Cosette Pharmaceuticals, Inc. v. United States

CourtUnited States Court of Federal Claims
DecidedNovember 17, 2025
Docket25-279
StatusPublished

This text of Cosette Pharmaceuticals, Inc. v. United States (Cosette Pharmaceuticals, Inc. v. United States) is published on Counsel Stack Legal Research, covering United States Court of Federal Claims primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Cosette Pharmaceuticals, Inc. v. United States, (uscfc 2025).

Opinion

In the United States Court of Federal Claims

COSETTE PHARMACEUTICALS, INC., No. 25-cv-279 Plaintiff, Filed Under Seal: October 31, 2025 v. Publication: November 17, THE UNITED STATES, 20251 Defendant.

Travis L. Mullaney of ArentFox Schiff LLP, Washington, D.C. argued for Plaintiff. With him on the briefs were Kevin Pinkney, Richard J. Webber, and Aida Al-Akhdar of ArentFox Schiff LLP, Washington, D.C.

Mikki Cottet of the United States Department of Justice, Civil Division, Washington, D.C. argued for Defendant. With her on the briefs were Yaakov M. Roth, Patricia M. McCarthy and William J. Grimaldi of the United States Department of Justice, Civil Division, Washington, D.C., and Jennifer Claypool and Jason Fragoso of the United States Department of Veterans Affairs.

MEMORANDUM AND ORDER

This action is a bid protest concerning the Department of Veterans Affairs’ (VA’s or

Government’s) efforts to procure prasugrel, a blood thinner used to reduce the risk of heart attacks

and strokes. In this case, the VA seeks to obtain a lower-cost, generic version of the drug because

the brand-name version of prasugrel—manufactured by Plaintiff Cosette Pharmaceuticals, Inc.

(Cosette or Plaintiff)—is significantly more expensive. In procuring the drug, however, the VA

must comply with federal law which mandates, with discrete exceptions, that the drug be

1 This Memorandum and Order was filed under seal on October 31, 2025, in accordance with the Protective Order entered in this case. ECF No. 43. On November 14, 2025, the parties filed a Notice proposing redactions to the Memorandum and Order. ECF No. 45. The sealed and public versions of this Memorandum and Order are identical, except for some redactions, this footnote, and the addition of the publication date.

1 manufactured in the United States or certain approved countries. In particular, the Trade

Agreements Act of 1979, 19 U.S.C. §§ 2501 et seq., (TAA) constrains the agency’s choices. The

statute prohibits federal agencies from purchasing products manufactured in certain countries,

unless, as relevant to this action (i) no statutorily-compliant alternative is offered, or (ii) the

compliant alternatives are “insufficient” to fulfill the Government’s requirements. 19 U.S.C.

§ 2512(a)(2). Despite receiving a TAA-compliant offer from Cosette, which manufactures its

prasugrel in Germany,2 a compliant country under the TAA, the VA nevertheless awarded the

contract to Golden State Medical Supplies, Inc. (Golden State), which manufactures its generic

version of prasugrel in India, a non-compliant country under the TAA. Cosette challenges that

award here, contending that since it submitted the only TAA-compliant offer, the VA was bound

by law to (i) award Cosette the contract for the supply of prasugrel, (ii) procure the drug via the

current Federal Supply Schedule contract with Cosette, or (iii) cancel the Solicitation and procure

a generic form of prasugrel on the open market. In contrast, despite the TAA’s prohibition on

purchasing products manufactured in India, the VA contends that the award to Golden State is

nevertheless permissible under one of the TAA’s above-referenced statutory exceptions because

Cosette’s significantly higher price rendered its offer “insufficient to fulfill the requirements of the

United States Government.” See ECF No. 29 at 29 (Def. MJAR); 19 U.S.C. § 2512(a)(2)(B).

2 Cosette performs its final manufacturing in Germany, while its active pharmaceutical ingredient (API) comes from Japan. ECF No. 27 at 12 (Plaintiff’s Motion for Judgment on the Administrative Record). Under the TAA’s definition, a product comes from the last country where “it has been substantially transformed.” 19 U.S.C. § 2518(4)(B). Cosette acknowledges that the manufacture of the API (rather than the final manufacture) has historically been the country of the last substantial transformation but argues that the place of final manufacture “may also be relevant.” ECF No. 27 at 12 n.1. As both Germany and Japan are TAA-compliant countries, the parties do not dispute that Cosette’s prasugrel is TAA-compliant. See ECF No. 29 at 15 (Defendant’s Cross- Motion for Judgment on the Administrative Record).

2 Resolution of this dispute turns on whether an offer is “insufficient” under the TAA if it

would impose significantly greater expenses on the agency (i.e., Cosette’s offer) than would an

otherwise non-TAA-compliant alternative (i.e., Golden State’s offer). In urging the Court to rule

in its favor, the VA advances many policy rationales, many of them seemingly well-founded;

however, it is evident that Congress opted not to write such a “high price” exception into the plain

text of the TAA. However much the VA may prefer a lower price—and however laudable the

VA’s policy reasons to protect the public fisc may be—the agency is bound to the framework

Congress enacted. The VA must comply with the TAA when making its award decision, and this

Court is similarly bound to interpret laws as enacted by Congress, regardless of any compelling

policy rationales the VA advances to the contrary.

Accordingly, for the reasons described below, Cosette’s Motion for Judgment on the

Administrative Record (ECF No. 27) is GRANTED IN PART and the VA’s Cross-Motion for

Judgment on the Administrative Record (ECF No. 29) is DENIED IN PART.

BACKGROUND

I. Statutory and Regulatory Context

Two relevant statutes limit the Government’s ability to purchase goods originating abroad.

Acetris Health, LLC v. United States, 949 F.3d 719, 722-23 (Fed. Cir. 2020). The first, the Buy

American Act of 1933 (BAA), 41 U.S.C. §§ 8301-8305, was enacted during the Great Depression

“to create jobs for American workers and protect American industry.” United States v. Rule Indus.,

Inc., 878 F.2d 535, 538 (1st Cir. 1989). The BAA requires federal agencies to acquire “only

manufactured articles, materials, and supplies that have been manufactured in the United States,”

unless the head of the procuring agency determines that doing so would be inconsistent with the

3 public interest, would result in unreasonable cost,3 or that suitable domestic products are not

available in sufficient quantity or quality. 41 U.S.C. § 8302(a)(1).

As noted, this bid protest turns in large part on the construction and application of the

second statute, the Trade Agreements Act of 1979, 19 U.S.C. §§ 2501 et seq., and its implementing

regulations. The Trade Agreements Act of 1979 was enacted in part to implement the United

States’ commitments under international trade agreements, including the World Trade

Organization Government Procurement Agreement (WTO GPA)—a multilateral trade agreement

that requires signatory countries to open government procurement markets to one another on equal

and nondiscriminatory terms. 19 U.S.C.

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