MSP CORP. v. Westech Instruments, Inc.

500 F. Supp. 2d 1198, 2007 U.S. Dist. LEXIS 57988, 2007 WL 2253473
CourtDistrict Court, D. Minnesota
DecidedAugust 6, 2007
DocketCivil 07-2301 (MJD/SRN)
StatusPublished
Cited by6 cases

This text of 500 F. Supp. 2d 1198 (MSP CORP. v. Westech Instruments, Inc.) is published on Counsel Stack Legal Research, covering District Court, D. Minnesota primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
MSP CORP. v. Westech Instruments, Inc., 500 F. Supp. 2d 1198, 2007 U.S. Dist. LEXIS 57988, 2007 WL 2253473 (mnd 2007).

Opinion

PRELIMINARY INJUNCTION

DAVIS, District Judge.

I. INTRODUCTION

This matter is before the Court on Plaintiff MSP Corporation’s Motion for Preliminary Injunction. [Docket No. 6] The Court heard oral argument on July 27, 2007.

II. BACKGROUND

A. Factual Background

1. Parties

Plaintiff MSP Corporation (“MSP”) is a Minnesota corporation located in Shore- *1204 view, Minnesota, with 40 employees. It sells products internationally that are used in the semiconductor, pollution control, and pharmaceutical industries.

Defendants Westech Instruments, Inc., a Georgia corporation; Westech Instrument Services Ltd., a United Kingdom corporation; and Westech Instrument Holdings, PLC, a United Kingdom corporation, (collectively “Westech”) market and manufacture aerosol testing devices, including impactors. Defendant Westech Instruments, Inc., is the United States distributor for Westech products.

Westech promotes its products in the United States and Minnesota through the internet and also markets directly to Minnesota residents through direct email advertisements.

2.Impactor Product and Development of the Next Generation Im-pactor

Certain inhaled medications are dispensed through aerosol or powder inhalers. In order to create metered-dose and dry-powder inhalers, pharmaceutical companies must measure the quantity and particle size of the medication dispensed in each dose. An impactor is a device that measures the size of aerosol particles and is used by pharmaceutical companies to test inhalers.

Until the end of the 1990s, pharmaceutical companies used impactor technology that was developed for military applications in the 1940s. This impactor was called the Andersen Impactor or the Andersen Cascade Impactor (“ACI”) and was not precise. The Andersen Impactor functioned by forcing the aerosol or powder through a seiies of stages or “cascades” designed to sort particles.

Due to the accuracy problems of the Aidersen Impactor, a consortium of 15 pharmaceutical companies, called the Next Generation Impactor Consortium (“the Consortium”) was founded to fund research and development of a new impactor. The Consortium selected MSP to develop the new impactor. In 1998, MSP entered into a written contract with Consortium representative Glaxo-Wellcome Research and Development Limited (“Glaxo”) to develop the new impactor (“Glaxo Contract”).

3. Glaxo Contract

Under the Glaxo Contract, the Consortium paid MSP $950,000. The Glaxo Contract also required that the new impactor design, called the Next Generation Impactor or “NGI,” be published in peer-reviewed journals and/or the Pharmacopoeia, including the specific design requirements and full dimension drawings. The Glaxo Contract also required MSP to use “its best commercial efforts to reduce the manufacturing cost and final price” of the NGI.

The Glaxo Contract requires MSP, after having sold its first 100 units, “to make available all INTELLECTUAL PROPERTY resulting from [the Glaxo Contract] ... necessary for the manufacture of NGIs or further embodiments of the NGI for use or sale only in the pharmaceutical industry ... [and] to license upon reasonable terms and conditions [to] third parties reasonably able to manufacture NGIs to provide additional source(s) of NGIs for the [pharmaceutical] industry.” MSP’s licensing obligation extends to all patents, copyrights, and designs that may cover NGIs and survives termination of the NGI Contract.

4. The Next Generation Impactor

In 2000, MSP introduced a prototype new impactor called the Next Generation Impactor (“NGI”). The NGI improved the reliability, accuracy, and efficiency of particle measurement. While the Andersen Impactor had a vertical cylindrical design, MSP set the cascade stages in a flat hori *1205 zontal design. MSP created a puzzle-piece shape for the NGI that traces the shape of the internal components of the NGI, but MSP avers that design could have been a rectangle or square, and the puzzle shape had no impact on the device’s performance. It also made the bottom of the outside of the NGI royal blue, to match MSP’s company colors and logo.

After extensive testing, the Consortium approved MSP’s second prototype, the NGI, as a standard-setting measurement device, and the FDA accepts measurements taken by the NGI device as accurate and reliable. Almost all new impactors purchased by pharmaceutical companies are MSP’s NGI device, and MSP has sold more than 400 NGI devices.

There are a number of other types of impactors on the market, as well, such as the ACI, the Marple-Miller Impactor, and the Multi-Stage Liquid Impinger. Several manufacturers make and sell their own versions of these different impactors. For example, Westech and Copley Scientific (“Copley”) both make and sell the Andersen Cascade Impactor. Those in the pharmaceutical industry are aware that multiple companies make and sell the same type of impactor.

According to Westech, the weight of the impactor is an important feature and some customers are willing to pay more for a lighter titanium device, such as the versions of Andersen Cascade Impactors sold by Westech and Copley. Also according to Westech, impactor consumers are usually well-educated persons working at sophisticated pharmaceutical companies.

5. MSP’s Treatment of Its Intellectual Property

MSP had authority under the Glaxo Contract to seek protection for any intellectual property; however, MSP did not seek trademark or trade dress protection for any of the marks relevant in this lawsuit. Additionally, MSP does not use the common law trademark designation (TM) with any of the marks at issue in this case, although it uses the TM designation with other products that it offers.

6. Westech’s Competing Product

a. Westech’s Product

Westech asserts that it created its own NGI with the support of Pfizer Global R & D Ltd. (“Pfizer”), an original Consortium member. Westech modeled its device from the NGI specifications approved by the NGI Consortium and disclosed in the European Pharmacopoeia (“EP”). The United States Pharmacopoeia (“USP”) and EP are the official texts containing the standards for all prescription and over-the-counter medicines, dietary supplements, and other healthcare products and devices manufactured and sold in Europe and the United States. The specifications included the dimensions of the preseparator, the nozzle diameters of the jet stages, the micro-orifice collector, the cup depth, the collection cup surface roughness, and the nozzle to seal body distances. Westech also matched the shape of the housing to the shape of the jet stages and the inter-stage flow channels, in part, it claims, to reduce the weight of the device.

b. Westech’s Interaction with MSP

On January 9, 2007, Westech requested a meeting with MSP to discuss issues before Westech made a formal request to MSP to license the manufacture of the NGI.

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500 F. Supp. 2d 1198, 2007 U.S. Dist. LEXIS 57988, 2007 WL 2253473, Counsel Stack Legal Research, https://law.counselstack.com/opinion/msp-corp-v-westech-instruments-inc-mnd-2007.