HESKA CORPORATION v. QORVO US, INC.

CourtDistrict Court, M.D. North Carolina
DecidedSeptember 30, 2020
Docket1:19-cv-01108
StatusUnknown

This text of HESKA CORPORATION v. QORVO US, INC. (HESKA CORPORATION v. QORVO US, INC.) is published on Counsel Stack Legal Research, covering District Court, M.D. North Carolina primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
HESKA CORPORATION v. QORVO US, INC., (M.D.N.C. 2020).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE MIDDLE DISTRICT OF NORTH CAROLINA

HESKA CORPORATION, ) ) Plaintiff, ) ) v. ) 1:19CV1108 ) QORVO US, INC., ) ) QORVO BIOTECHNOLOGIES, LLC, ) ) and, ) ) ZOMEDICA PHARMACEUTICALS INC., ) doing business as ) ZOMEDICA PHARMACEUTICALS CORP., ) ) Defendants. )

MEMORANDUM OPINION AND ORDER

LORETTA C. BIGGS, District Judge. Plaintiff, Heska Corporation (“Heska”), initiated this action on November 1, 2019, against Defendants, Qorvo US, Inc. (“Qorvo US”), Qorvo Biotechnologies, LLC (“Qorvo Biotech”),1 and Zomedica Pharmaceuticals Inc. (“Zomedica”), alleging misappropriation of trade secrets under both federal and state statutes. (ECF No. 1.) Before the Court are Defendants’ Motion to Dismiss pursuant to Rule 12(b)(6) of the Federal Rules of Civil Procedure, (ECF No. 11), and Plaintiff’s Motion to Disregard or Strike, (ECF No. 18). For the reasons stated below, Defendants’ motion will be denied, and Plaintiff’s motion will be granted.

1 Throughout this Memorandum Opinion and Order, Qorvo US and Qorvo Biotech are collectively referenced as “Qorvo.” I. BACKGROUND On November 22, 2019, Plaintiff filed an Amended Complaint that now serves as the operative complaint in this action and from which much of the background is derived. (ECF

No. 8.) Plaintiff is a Delaware corporation with its principal place of business in Colorado and is in the business of selling supplies and equipment used in the veterinary medicine industry. (Id. ¶¶ 1, 9.) In 2011, Plaintiff entered into a business relationship with Rapid Diagnostek, Incorporated (“RDI”)2 in an effort to develop an instrument (“Instrument Product”) that would allow veterinary professionals to perform diagnostic testing “at point of treatment, rather than requiring the animal patients to be transported into a veterinary clinic.”

(Id. ¶¶ 11, 14–15.) Heska and RDI executed two ten-year contracts memorializing their business relationship—the Research, Development, and Distribution Agreement (“RDDA”) and the Manufacturing and Supply Agreement (“MSA”) (collectively “the Agreements”). (Id. ¶¶ 11–12, 22.) Though the Agreements have not been made a part of the record, according to the Amended Complaint the terms provide that Heska was responsible “for funding development

costs associated with RDI’s research and development program in accordance with a Schedule of Milestones set forth in the RDDA” and for “the development and supply of certain reagents necessary for RDI’s development of the Instrument Product.” (Id. ¶¶ 19–20.) Further, the MSA provides Heska with the exclusive right to purchase the Instrument Product from RDI at specified prices and quantities and the exclusive right to market it. (Id. ¶ 21.) The

2 RDI is not a party to this lawsuit. Agreements also contained provisions “prohibiting the use and disclosure” of information associated with the development of the Instrument Product. (Id. ¶¶ 75, 85, 93, 99.) The Amended Complaint alleges that, up until about mid-2016, Plaintiff and RDI carried

out their respective obligations under the Agreements and would regularly meet to discuss the development of the Instrument Product. (Id. ¶¶ 34–36.) On October 17, 2016, Plaintiff received an e-mail notifying it that RDI was in liquidation. (Id. ¶ 38.) A few weeks later, on November 3, 2016, Plaintiff was notified by e-mail that Qorvo had purchased physical assets and IP from RDI, hired RDI’s technical team, and that “RDI contracts were not included in the sale.” (Id. ¶ 40.)

Heska subsequently filed suit in Colorado state court against RDI for breach of contract and injunctive relief related to the Agreements. (Id. ¶ 55.) Plaintiff was granted an injunction against RDI and subsequently sought third party discovery from Qorvo US to learn more information about the RDI-Qorvo Asset Purchase Agreement (“APA”). (Id. ¶¶ 43, 55–57.) Plaintiff sought to determine whether Qorvo US took partially completed Heska/RDI research and continued to work toward completion of the project though it initially was met

with resistance. (Id. ¶¶ 43–44.) At some point, Qorvo US permitted Heska’s technical employees to review portions of the APA who ascertained that Qorvo US acquired “many items of tangible personal property and inventories” including “items that Heska and RDI were working on together pursuant to the RDDA and MSA.” (Id. ¶ 49.) As a result of that review, Heska alleges that Qorvo US obtained through their acquisition of RDI a prototype, components of an incomplete prototype, and items related to the prototypes. (Id. ¶ 50.)

Further, Plaintiff alleges “that upon information and belief, Qorvo US transferred or assigned the tangible assets and intellectual property it obtained from RDI to Qorvo Biotech, who in turn transferred or assigned it to Zomedica.” (Id. ¶ 52.) Plaintiff also alleges that Qorvo Biotech’s parent company, Qorvo, Inc., hired RDI’s principal research and development

scientist who had directly worked with Heska on the Instrument Product’s development for the five years that Heska and RDI collaborated. (Id. ¶ 51.) On or about November 27, 2018, Zomedica announced it entered into an agreement with Qorvo Biotech to develop a veterinary diagnostic tool—later named “Truforma®”—“with the goal to deliver reference-lab performance at the point of care.”3 (Id. ¶ 59.) The Amended Complaint alleges that the November 2018 press release indicates that Truforma® relies on a

sensor which “is the same kind of resonator developed for the Instrument Product,” neither of which relies on the industry-standard optical or fluorescence-based approach. (Id. ¶ 64.) Finally, the Amended Complaint alleges that Truforma(R)’s “dimensions and shape are virtually identical to the most recent prototype Heska developed with RDI under the RDDA.” (Id. ¶ 65.) Plaintiff filed this action, alleging misappropriation of trade secrets, following the

development of the Truforma® instrument, which Plaintiff argues builds upon Heska’s trade secrets obtained by Qorvo US when it acquired RDI. II. PLAINTIFF’S MOTION TO STRIKE As a preliminary matter, before addressing the merits of Defendants’ Motion to Dismiss, the Court will address Plaintiff’s Motion to Strike. Plaintiff moves this Court to

3 While the November 27, 2018, press release refers to the device being able to deliver “point-of-care” diagnostic information, (ECF No. 8-2 at 1), the Court understands this to be the same as “point of treatment”— meaning that rather than requiring an animal to come to an office or clinic setting, veterinary medicine professionals would be able to perform diagnostic testing and analysis where the animal is located or housed. strike, or otherwise disregard, Section II of Defendants’ Reply Brief pursuant to NCMD Local Rule 7.3(h). (ECF No. 18.) In support of its motion, Plaintiff argues that Defendants’ Reply Brief raises new

arguments not contained in its prior briefing in violation of Local Rule 7.3(h). (ECF No. 19 at 1–2.) Specifically, Plaintiff argues that Defendants’ original brief did not argue, nor did Plaintiff’s Response assert or implicate, Heska’s ownership of, or claim conversion theory relating to, the alleged trade secrets that are the subject of Plaintiff’s Amended Complaint. (Id. at 5.) In addition, according to Plaintiff, Defendants introduced two new statutes for the first time to support these new arguments. (Id. at 4.) Defendants contend in response that the

arguments in their Reply Brief are consistent with arguments contained in their initial brief in support of their Motion to Dismiss.

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