MEMORANDUM OPINION AND ORDER
Abbott Laboratories, Inc. (“Abbott”) filed a breach of contract action against BioValve Technologies, Inc. (“BioValve”) on April 16, 2007. BioValve moved to dismiss Abbott’s Complaint pursuant to Federal Rule of Civil Procedure 12(b)(2) on August 27, 2007, contending that the court lacks personal jurisdiction over it. For the reasons explained below, the court denies BioValve’s motion.
FACTUAL BACKGROUND
The court draws the factual background of this case primarily from the parties’ affidavits.
See Purdue Research Found, v. Sanofi-Synthelabo, S.A,
Abbott is an Illinois corporation with its principal place of business in Abbott Park, Illinois. (Compl. ¶ I.A.) BioValve is a Delaware corporation with its principal place of business in Shrewsbury, Massachusetts. (ComplV I.B.) There is no dispute that — as BioValve’s President and CEO Robert Gonnelli has attested — BioValve has no offices in Illinois, no manufacturing facilities in Illinois, no employees employed in Illinois, no Illinois bank account, and no Illinois telephone number. (Docket Entry No. 17, Gonnelli Aff. ¶¶ 1, 3.) BioValve is not licensed to conduct business in Illinois and does not regularly conduct business in Illinois. (Id. ¶ 3.) It does not solicit business or advertise in Illinois. (Id.) Aside from this litigation, BioValve has never been named as a party to an action in Illinois. (Id. ¶ 5.) The parties therefore dispute whether this court has jurisdiction to adjudicate Abbott’s breach of contract claim against BioValve.
Apparently, BioValve’s only contact with the state of Illinois is related to the contract at issue in this lawsuit. Early in 2005, Deborah Davis — Abbott’s Program Manager of Global Pharmaceutical Research and Development (“GPRD”), Process Research and Process Development— identified several potential Abbott customers in the Research Triangle Park area of North Carolina. (Docket Entry No. 24, Davis Aff. ¶¶ 1, 4.) One of these potential customers was DarPharma, Inc., a virtual company with no research and development facilities of its own. (Id. ¶¶ 4-5.) Prabha Fernandes, a former Abbott employee, headed DarPharma. (Id. ¶ 5.) Despite DarPharma’s lack of research and development facilities, Davis “was told that DarPharma was developing a compound known as DAR-0100,” which was structurally similar to a previous Abbott development product. (Id. ¶ 6.) David E. Nichols, a Purdue University professor, developed the molecule that underlies DAR-100. (Docket Entry No. 28, Gonnelli Supp. Aff. ¶ 2.) BioValve licenses the DAR-100 molecule, but it pays the licensing fees pursuant to a licensing agreement that originally ran between Purdue University and DarP-harma rather than directly to Nichols. (Id. ¶ 3.)
After receiving additional information about DAR-0100, on March 31, Abbott submitted a proposal to Fernandes, in which Abbott proposed to prepare one kilogram of DAR-0100. (Davis Aff. ¶ 7.) In April 2005, Fernandes told Davis that
As explained above, BioValve was to pay for Abbott’s work on the DAR-0100 project. On July 22, 2005, Edward O’Keefe— an Abbott Senior Financial Analyst supporting the GPRD Division — called and emailed BioValve to request a purchase order. (Docket Entry No. 23, O’Keefe Aff. ¶¶ 1, 4.) On July 29, Michele Carter — a BioValve employee — sent O’Keefe a purchase order by e-mail, which O’Keefe deemed consistent with “the proposal.” (O’Keefe Aff. ¶ 5.) Bob Gonnelli and Jim Patzke approved the Purchase Order, which is for “Process Development & Manufacture of Chiral API (1 kg)” at a unit price of $590,000. (Ex. 1 to O’Keefe Aff., E-mail from O’Keefe to Davis of 8/1/05.) Gonnelli is BioValve’s President and CEO, while Patzke is BioValve’s Director of Quality. (Davis Aff. ¶ 11; Gonnelli Aff. ¶ 1.) For jurisdictional purposes, it is significant to note that there is no suggestion that the Purchase Order contained a choice of law provision, that the Purchase Order contained a choice of jurisdiction provision, or that BioValve has entered into any other contracts with Abbott.
Abbott has facilities, among other places, in both Illinois and Massachusetts. BioValve’s President and CEO claims that “[w]hen Biovalve first approached Abbott about producing the DAR-100A, Biovalve was well aware of the existence of Abbott’s Worcester [Massachusetts] facility.” 1 (Gonnelli Aff. ¶ 7.) Nevertheless, BioValve acknowledges that it had “no role” in selecting which Abbott facility would produce the DAR-100A. (Id. ¶ 9.) Davis’ project team began working on the DAR-0100 project in early August 2005. (Davis Aff. ¶ 13.) Abbott “unilaterally” selected its North Chicago, Illinois facility as the location for all research, development, manufacture, and storage of DAR-0100. (Gon-nelli Aff. ¶ 10; Davis Aff. ¶ 28.) Wayne Pritts and Dan Plata — both Abbott Senior Group Leaders of GPRD Process Research and Development — were members of the project group working on the syn- . thesis of DAR-0100. (Docket Entry No. 26, Pritts Aff. ¶¶ 1-4; Docket Entry No. 25, Plata Aff. ¶ 1-4.) Pritts and Plata have confirmed that all analytical method developing and testing as well as production of DAR-0100 occurred at Abbott’s North Chicago facility. (Pritts Aff. ¶ 5; Plata Aff. ¶¶ 5, 11.) Abbott’s Worcester facility was “in no manner” involved with the DAR-0100 project. (Davis Aff. ¶ 29.)
Beginning in August 2005, Abbott was in direct communication with DarPharma regarding the DAR-0100 project. Until the end of December 2005, Davis, Fernandes, and Nichols — the developer of the molecule underlying DAR-100 — conducted all communications related to the DAR-0100 project. (Davis Aff. ¶ 14.) No further
On two occasions in 2006, BioValve employees also visited the Abbott facilities in North Chicago, Illinois. Huie and Davis set up the first meeting in January 2006, with the Abbott project team, Huie, and one other BioValve representative. (Davis Aff. ¶¶ 16-17.) In an e-mail to Davis, Huie describes the purpose of the meeting as being to “review the status of the DAR 100A synthesis” and to “audit the facility and procedures and review specifications based on [Abbott’s] small batch run results.” (Ex. 1 to Davis Aff., E-mail from Huie to Davis without identifying header information.) According to his e-mail, Huie expected the meeting to last for at least five hours. (Id.) At the meeting, Plata, on behalf of Abbott, presented to' BioValve the DAR-0100 project status and proposed timeline for completion. (Plata Aff. ¶¶ 8-9.) Plata never mentioned Abbott’s Massachusetts facility, or any non-Illinois facility, during his presentation. (Id. ¶ 11) As a part of the January 2006 visit to Abbott’s Illinois facilities, on January 9, 2006, BioValve employees Patzke and Huie conducted a “customer audit” of Abbott’s North Chicago production facility and provided a detailed report. (Davis Aff. ¶ 18.) 3 Huie’s e-mail does not make clear to whom the report was provided, but Abbott asserts that it was given to Davis. (PL’s Opp. at 8.) Following the meeting, Davis and her team advised Bio-Valve employees that the project would not be complete until late April and agreed to provide BioValve with regular updates regarding the project. (Davis Aff. ¶ 19.)
BioValve’s employees made a second trip to Illinois almost three months later. On March 29, 2006, Huie, Patzke, Ron Nardi, and Dan Connors — all BioValve employees — attended a meeting with Abbott employees in Illinois. (Davis Aff. ¶¶ 11, 20.) At the March 2006 meeting, Plata reported on the progress of the project; he made no mention of any Abbott facility other than North Chicago. (Plata Aff. ¶¶ 10-11.) Pritts also participated in the meeting on Abbott’s behalf. (Pritts Aff. ¶ 9.) According to Pritts, the parties discussed and verbally agreed on “final API specifications that would be used to test and release the DAR-0100 that was being produced.”
(Id.
¶ 10;
see also
Davis Aff. ¶ 21.) In an e-mail message dated April 6, BioValve ultimately approved the specifications that the parties had dis
On April 30, 2006, Davis advised Bio-Valve employees that the synthesis of DAR-0100 was complete, though it is not clear by what means this information was communicated. (Davis Aff. ¶ 24.) At Bio-Valve’s request, the product was packaged in 100-gram portions, in amber glass bottles, and refrigerated in Abbott’s North Chicago facility. (Id. ¶ 25.) Also at Bio-Valve’s request, on May 8, 2006, Davis sent BioValve a report comparing the analytical methods used at Abbott with the “old” methods used. (Id. ¶ 28.) At the end of that month, Davis advised BioValve (though again, it is not clear by what means) that the product was tested and approved for shipment. (Id. ¶ 26.) Davis then contacted Huie by telephone and email to receive shipping information, but she never obtained the information from Huie or BioValve. (Id. ¶ 27.) According to Gonnelli, BioValve “recently” instructed Abbott to ship the first shipment of DAR-100A to BioValve’s Massachusetts facility. (Gonnelli Aff. ¶ 11.)
On June 23, 2006, O’Keefe sent an invoice to Carter at BioValve, which requested payment of $590,000 for “API GMP with Certificate of Analysis” and $96,777 for “Raw/Starting Materials.” (Ex. 3 to O’Keefe Aff., Invoice dated 6/23/06.) The invoice does not reference DAR-0100 by name, but the parties agree that the only purchase order or contract between Bio-Valve and Abbott relates to the DAR-0100 project. This June 23 invoice, however, was later modified. After negotiations with Gonnelli, on September 26, 2006, O’Keefe sent a replacement invoice to Carter, which requested payment of $590,000 for API GMP with Certificate of Analysis but requested no payment for starting materials. (O’Keefe Aff. ¶¶ 9-10; Ex 2 to O’Keefe Aff., Invoice dated 9/26/06.) According to BioValve, on June 20, 2007, the parties reached a settlement agreement (though it is not clear where the parties negotiated or signed the agreement) resolving the outstanding payments due to Abbott. (Def.’s Mem. at 3 n. 1.) BioValve made the first payment due under the parties’ settlement agreement, for an amount not disclosed to the court, but it has run into financing difficulties in connection with the second payment, thus prompting this litigation. (Id.)
DISCUSSION
I. Rule 12(b)(2)
Rule 12(b)(2) permits a court to dismiss a complaint for “lack of personal jurisdiction.” To successfully oppose a Rule 12(b)(2) motion, a plaintiff bears the burden of demonstrating that the court has personal jurisdiction over the defendant.
RAR, Inc. v. Turner Diesel, Ltd.,
II. Personal Jurisdiction
A. Legal Standard
As a federal district court exercising diversity jurisdiction, this court has personal jurisdiction over BioValve only if an Illinois state court would have personal jurisdiction.
RAR, Inc.,
The Supreme Court has explained that, to satisfy the federal due process inquiry, the defendant must have “minimum contacts” with the forum state “such that the maintenance of the suit does not offend traditional notions of fair play and substantial justice.”
Int’l Shoe Co. v. Wash.,
In addition, the Supreme Court has distinguished between “general” jurisdiction and “specific” jurisdiction.
Hyatt Int'l,
B. BioValve’s Contacts with Illinois
As a threshold matter, the court agrees with BioValve that it is not subject to personal jurisdiction in Illinois merely because it entered into a contract with an Illinois resident.
See Prime Leasing, Inc. v. Jackson-Madison Cty. Gen. Hosp. Dist.,
No. 91 C 5726,
1. Communications
BioValve argues that its telephone and e-mail communications with Abbott do not merit an exercise of personal jurisdiction. These communications, however, were significant and occurred over a long period of time. BioValve never contests that it reviewed and proposed changes to the proposal Abbott originally sent to DarPharma in the spring of 2005. Although neither party makes clear where the review or revisions occurred, these activities demonstrate that BioValve was at least in indirect contact with Abbott regarding the project in 2005. In addition, in 2005, Bio-Valve communicated directly with Abbott regarding the Purchase Order. BioValve affirmatively acknowledges that, in January 2006, after Fernandes resigned, Abbott and BioValve began communicating directly and substantively regarding the project. (Def.’s Reply at 2.) Specifically, Davis and Huie communicated by phone and e-mail to set up the January 2006 meeting and audit. (Davis Aff. ¶¶ 16-17.)
Isolated telephone and e-mail communications, alone, may not be a basis for asserting personal jurisdiction over BioValve.
See Delcon, Inc. v. Robert McMullan & Son, Inc.,
No. 85 C 4220,
2. Physical Presence
Moreover, there is no dispute that Bio-Valve employees visited the Abbott facility in North Chicago, Illinois on two occasions.
(See
Gonnelli Aff. ¶ 10.) Arguing that these two visits should not lead the court to exercise personal jurisdiction, BioValve points the court to three cases from this district in which a non-resident’s trips to Illinois were deemed insufficient to establish personal jurisdiction of a district court. In the first case, the non-resident defendant made two visits to Illinois. The defendant’s first visit — -to an art gallery with whom he later entered a contractual relationship — was made while he was in Illinois for other purposes, and the parties did not negotiate during his visit.
Maurice,
Similarly, in the second case BioValve cites,
Delcon,
the non-resident visited Illinois to negotiate a contract, but those negotiations were probably non-substantial and, in any case, resulted only in the nonresident making an offer that the plaintiff rejected.
Neither doctrine is at issue in this case. BioValve’s visits to Illinois were substantive, directly related to performance under the contract (rather than undertaken because of artistic curiosity), and successfully determined project specifications: First, the BioValve employees clearly came to Illinois in connection with the DAR-0100 project and performed substantial work related to it. In January 2006, Huie and Patzke visited Abbott, in Huie’s words, to “review the status of the DAR 100A synthesis” and to “audit the facility and procedures and review specifications based on [Abbott’s] small batch run results.” (Email from Huie to Davis without identifying header information.) Huie and Patzke intended to meet with Abbott for at least five hours; Huie suggested that they meet on January 9 from 12 p.m.-5 p.m., and for an additional three hours on January 10, if necessary. (Id.) While Huie’s e-mail suggests that the BioValve employees had other business purposes for visiting Illinois, the trip to Abbott served a substantial purpose related to the DAR-0100 project. Significantly, during this visit, Huie and Patzke undertook serious investigation and discussion related to the project’s performance, status, and timeline with the Abbott team. They also conducted the requested “customer audit” of Abbott’s North Chicago facility, and prepared a de-tañed report. (Davis. Aff. ¶ 18.) Unlike the defendant’s first visit in the Maurice case, Huie’s and Patzke’s trip to Illinois was directly related to Abbott’s performance under the contract.
In March 2006, Huie and Patzke traveled to Illinois again, this time with Nardi and Connors. (Davis Aff. 1120.) Bio-Valve’s president and CEO attested that the meeting was necessary because Abbott was having difficulty producing DAR-100A, and BioValve employees came to the facility to provide assistance in order “to ensure that the final product would still meet Biovalve’s requirements.” (Gonnelli Aff. ¶ 10.) During the March 2006 meeting, Abbott and BioValve “discussed and agreed upon the final specifications on
Wisconsin Electrical,
a case not cited by the parties, is instructive.
Wisc. Elec. Mfg. Co. v. Pennant Prods., Inc.,
BioValve contends that cases in which a defendant solicits a contract are not comparable to cases in which the defendant merely accepts the solicitation. But courts have rejected this distinction as dispositive where a non-resident defendant visited the forum state in connection with contract performance.
United States Gypsum Co. v. All Tank Sales & Supply Co.,
Of course, physical presence in Illinois is neither necessary nor sufficient to subject a non-resident to personal jurisdiction. Wi
sc. Elec.,
3. Regular Business Connections
BioValve urges that it was not conducting regular business in Illinois. In this case, however, only specific jurisdiction is at issue; thus, the court “only analyzes those contacts from which the cause of action arises.”
Edelson,
C. Fairness
Finally, a due process inquiry also requires considering the equities of exercising personal jurisdiction. When doing so, Illinois courts treat active purchasers and passive purchasers differently.
Ruprecht Co. v. Sysco Food Servs. of Seattle, Inc.,
A passive purchaser “merely places an order” for goods, accepting the terms proposed by the seller, and is not typically subject to personal jurisdiction.
Id.
at 121,
CONCLUSION
For the reasons explained above, Defendant’s motion to dismiss (14) is denied.
Notes
. As it is unclear what difference, if any, there is between DAR-0100 and DAR-0100A, the court assumes that any difference between the compounds is insignificant in this context.
. According to Gonnelli, Nichols' role was to offer suggestions to overcome the difficulties Abbott had in synthesizing the DAR-100 molecule. (Gonnelli Supp. Aff. ¶ 5.) There is a dispute as to whether Nichols was a consultant to BioValve in connection with this project. (Compare Davis Aff. ¶ 14 (Nichols was a consultant to BioValve on the project) with Gonnelli Supp. Aff. ¶ 4 (Nichols was never a paid consultant to BioValve).) While the court may resolve all disputes of fact in Abbott’s favor in ruling on a Rule 12(b)(2) motion to dismiss for lack of personal jurisdiction, the court need not resolve the dispute to decide this motion and therefore will for these purposes assume that Nichols was not a paid employee, contractor, or consultant for Bio-Valve.
. Davis’ and Plata's affidavits list the date of the audit as January 9, 2005, but given the chronology of the events, the court assumes that this was a typographical error.
