Rise for Animals v. Vilsack

CourtDistrict Court, D. Maryland
DecidedMarch 21, 2024
Docket8:22-cv-00810
StatusUnknown

This text of Rise for Animals v. Vilsack (Rise for Animals v. Vilsack) is published on Counsel Stack Legal Research, covering District Court, D. Maryland primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Rise for Animals v. Vilsack, (D. Md. 2024).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF MARYLAND

RISE FOR ANIMALS, et al., *

Plaintiffs, *

v. * Case No. 8:22-cv-00810-JRR TOM VILSACK, Secretary of the United * States Department of Agriculture, et al., * Defendants. *

* * * * * * * * * * * * *

MEMORANDUM OPINION I. INTRODUCTION Plaintiffs Rise for Animals (“Rise”) and Animal Legal Defense Fund (“ALDF”) are nonprofit organizations focused on advancing the interests of animals. (ECF No. 1 ¶¶ 6, 12.) Specifically, Rise seeks to end the suffering of nonhuman primates used in research, and works to educate the public, lawmakers, and others to that end. Id. ¶ 6. Similarly, ALDF engages in campaigns to bring public awareness to what it views as the failures of laboratories to provide proper care for their research subject primates. Id. ¶ 12. Rise and ALDF bring this action pursuant to the Administrative Procedure Act (“APA”) against Defendants Tom Vilsack, Secretary of the United States Department of Agriculture (“USDA”), and Elizabeth Goldentyer, Acting Deputy Administrator for Animal Care at the Animal Plant and Health Inspection Service (“APHIS”).1 Plaintiffs seek judicial review of the Agency’s policy (“Partial Inspection Policy”)2 under which, in Plaintiffs’ view, the Agency “relies

1 The USDA is the parent agency of APHIS. The USDA and APHIS are together referred to herein as the “Agency.” 2 Throughout the Complaint and the parties’ motions papers, reference is made to the “Partial Inspection Policy,” the “Policy,” the “unlawful Policy,” the “Inspection Policy,” and the “Focused Inspection” seemingly interchangeably. on third-party accreditation by the Association of the Assessment and Accreditation of Laboratory Animal Care (“AAALAC”), a private trade association, to evade its statutory obligation to conduct full annual inspections of research facilitates as required under the Animal Welfare Act (“AWA”), 7 U.S.C. § 2146.” (ECF No. 1 at 1.) 3

Pending before the court are Plaintiffs’ Motion for Summary Judgment and memorandum of law in support thereof (ECF Nos. 25 and 25-1) and Defendants’ Motion to Dismiss and Cross- Motion for Summary Judgment and memorandum of law in support thereof. (ECF Nos. 35 and 35-1.) The court has reviewed the parties’ submissions and no hearing is necessary. Local Rule 105.6 (D. Md. 2023). II. BACKGROUND A. Statutory and Regulatory Background 1. Animal Welfare Act of 1966 In 1966, Congress enacted the AWA to “[e]nsure that animals intended for use in research facilities . . . are provided humane care and treatment.” 7 U.S.C. § 2131(1). The

AWA “authorizes the Secretary of Agriculture to promulgate standards and other requirements governing the humane handling, housing, care, treatment, and transportation of certain animals by

The policy at issue in this case, titled “Annual Inspections for Research Facilities,” and marked “For Internal Use Only,” states: In response to concerns from inspectors about workload, to promote the consistency of our inspections for all research facilities, and to allow us to focus our inspection resources on facilities that present greater risks to animal welfare, in February 2019, we issued guidance that made it mandatory (rather than discretionary) for inspectors to perform focused inspection at AAALAC- accredited research facilities unless the research facility requested a full inspection. This focused inspection counts as the facility’s annual inspection.

(AR03728, “Partial Inspection Policy.”) To avoid confusion, the court will refer to the policy at issue in this case as the Partial Inspection Policy. 3 Throughout this memorandum opinion, citation to document page numbers refer to the page number within the original source, not pagination assigned by the ECF system. dealers, exhibitors, and other regulated entities.” 64 Fed. Reg. 38145 (July 15, 1999). The Secretary of Agriculture delegated responsibility to APHIS to enforce the AWA. Id. 2. AWA Amendment In 1985, Congress recognized that nonhuman primates have psychological and social

needs that are critical to their well-being and acknowledged that the “[c]urrent standards leave too much room for shoddy care and inhumane treatment.” 131 Cong. Rec. 22257 (Aug. 1, 1985) (statement of Sen. Chafee). Further, Congress explained stricter standards were required to protect animals involved in research and experiments. 131 Cong. Rec. 22257 (Aug. 1, 1985). Subsequently, in 1985, Congress passed the Improved Standards for Laboratory Animals Act (“ISLAA”), amending AWA. Pub. L. No. 99-198, 99 Stat. 1645 (1985). ISLAA amended AWA to “ensure that animals necessary for research receive fair and humane treatment, and that their discomfort is kept to an absolute minimum,” while also recognizing that “animal research is essential to the progress of efforts to protect human health.” 131 Cong. Rec. 29274 (Aug. 1, 1985) (statement of Sen. Moynihan). ISLAA requires the Secretary of the USDA to promulgate

standards that “include minimum requirements . . . for a physical environment adequate to promote the psychological well-being of primates.” 7 U.S.C. § 2143(a)(2)(B). ISLAA further provides: “[t]he Secretary shall require each research facility to show upon inspection, and to report at least annually, that the provisions of this Act [7 U.S.C. § 2131, et seq.] are being followed and that professionally acceptable standards governing the care, treatment, and use of animals are being followed by the research facility during actual research or experimentation.” Id. § 2143(a)(7)(A). In complying with the standards set forth in § 2143(a)(7)(A), “research facilities shall provide . . . (i) information on procedures likely to produce pain or distress in any animal and assurances demonstrating that the principal investigator considered alternatives to those procedures; (ii) assurances satisfactory to the Secretary that such facility is adhering to the standards described in this section; and (iii) an explanation for any deviation from the standards promulgated under this section.” Id. § 2143(a)(7)(B). With respect to investigations and inspections involving research facilities, “[t]he Secretary

shall make such investigations or inspections as he deems necessary to determine whether any dealer, exhibitor, intermediate handler, carrier, research facility, or operator of an auction sale subject to section 2142 of this title, has violated or is violating any provision of this chapter or any regulation or standard issued thereunder . . . .” 7 U.S.C. § 2146(a). Further, “[t]he Secretary shall inspect each research facility at least once each year and, in the case of deficiencies or deviations from the standards promulgated under this Act, shall conduct such follow-up inspections as may be necessary until all deficiencies or deviations from such standards are corrected.” Id. Finally, AWA requires that APHIS “make publicly available via searchable database . . . all final [AWA] inspection reports, including all reports documenting all [AWA] violations and non-compliances observed by USDA officials and all animal inventories for the current year and the preceding three

years . . . .” 7 U.S.C. § 2146a(b). 3.

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