Facta Health Inc v. Pharmadent LLC

Court of Appeals for the Third Circuit·Decided September 30, 2024·No. 23-2224·Unpublished

Opinion

NOT PRECEDENTIAL

UNITED STATES COURT OF APPEALS FOR THE THIRD CIRCUIT

No. 23-2224

FACTA HEALTH INC; FRANK J. COZZARELLI; ROBERT MANGONE;

PAUL KAPP; ROBERT LAUDADIO; GOTTA GUY INC, Appellants

v.

PHARMADENT LLC; ALAN WICKENHAUSER;

STEPHEN PEIPERT

On Appeal from the United States District Court for the District of New Jersey (D.C. Civil No. 2-20-cv-09631)

District Judge: Honorable Stanley R. Chesler

Submitted Pursuant to Third Circuit L.A.R. 34.1(a)

on April 12, 2024

Before: CHAGARES, Chief Judge, PORTER, and SCIRICA, Circuit Judges.

(Filed: September 30, 2024)

OPINION *

*

This disposition is not an opinion of the full Court and pursuant to I.O.P. 5.7 does not constitute binding precedent.

SCIRICA, Circuit Judge After a four-day hearing, an American Arbitration Association Panel found that Facta Health, Inc. breached its Patent Purchase Agreement with Pharmadent, LLC. The Panel rescinded the agreement and returned the intellectual property to Pharmadent, but also permitted Pharmadent to keep Facta’s initial payment. Pharmadent and its members Dr. Alan Wickenhauser and Stephen Peipert moved to confirm the Final Award, and Facta and its principals Frank J. Cozzarelli, Robert Mangone, Paul Kapp, Robert Laudadio, and Gotta Guy, Inc. moved to vacate it. The District Court confirmed the Final Award. Facta now appeals the District Court’s judgment. Because the District Court did not err in confirming the Final Award, we will affirm.

I.

Facta and Pharmadent entered into a Patent Purchase Agreement (“PPA”), under which Pharmadent sold Facta patents and intellectual property for a topical anesthetic developed by Wickenhauser and Peipert. In exchange, Pharmadent would receive a $400,000 initial payment and a royalty payment plan, which included a $3,000,000 advance upon the product’s approval by the Food and Drug Administration (“FDA”) or the Department of Defense (“DOD”). The PPA provided that the Parties would resolve any dispute before a three-member American Arbitration Association (“AAA”) Panel under its Commercial Arbitration Rules. The PPA further provided that the hearing conducted by the Panel would last no longer than a day, but that the time limit was not jurisdictional and could be extended for good cause. Finally, the PPA specified that Pharmadent’s remedies included, inter alia, rescission of the agreement if Facta failed to

pay the royalty fee, as well as “equitable relief, which may be appropriate in the circumstances.” App. 1369.

Although the PPA contemplated the Parties’ cooperation in seeking the product’s approval, the relationship soured, leading to an arbitration, state court proceeding, and two amendments to the PPA. The relationship deteriorated further, and Facta initiated a second arbitration and state court action. Pharmadent removed the matter to federal court on diversity grounds, where the District Court granted its motion to stay the litigation and compel arbitration. In the arbitration, Pharmadent asserted counterclaims, including breach of contract and breach of the implied covenant of good faith and fair dealing, and sought, inter alia, rescission of the PPA and return of the intellectual property.

The Panel determined that due to the number of witnesses the Parties wished to present, good cause existed to schedule ten days of evidentiary hearings, which the Panel later reduced to four days. Facta also filed thirteen applications for pre-hearing dispositive motions, which the Panel denied.

In its pre-hearing briefing, Facta urged the Panel to apply certain legal doctrines when it interpreted the PPA and addressed issues in the dispute. Facta also asserted that Dr. Robert Lake, the regulatory director of Pharmadent, should be prohibited from offering an expert report and testimony. During the four-day hearing, the Panel heard testimony from four witnesses and considered some 350 exhibits. The Panel addressed Facta’s contentions respecting Lake’s testimony, explaining that it would assign the report and testimony “the weight [it] believe[d] is appropriate.” App. 980. At the conclusion of the hearing, Facta’s counsel confirmed that Facta was satisfied that it had

the opportunity to present its case to the Panel.

Upon consideration of the Parties’ arguments presented at the hearing, as well as their pre- and post-hearing briefing, the Panel issued a Final Award in favor of Pharmadent and rejected all Facta’s claims. Notably, the Panel rejected Facta’s fraudulent inducement claim and other “vague allusions to [Pharmadent’s] . . . fraud,” App. 330, explaining that Facta’s principals testified that Pharmadent “had not made any intentional misrepresentation to, or concealed any information from, Facta,” App. 331. The Panel concluded that Facta breached the PPA by terminating Wickenhauser from his role in overseeing the approval process and that Facta breached the implied covenant of good faith and fair dealing by “repeatedly and intentionally interfer[ing] with Pharmadent’s ability to lead and control the DOD/FDA approval and testing process[].” App. 324, 327. Observing that the Parties agreed that the PPA entitled Pharmadent to equitable relief, and that the plain language of the PPA vested the Panel with “the sound discretion” to fashion “the specific parameters of any equitable remedy,” the Panel rescinded the PPA and assigned the intellectual property to Pharmadent. App. 335. The Panel also permitted Pharmadent to keep the initial payment, concluding that Pharmadent’s retention of the payment “equitably addresse[d]” Facta’s “wrongful conduct in frustrating and delaying Pharmadent’s pursuit of FDA approval,” which “deprived Pharmadent . . . of the opportunity to enjoy the potential rewards of DOD/FDA approval and reduced the remaining life of” the patents. App. 337.

The District Court granted Pharmadent’s motion to confirm the Final Award and denied Facta’s cross-motion to vacate, finding that Facta’s arguments did not warrant

vacatur under 9 U.S.C. § 10(a). Facta Health, Inc. v. Pharmadent, LLC, No. CV 20-9631 (SRC), 2023 WL 3965921, at *3 (D.N.J. June 13, 2023).

Facta timely appealed.

II.

As a threshold matter, Facta argues that the District Court may have lacked subject matter jurisdiction. Facta explains that when Pharmadent removed on the stated basis of diversity jurisdiction, Wickenhauser filed a declaration that he and Peipert were the only two members of Pharmadent. Facta argues that this declaration is suspect because some four months later, Wickenhauser submitted a new drug application to FDA in which he wrote that Pharmadent consisted of four members.

Diversity jurisdiction must exist at the time the complaint was filed and at the time of removal, and the burden is on the moving party to establish federal jurisdiction. Johnson v. SmithKline Beecham Corp., 724 F.3d 337, 346 (3d Cir. 2013). Wickenhauser’s declaration established complete diversity among the Parties, and there was no contrary evidence in the record at the time of removal. See Lincoln Ben. Life Co. v. AEI Life, LLC, 800 F.3d 99, 105 (3d Cir. 2015) (explaining that for diversity purposes, a limited liability company is a citizen of every state in which a member is a citizen). Facta does not explain how the new drug application demonstrates that Pharmadent failed to meet its burden to establish jurisdiction at the time of removal.

Accordingly, the District Court exercised diversity jurisdiction over the matter under 28 U.S.C. §§ 1332(a) and 1441(b). We have jurisdiction under 28 U.S.C. § 1291 and the Federal Arbitration Act. See 9 U.S.C. § 16(a)(1)(D) (“An appeal may be taken

from . . . an order . . . confirming or denying confirmation of an award or partial award . . . .”).

III.

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