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`IN THE UNITED STATES DISTRICT COURT
`FOR THE WESTERN DISTRICT OF WISCONSIN
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`The DeLong Co., Inc.
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`Plaintiff,
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`vs.
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`Syngenta AG,
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`Syngenta Crop Protection AG,
`Syngenta Corporation,
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`Syngenta Crop Protection, LLC,
`Syngenta Biotechnology, Inc., and
`Syngenta Seeds, LLC,
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`Defendants.
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`JURY TRIAL DEMANDED
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`THE DELONG CO., INC.’S ORIGINAL COMPLAINT
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`The DeLong Co., Inc. (“DeLong” or “Plaintiff”) for its Complaint against Syngenta AG
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`Case No. 17-cv-778
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`(“Syngenta AG”), Syngenta Crop Protection AG (“Crop Protection AG”), Syngenta Corporation
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`(“Syngenta Corp.”), Syngenta Crop Protection, LLC (“Crop Protection LLC”), Syngenta Seeds, Inc.
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`(“Syngenta Seeds”) (now known as Syngenta Seeds, LLC), and Syngenta Biotechnology, Inc.
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`(“Syngenta Biotech”) (now merged with Crop Protection, LLC, with Crop Protection, LLC, as the
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`survivor) (Syngenta AG, Crop Protection AG, Syngenta Corp. Crop Protection LLC, Syngenta Seeds
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`and Syngenta Biotech are sometimes hereinafter collectively referred
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`to as “Syngenta” or
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`“Defendants”), allege, on personal knowledge as to themselves and on information and belief as to all
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`other matters, as follows:
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`NATURE OF THE ACTION
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`Biotechnology holds promise to potentially improve the lives of many. But it also can cause
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`extraordinary harm if handled irresponsibly.
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`Part of acting responsibly requires that biotechnology companies avoid introducing a new
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`genetic trait into the market prematurely before it has been approved in all significant export markets.
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`All in the industry, including Syngenta, recognize that premature commercialization can cause
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`significant trade disruptions and enormous harm to farmers and other industry participants. That is why
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`they have pledged to each other and to other stakeholders, including both corn farmers and other
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`industry participants, that they will act responsibly in introducing new bio-engineered genetic traits into
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`the market.
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`Syngenta had the opportunity to act responsibly in 2010. Its new genetically modified corn
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`Agrisure Viptera®, containing the MIR162 genetic trait, had just been deregulated by the United States
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`Department of Agriculture (“USDA”). But Syngenta was aware that a large and growing export market
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`for U.S. corn and corn products, China, had not approved MIR162. In fact, Syngenta had only that same
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`year sought regulatory approval in China, and at the time, the average time for regulatory approval in
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`China was 2-3 years. The process is longer if applications are incomplete or incorrect. And Syngenta’s
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`were. Syngenta had been previously warned by industry participants not to introduce another MIR
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`genetic trait because of lack of approval in export markets, and the devastating consequences that could
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`occur from such premature commercialization.
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`But Syngenta also knew that the clock was ticking on expiration of its patent for this genetic
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`trait. Every year that passed without commercialization meant lost monopoly profits granted by patent.
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`Syngenta had a decision to make. It could wait until China approved its new genetic trait and
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`temporarily forego its monopoly profits. That is what it had pledged to do, and what responsible
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`practice in any event dictated. Or Syngenta could immediately commercialize Agrisure Viptera®, and
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`create an enormous risk that U.S. corn farmers (also known as “Producers” as defined in the Court’s
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`March 10, 2015 Order (ECF No. 287 at 4) and other industry participants (also known as “Non-
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`Producers”) would lose one of their large and growing export markets.
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`Sadly, Syngenta opted for its monopoly profits over responsibility to its stakeholders. It chose to
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`commercialize Viptera® for the 2011 crop year knowing that China would not approve MIR162 until
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`sometime after that trait had entered export channels.
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`During 2011 – 2013, Syngenta was called upon again by industry participants to show
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`responsibility and stop its overly aggressive commercialization. China’s importance as a purchaser of
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`U.S. corn and corn products had continued to grow and it still had not approved MIR162. Syngenta’s
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`response was to expand sales for the 2012 and 2013 growing seasons, and capture more monopoly
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`profits.
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`In November 2013, the very occurrence that had been foreseen by industry participants,
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`including Syngenta, occurred. U.S. exports to China were found to be contaminated with MIR162,
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`which still had not been approved by China. China therefore began rejecting shipments of corn from the
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`U.S. Shipment of distillers dried grain with solubles (DDGS), a byproduct of corn ethanol production
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`sold by many industry participants, were similarly rejected and became subject to a prohibitive
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`certification process in the summer of 2014.
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`After rejection of U.S. corn and corn product shipments, industry participants in early 2014
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`demanded that Syngenta immediately halt commercialization of Agrisure Viptera®. They also
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`demanded that Syngenta not commercialize a brand new product, Agrisure Duracade™, which also
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`contained MIR162 and a new event, not approved by China and other export markets -- Event 5307.
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`The industry participants pointed out that they were “gravely concerned about the serious economic
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`harm” to those in the industry, including both corn Producers and Non-Producers, caused by the loss of
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`the Chinese market. At that time, the National Grain and Feed Association quantified the economic
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`harm as already ranging from $1 billion to $2.9 billion.
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`Syngenta doubled down. It continued to sell Agrisure Viptera®, and launched Agrisure
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`Duracade™ for the 2014 crop year, thereby prolonging the economic harm indefinitely. Those
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`irresponsible actions also ensured that the economic losses to farmers and others in the industry would
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`continue to grow.
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`These events show corporate greed at its worst. But there is more. To attempt to minimize the
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`perceived impact of its conduct, Syngenta actively misled farmers, industry participants and others about
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`the importance of the Chinese market, the timing and substance of its application for approval in China,
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`the timing of when China was likely to approve MIR162, its ability to “channel” Viptera® to non-
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`Chinese markets and otherwise contain the infiltration of Viptera® into the U.S. corn supply and other
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`issues described below. In fact, even though it represented to the USDA and the public that “there
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`should be no effects on the U.S. maize export market” from deregulation and that it would impose
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`stewardship and channeling requirements to steer Viptera® corn away from export markets that had not
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`approved it, Syngenta did not follow through in any meaningful way on this commitment. Just the
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`opposite. When one company – Bunge North America, Inc. (“Bunge”) – tried to minimize the risk that
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`Viptera® would be found in shipments to China by refusing to accept it, Syngenta sued Bunge in an
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`effort to force it to take Viptera®. Syngenta was far more concerned about the impact on its business
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`than it was about the loss of an important export market for the corn industry.
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`Under the basic laws of supply and demand, when there is less demand for a product, the price is
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`lower than it otherwise would be. China was a large and growing export market, and was predicted by
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`the USDA to be our largest export market for corn by 2020. China was also a large and growing market
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`for DDGS, which are also sold by many Non-Producers. The loss of these markets has caused
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`enormous economic harm to U.S. corn Producers and Non-Producers, and that harm is continuing to
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`grow. While China finally approved MIR162 in December 2014, it has not approved Event 5307. U.S.
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`corn exports to China have not yet begun to recover, and it remains to be seen whether they will ever
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`regain the levels they would have attained but for the embargo.
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`Those injured by Syngenta’s conduct fall into two groups: (a) Producers (farmers and others
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`actually involved in the production of U.S. corn) who grow corn and sell it to other market participants;
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`and (b) all of the other Non-Producer market participants affected by the drop in corn prices and/or the
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`rejection of U.S. corn and corn by-products in foreign markets because of the presence of MIR162. This
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`Complaint sets forth the claims of DeLong, a Non-Producer. With this Complaint, Plaintiff seeks
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`compensation for losses it has suffered as a result of Syngenta’s irresponsible conduct, and punitive
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`damages for Syngenta’s reprehensible and outrageous behavior.
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`JURISDICTION AND VENUE
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`This Court has jurisdiction over this case under 28 U.S.C. § 1331, 28 U.S.C. §
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`1.
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`1332(a)(1)-(3), and 15 U.S.C. § 1121(a) in that claims are asserted under § 43(a) of the Lanham Act, 15
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`U.S.C. § 1125(a).
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`2.
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`In the further alternative, this Court has supplemental jurisdiction over this case under 28
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`U.S.C. § 1367(a).
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`3.
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`Venue is proper in the Western District of Wisconsin pursuant to 28 U.S.C. § 1391(b)(2)
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`because DeLong suffered damages in this District due to Defendants’ conduct. Additionally, venue is
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`also proper the Western District of Wisconsin pursuant to 28 U.S.C. § 1391(b)(2) because Defendants
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`have marketed, sold, or otherwise disseminated, and continue to market, sell, or otherwise disseminate
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`Viptera® and Duracade™ corn in this District.
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`PARTIES
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`4.
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`Plaintiff DeLong is a Wisconsin corporation with its corporate headquarters and principal
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`place of business at 513 Front St., PO Box 552, Clinton, Wisconsin 53525, located in Rock County,
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`Wisconsin. Over the years, DeLong developed an extensive network of grain elevators and grain
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`handling and processing facilities (including loading facilities, rail terminals, river terminals and port
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`elevators) and transportation assets (including trucks, rail cars, containers and barges) primarily in the
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`Midwest that it uses to buy, store, clean, process, and transport agricultural commodities, including corn,
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`that DeLong purchases directly from farmers. DeLong exports significant amounts of corn (and beans)
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`to Asia. DeLong also developed a significant business in “DDGs” from ethanol plants that it sells for
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`livestock feed. DeLong became one of the largest exporters of DDGs to China as China’s growing
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`population and burgeoning middle class created significant demand for corn and corn by-products
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`including DDGs (due to pork consumption skyrocketing in China in the last 10 years). DeLong made
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`substantial investments to support its growing export business to China.
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`5.
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`Syngenta AG is a corporation organized and existing under the laws of Switzerland with
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`its principal place of business at Schwarzwaldallee 215, 4058 Basel-Stadt, Switzerland. Syngenta AG is
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`a publicly traded company on the Swiss stock exchange. American Depository Receipts for Syngenta
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`AG are traded on the New York Stock Exchange. Syngenta AG was formed in 2000 as a result of the
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`merger of Novartis Agribusiness and Zeneca Agrochemicals and is the only publicly traded company
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`among the various Syngenta entities named as defendants in this case. Service of Syngenta AG with
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`process under Fed. R. Civ. P. 4(h)(2) and 4(f)(1), and in accordance with the Hague Convention on the
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`Service Abroad of Judicial and Extrajudicial Documents in Civil or Commercial Matters, may be made
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`by forwarding two copies of the citation and the Complaint in English, along with two copies of the
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`citation and the Complaint translated into German, to: Appellationsgericht, Basal-Stat, Baumleingasse1,
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`4051 Basel, Switzerland. This Complaint may be served upon Syngenta AG under Fed. R. Civ. P.
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`5(b)(2)(C) by mailing a copy of it to Syngenta AG at its principal place of business noted above.
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`6.
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`Crop Protection AG is a corporation organized and existing under the laws of
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`Switzerland with its principal place of business at Schwarzwaldallee 215, 4058 Basel-Stadt,
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`Switzerland. Service of Crop Protection AG with process under Fed. R. Civ. P. 4(h)(2) and 4(f)(1), and
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`in accordance with the Hague Convention on the Service Abroad of Judicial and Extrajudicial
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`Documents in Civil or Commercial Matters, may be made by forwarding two copies of the citation and
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`the Complaint in English, along with two copies of the citation and the Complaint translated into
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`German, to: Appellationsgericht, Basal-Stat, Baumleingasse1, 4051 Basel, Switzerland. This
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`Complaint may be served upon Crop Protection AG under Fed. R. Civ. P. 5(b)(2)(C) by mailing a copy
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`of it to Crop Protection AG at its principal place of business noted above.
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`7.
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`Syngenta Corporation is a Delaware corporation with a principal place of business at
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`3411 Silverside Road #100, Wilmington, Delaware 19810-4812. Syngenta Corp is a subsidiary of
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`Syngenta AG. Syngenta Corp. does not have a registered agent in the State of Wisconsin and may be
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`served with process under Rule 4(h)(1)(A) and (B) by sending by registered or certified mail the citation
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`and this Complaint to: Cheryl Quain (or successor), Corporate Secretary, Syngenta Corporation, 3411
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`Silverside Road, Suite 100, Shipley Building, Wilmington, Delaware 19810, and The Corporation Trust
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`Company, Corporation Trust Center, 1209 Orange Street, Wilmington, Delaware 19801.
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`8.
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`Crop Protection, LLC is a limited liability company organized and operating under the
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`laws of the State of Delaware with its principal place of business at 410 Swing Road, Greensboro, North
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`Carolina 27409-2012. Crop Protection, LLC may be served under Fed. R. Civ. P. 4(h)(1)(A) by and
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`through its registered agent, C T Corporation System, 301 S. Bedford St. Suite 1, Madison, Wisconsin
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`53703.
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`9.
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`Syngenta Seeds LLC (“Syngenta Seeds”), formerly a Delaware corporation with a
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`principal place of business at 11055 Wayzata Boulevard, Minnetonka, Minnesota 55305-1526, is now a
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`Delaware limited liability company with Syngenta Corp. as its sole member. Syngenta Seeds is a direct
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`subsidiary of Syngenta Corp. It may be served under Fed. R. Civ. P. 4(h)(1)(A) by and through its
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`registered agent, C T Corporation System, 301 S. Bedford St. Suite 1, Madison, Wisconsin 53703.
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`Syngenta Seeds has described itself in its Complaint filed in Syngenta Seeds, Inc. v. Bunge North
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`America, Inc., No. 5:11-cv-04074-MWB, United States District Court, Northern District of Iowa
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`(“Bunge” or “Syngenta v. Bunge”), as
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`a leading agribusiness company committed to sustainable agriculture through research
`and technology. Syngenta is, among other things, in the commercial seed business. It
`develops, produces, and sells, through dealers and distributors or directly to growers, a
`wide range of agricultural products, including corn and soybean seed exhibiting useful
`traits that have been developed with the techniques of modern biotechnology. The seed
`products are then grown and harvested as raw materials for the production of biofuels or
`grain for livestock feed; or are milled and processed for food products.
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`Among Syngenta Seeds’ products which it has sold in the State of Wisconsin, and elsewhere, including
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`states in which DeLong has operations, are the Agrisure Viptera® and Agrisure Duracade™ corn
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`seeds. These seeds express, or contain, genetically engineered traits which confer resistance to insects.
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`10.
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`Syngenta Biotech, formerly a corporation organized and existing under the laws of the
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`State of Delaware with its principal place of business located at P.O. Box 12257, 3054 East Cornwallis
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`Road, Research Triangle Park, North Carolina 27709-2257, has now merged into Crop Protection, LLC,
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`with Crop Protection, LLC as the surviving entity. Syngenta Biotech, prior to its merger with Crop
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`Protection, LLC, was a subsidiary of Syngenta Seeds and traces its operations back to CIBA-Geigy
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`Corporation, a legacy company of Syngenta. Syngenta Biotech may be served under Fed. R. Civ. P.
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`4(h)(1)(A) by and through its registered agent, C T Corporation System, 301 S. Bedford St. Suite 1,
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`Madison, Wisconsin 53703.
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`11.
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`Syngenta AG wholly owns, directly or indirectly, each of Crop Protection AG,
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`Syngenta Corp., Crop Protection LLC, Syngenta Biotech and Syngenta Seeds.
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`12.
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`Syngenta AG represents itself as a global company. According to Syngenta’s own
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`website, Syngenta AG’s Board of Directors “has full and effective control of the company and holds
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`ultimate responsibility for the company strategy.”
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`13.
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`One or more members of Syngenta AG’s Board of Directors or Executive Committee
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`established by the Board of Directors also serve as member(s) of the Board of Directors of Crop
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`Protection AG, Syngenta Corp., Crop Protection LLC, Syngenta Biotech and/or Syngenta Seeds.
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`14.
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`Furthermore, Syngenta AG’s Executive Committee formulates and coordinates the
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`global strategy for Syngenta businesses, and maintains central corporate policies requiring Syngenta
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`subsidiaries, including those named as Defendants herein, under the general guidance of the Syngenta
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`group control.
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`15.
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`Employees of the Syngenta group as a whole maintain reporting relationships that are
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`not defined by legal, corporate relationships, but in fact cross those corporate lines. For example,
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`Crop Protection AG maintains two separate product lines – Seeds and Crop Protection – that cross the
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`Defendants’ separate legal, corporate existences.
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`16.
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`The Defendant subsidiaries are subject to additional oversight that requires them to
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`seek approval for certain decisions from higher levels within the functional reporting structure –
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`including in some instances Syngenta AG. Appointments of senior management personnel for the
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`Defendant subsidiaries also may require, in certain instances, approval from individuals or governing
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`bodies that are higher than each subsidiary’s respective board of directors.
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`17. Moreover, Syngenta AG and Syngenta Crop Protection AG management were intimately
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`involved in, and in some instances directed, decisions concerning the commercialization of Viptera®
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`without Chinese approval.
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`18.
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`Also, Syngenta AG maintains a central global finance function that governs all
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`Defendants. Thus, the Defendant subsidiaries do not function independently but under the Syngenta
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`AG umbrella.
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`19.
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`In addition, Syngenta entities regularly refer to themselves as “Syngenta,” with no
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`further description.
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`20.
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`Thus, the respective jurisdictional contacts of Crop Protection AG, Syngenta Corp.,
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`Crop Protection LLC, Syngenta Biotech and Syngenta Seeds in the forum state(s) are attributable to
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`Syngenta AG because of the unusually high degree of control Syngenta AG exercises over these
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`subsidiaries. See, e.g., City of Greenville v. Syngenta Crop Protection, Inc. et al., 830 F. Supp. 2d 550
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`(S.D. Ill. 2011).
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`21.
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`In addition, upon information and belief, the Defendants acted in concert pursuant to
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`agreements or other arrangements to act in a collective manner and/or as joint venturers regarding the
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`actions and events made the subject of this Complaint. All Defendants are therefore jointly and
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`severally liable for the acts for which the Plaintiff makes complaint.
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`FACTUAL ALLEGATIONS
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`22.
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`Biotechnology firms such as Syngenta develop and obtain patents on their bio-engineered
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`products, in this instance seeds. These products are also referred to as genetically-modified organisms,
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`or “GMOs.” A patent gives the biotechnology firm the exclusive right to sell its bio-engineered
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`products; however, those patents eventually expire. Biotechnology seed firms therefore have an
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`economic incentive to “commercialize” (i.e. bring their products to market for planting and harvest) as
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`soon as possible after filing a patent application in order to maximize profitability.
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`23.
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`According to Grant Ozipko, the goal set by Syngenta’s senior leadership (including
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`Charles Lee, David Morgan, Steve Ligen and/or Diane Mayhart) was to achieve 9.5% market share for
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`MIR162 by 2014. See Grant Ozipko Deposition (10/19/12) (Bunge) at 72-73. Syngenta was concerned
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`with “commercialization as soon as possible.” See MIR162H-I Stage gate progression review dated
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`December 16, 2009.
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`24.
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`But premature commercialization poses well-known and significant risks of harm to
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`farmers and industry participants if bio-engineered commodity products are commercialized before they
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`are approved by major importing nations. Certain importing nations, such as China, have a “zero
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`tolerance” policy and will reject grain and/or grain product imports from the U.S. upon detecting the
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`presence of even trace amounts of an unapproved bio-engineered genetic trait in U.S. grain or grain
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`product shipments. This was well known by participants in the biotechnology industry, including
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`Syngenta, before, but at least by, 2007.
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`25.
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`Syngenta commercialized MIR162 – and Event 5307 – despite clear risk of harm to its
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`stakeholders (including the Plaintiff), Syngenta’s knowledge of that risk, and Syngenta’s own professed
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`commitment to responsible management.
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`26. Moreover, Syngenta commercialized MIR162 by consistently misrepresenting the
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`importance and status of China’s approval and without adequate systems in place to isolate or channel
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`MIR162, virtually assuring that MIR162 would contaminate the U.S. corn supply, as set out below.
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`Recognized Risks Of Irresponsible Commercialization
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`27.
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`As recognized within the industry, and by Syngenta, the harm threatened by irresponsible
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`commercialization is very real.
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`28.
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`“There have been a number of high-profile cases involving genetically modified varieties
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`. . . and disruption of international shipments of commodity grains such as corn, wheat, and rice.”
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`http://www.syngentafoundation.org/index.cfm?pageID=703.
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`29.
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`High profile examples of irresponsible commercialization of bio-engineered seeds
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`include “StarLink” bio-engineered corn that contaminated the U.S. corn supply in 2000 and thereby
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`disrupted international trade, causing loss to farmers and other industry participants. In re StarLink
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`Corn Products Liability Litigation, 212 F. Supp. 2d 828 (N.D. Ill. 2002).
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`30.
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`In 2006, bio-engineered rice contaminated the U.S. rice supply, again disrupting trade
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`and causing massive damages to U.S. rice farmers and other industry participants. See, e.g., In re
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`Genetically Modified Rice Litig., 666 F. Supp. 2d 1004 (E.D. Mo. 2009); Bayer CropScience LP v.
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`Schafer, 2011 Ark. 518, 385 S.W.3d 822, 832 (Ark. 2011).
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`31.
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`In addition to being aware of these and other well-publicized incidents and lawsuits at the
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`time Syngenta decided to commercialize MIR162, Syngenta had (and has been) continuously warned by
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`stakeholders about the importance of, and need for, responsible commercialization.
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`32.
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`For example, when Syngenta commercialized MIR604 (Agrisure® RW) in 2007, the
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`National Grain and Feed Association (“NGFA”) (of which Syngenta is a member) and the North
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`American Export Grain Association (“NAEGA”) warned against an “‘ill-conceived’ plan to
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`commercialize” Syngenta’s Agrisure biotechnology-enhanced corn as endangering U.S. corn and corn-
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`product exports since it had not obtained regulatory approval for food and feed use in Japan and other
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`U.S. export markets. Houin, “Feed and grain organizations warn growers of limited export markets,”
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`Farm World (4/25/2007).
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`33.
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`The International Grain Trade Coalition also chastised Syngenta, stating that Syngenta
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`“did not respect the responsibility of importing governments to perform necessary risk assessments as
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`demanded by their legislation,” that the introduction of Agrisure® RW “was not done in an open
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`transparent manner,” and that Syngenta “did not complete authorization in major international markets
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`possessing scientifically sound approval systems prior to commercialization.” Letter from International
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`Grain Trade Coalition to Michael Pragnell, CEO Syngenta dated April 18, 2007 at 2. The International
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`Grain Trade Coalition further stated that Syngenta’s conduct “[e]xposed downstream members of the
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`value chain including producers, handlers, exporters, importers, food processors and distributors to
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`significant liability as currently all countries employ a zero threshold policy for an event not authorized
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`by the importing country” and strongly urged Syngenta to “reverse immediately its decision to
`
`commercialize Agrisure RW at this time.” Id.
`
`34.
`
`The Biotechnology Industry Organization (“BIO”) is the world’s largest biotechnology
`
`trade association, of which, on information and belief, Syngenta is or was a member. BIO has expressly
`
`recognized that “[a]synchronous authorizations combined with importing countries maintaining ‘zero
`
`tolerance’ for recombinant-DNA products not yet authorized results in the potential for major trade
`
`disruptions.” BIO, Product Launch Stewardship Policy, May 21, 2007, at Annex 1 Introduction; see also
`
`BIO Product Launch Stewardship,” December 10, 2009, at Annex 1 Introduction (same); BIO
`
`“Stewardship: Actions to be Taken Prior to Launching Special Traits,” October 4, 2010, at Annex 1
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`Case 2:17-cv-02614-JWL-JPO Document 1 Filed 10/11/17 Page 14 of 116
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`Introduction (same); BIO “Product Launch Stewardship: Food and Agriculture Section,” November 27,
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`2012, at Annex 1 Introduction (same).
`
`35.
`
`As stated in BIO’s “Product Stewardship Policy” dated December 10, 2009:
`
`introduction of biotechnology-derived plant
`the commercial
`Since
`products in 1996, an increasing number of biotechnology-derived plant
`products intended for food or feed use are authorized for commercial
`production
`in many countries
`throughout
`the world; however,
`authorizations in importing countries vary depending on the timing of
`submissions for import authorization as well as the duration of the
`authorization process in each country. As a consequence of these
`asynchronous authorizations, low levels of recombinant-DNA plant
`materials that have completed full safety assessments in accordance with
`national and international standards in one or more countries may, on
`occasion, be present in food or feed in countries in which the authorization
`process of the relevant recombinant-DNA plant material has not been
`completed.
`importing countries
`Asynchronous authorizations combined with
`maintaining ‘zero tolerance’ for recombinant-DNA products not yet
`authorized results in the potential for major trade disruptions.
`
`
`http://www.bio.org/sites/default/files/Product_Launch_Stewarship_12_10_09.pdf.
`
`Recognized Stewardship Obligation
`
`36.
`
`The risks of premature commercialization are well-recognized within the industry and as
`
`a result agricultural biotechnology organizations, including CropLife International (of which Syngenta is
`
`a member) and BIO have developed stewardship standards under which bio-technology firms refrain
`
`from commercializing their products before those products are approved by importing nations.
`
`37.
`
`The very genesis of BIO’s Product Launch Stewardship Policy in 2007 was Syngenta’s
`
`own launch of MIR604 without Japanese import approval. See John Bernens Deposition (11/2/12)
`
`(Syngenta Seeds, Inc. v. Bunge North America, Inc., No. 5:11-cv-04074-MWB (N.D. Iowa Aug. 22,
`
`2011)) at 110-113; see also Email from Sarah Hull to Jane Backmann and Anne Burt dated February 19,
`
`2008 (“While I know we will be ready to sell MIR162 in the US in 2009, it seems we won’t have the
`
`stacks approved in Japan to fully launch the product without managing some trade implications. This is
`14
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`4220914.8
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`
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`Case 2:17-cv-02614-JWL-JPO Document 1 Filed 10/11/17 Page 15 of 116
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`where grain traders were so upset with the [Agrisure] RW launch. We commercialized without having
`
`Japan approval prior to planting. That in turn spawned the BIO policy.”).
`
`38.
`
`Syngenta has, since at least 2007, represented that it is “committed to the principles of
`
`good stewardship, which are exemplified through the responsible management of [its] products across
`
`their lifecycle [including] commercialization” and its support for BIO’s Product Launch Stewardship
`
`policies. See Bio Product Launch Policy, Syngenta Implementation Principles (Nov. 2007)
`
`http://www.syngentabiotech.com/biopolicy.aspx. On information and belief, Syngenta’s Jeff Cox
`
`expressly indicated Syngenta’s support for this policy and pledged that “we will implement it with
`
`Syngenta.”
`
`39.
`
`Under the BIO stewardship policy, developers like Syngenta should meet applicable
`
`regulatory requirements in key markets prior to commercialization. See BIO Product Launch
`
`Stewardship, December 10, 2009, at 4.
`
`40.
`
`Under the BIO policy, developers also should:
`
`Conduct a market and trade assessment to identify key import markets,
`including those with functioning regulatory systems, prior to the
`commercialization of any new biotechnology product (crop by event) in
`any country of commercial launch. In that market and trade assessment,
`consult at an early stage with the value chain for the specific crop.
`Manage the product’s introductions so that choice of production
`methods
`(coexistence) and markets
`(e.g.,
`specialty,
`identity
`preservation, and global) for that crop are available and preserved.
`Id. (emphasis added).
`
`Under the BIO policy in 2009, key markets included “at minimum” the United States,
`
`41.
`
`Canada, and Japan. Id. (emphasis added).
`
`42.
`
`For purposes of the BIO policy, “commercialization” means the first planting of seed for
`
`the production of a crop or crop product. See BIO Product Launch Stewardship, December 10, 2009, at
`
`4 n.4. See also Email from Sarah Hull to Jane Bachmann and Anne Burt dated February 19, 2008
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`(commercialization is defined in BIO policy as the first planting of seed sold into commerce for the
`
`production of a crop).
`
`43.
`
`BIO policies are minimum standards of responsible behavior. BIO expressly states that
`
`its policy “does not limit the implementation of additional measures designed to facilitate adoption and
`
`use of [commodity crop] products and to prevent disruption of . . . the trading of the commodity.” BIO
`
`Product Launch Stewardship, December 10, 2009, at 4.
`
`44.
`
`Another biotechnology industry association, Excellence Through Stewardship, advocates
`
`similar
`
`standards
`
`through
`
`its
`
`“Product
`
`Launch
`
`Stewardship
`
`Guide.”
`
`http://excellencethroughstewardship.org/wp-content/uploads/Approved-Product-Launch-Stewardship-
`
`Guide-Revised-07-22-10.pdf. Syngenta is a “founding member” of Excellence Through Stewardship.
`
`www.syngentabiotech.com/biostewardship.aspx.
`
`45.
`
`Biotechnology industry groups are not alone in recognizing the importance of
`
`stewardship. The National Grain and Feed Association’s Policy on Agriculture Biotechnology provides:
`
`The NGFA supports agricultural biotechnology and other scientific
`advancements that promote safe and abundant food and feed supply.
`However, the NGFA believes biotech-enhanced traits should be
`commercialized only after achieving broad, deep consumer
`ac