benefits” of pesticide registrations, if the information falls within any of seven enumerated categories, 40 C.F.R. § 159.158(a), 2 or if the registrant “knows or reasonably should know” that the information might raise “concerns” with the EPA about the continued registration of the product. 40 C.F.R. § 159.195. The information that must be reported includes “conclusion(s) or opinion(s) rendered by a person who meets any of the following: (1) Who was employed or retained (directly or indirectly) by the registrant, and was likely to receive such information. (2) From whom the registrant requested the opinion(s) or eonclusion(s) in question. (3) Who is a qualified expert as described in § 159.153(b).” 3 40 C.F.R. § 159

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Bluebook (online)
182 F. Supp. 2d 89, 32 Envtl. L. Rep. (Envtl. Law Inst.) 20442, 54 ERC (BNA) 1059, 2002 U.S. Dist. LEXIS 1713, Counsel Stack Legal Research, https://law.counselstack.com/opinion/american-crop-protection-assn-v-us-environmental-protection-agency-dcd-2002.