Cardiovascular Diagnostics, Inc. v. Boehringer Mannheim Corp.

985 F. Supp. 615, 1997 U.S. Dist. LEXIS 18096, 1997 WL 709979
CourtDistrict Court, E.D. North Carolina
DecidedNovember 10, 1997
Docket5:97-cv-00174
StatusPublished
Cited by3 cases

This text of 985 F. Supp. 615 (Cardiovascular Diagnostics, Inc. v. Boehringer Mannheim Corp.) is published on Counsel Stack Legal Research, covering District Court, E.D. North Carolina primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Cardiovascular Diagnostics, Inc. v. Boehringer Mannheim Corp., 985 F. Supp. 615, 1997 U.S. Dist. LEXIS 18096, 1997 WL 709979 (E.D.N.C. 1997).

Opinion

ORDER

BRITT, District Judge.

This matter is before the court on the following motions: (1) defendant’s motion for judgment on the pleadings on counts II through VI of the complaint; (2) plaintiffs motion for judgment on the pleadings on count I of the complaint and defendant’s counterclaim; (3) defendant’s motion to file an amended counterclaim; and (4) defendant’s motion for partial summary judgment on the issue of implied license.

I. Background

Plaintiff Cardiovascular Diagnostics Inc. (“CDI”) is a North Carolina-based company involved in developing medical technology to aid in diagnosing human cardiovascular problems. Boehringer Mannheim Corporation (“BMC”) is an Indiana company also engaged in the medical diagnostics business. The technology at issue in this dispute involves processes to measure blood coagulation. At some point after its founding in 1986, CDI created a system of assays to evaluate blood coagulation time. Specifically, CDI developed tests to evaluate prothrombin time (PT) and activated partial thromboplastin time (aPTT). Seeking access to the methodology and equipment developed by CDI, BMC pursued a license agreement with the company.

Effective 21 June 1989, the two companies consummated a License Agreement (“Agreement”) authorizing BMC to serve as the exclusive licensee of CDI technology involving *617 PT and aPTT assay systems. (Agreement, ¶2.1.) The Agreement also gives BMC a ninety-day exclusive right to evaluate new CDI technology and thirty additional days to engage in negotiations to license such technology. (Id. ¶ 6.2.) If BMC declined to license new technology involving a thrombolytic assay and CDI paid a $1,000 fee to BMC, CDI could then use its technology in the field of PT and aPTT assay systems “in connection with and as a part of such thrombolytic assays.” (Id. ¶ 6.2.1.) Section VII of the Agreement contains a confidentiality provision mandating secrecy with regard to certain information and materials exchanged during the relationship. (Id. § VII.) The terms of the Agreement are to “remain in full force and effect for 10 years.” (Id. ¶ 8.1.)

Several years later, disputes arose regarding the operation of the Agreement. In particular, the parties disagreed about CDI’s right to use the licensed technology. After considerable negotiation, in September 1995, the parties executed a “First Amendment to License Agreement” (“Amendment”). The Amendment provides that, pursuant to the original Agreement, BMC did not license thrombolytic assays submitted to it by CDI and received a $1,000 payment from CDI. (Amendment, ¶ 6.2.2.) BMC and CDI then agreed that CDI could use this technology with

no limitation on the manufacture, use, sale or rights of others to manufacture, use or sell PT and aPTT tests and systems as long as such tests and systems are sold to customers using analyzers which are capable of analyzing, among other things, each of (i) a PT or aPTT test, and (ii) a thrombolytic test.

(Id. ¶2.) The Amendment also contains the following language:

Each of BMC and CDI do hereby release the other party, its officers, agents, employees, successors and assigns from any claims, demands, actions, suits, damages, liabilities, losses or expenses of whatever sort, relating to or in connection with the License Agreement for acts or omissions by either BMC or CDI prior to the date of this First Amendment to the License Agreement.

(Id. ¶ 5.)

Prior to the Amendment, BMC had acquired the rights in two patents (“'779 patent and '598 patent”) apparently dealing with coagulation assays from Biotrack, Inc. in 1994. BMC has informed CDI that it believes that CDI’s products infringe both the '779 patent and the '598 patent. CDI now brings suit seeking, in count I, a declaration of noninfringement, invalidity, or unenforceability concerning two patents owned by BMC. CDI also alleges that BMC breached the confidentiality agreement when it disclosed CDI’s trade secrets in two United States patents and six international patent applications published in March 1995. Throughout this process, CDI maintains that BMC actively and intentionally misappropriated CDI’s technology in direct violation of their Agreement. This conduct serves as the basis for counts II-VI alleging breach of contract, breach of fiduciary duty, constructive fraud, trade secrets, and unfair and deceptive trade practices. BMC counterclaimed that a device manufactured and sold by CDI, the Thrombolytic Assay System, infringes BMC’s '598 and '779 patents.

The court now turns to the motions at hand.

II. Standard

Rule 12(c) of the Federal Rules of Civil Procedure provides that a motion for judgment on the pleadings shall be treated as one for summary judgment if matters outside of the pleadings are offered and considered by the court. Fed.R.Civ.P. 12(c). In this instance, because of the relevant defenses to a release provision, the court finds it both necessary and proper to consider matters outside of the pleadings with respect to BMC’s motion for judgment on the pleadings. At the same time, supporting documents have accompanied the respective briefs regarding CDI’s motions for judgment on the pleadings and it also should be converted. Therefore, pursuant to Federal Rule of Civil Procedure 56(e), summary judgment is appropriate where there are no genuine issues as to any material facts and the moving party is entitled to judgment as a matter of law. Fed. *618 R.Civ.P. 56(c). The Fourth Circuit has articulated the summary judgment standard as follows:

A genuine issue exists “if the evidence is such that a reasonable jury could return a verdict for the nonmoving party.” Anderson v. Liberty Lobby, Inc., 477 U.S. 242, 248, 106 S.Ct. 2505, 2510, 91 L.Ed.2d 202 (1986). In considering a motion for summary judgment, the court is required to view the facts and draw reasonable inferences in a light most favorable to the nonmoving party. Id. at 255, 106 S.Ct. at 2514. The plaintiff is entitled to have the credibility of all his evidence presumed. Miller v. Leathers, 913 F.2d 1085, 1087 (4th Cir.1990), cert. denied, 498 U.S. 1109, 111 S.Ct. 1018, 112 L.Ed.2d 1100 (1991). The party seeking summary judgment has the initial burden to show absence of evidence to support the nonmoving party’s case. Celotex Corp. v. Catrett, 477 U.S. 317, 325, 106 S.Ct. 2548, 2554, 91 L.Ed.2d 265 (1986).

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985 F. Supp. 615, 1997 U.S. Dist. LEXIS 18096, 1997 WL 709979, Counsel Stack Legal Research, https://law.counselstack.com/opinion/cardiovascular-diagnostics-inc-v-boehringer-mannheim-corp-nced-1997.