Auxilium definition

Auxilium means Auxilium Pharmaceuticals, Inc., a corporation organized and existing under the laws of Delaware.
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Auxilium shall have the meaning ascribed to it in the Preamble.
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Auxilium shall have the meaning ascribed to it in the Recitals.
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Examples of Auxilium in a sentence

  • All notices and other communications required or permitted under this Agreement or necessary or convenient in connection herewith shall be in writing and shall be deemed to have been given when hand delivered or mailed by registered or certified mail, as follows (provided that notice of change of address shall be deemed given only when received): If to the Company, to: Auxilium Pharmaceuticals, Inc.

  • Auxilium also has rights to pursue additional indications for XIAFLEX.

  • A bond is a contract between the officer and the government of Swaziland to bind officers to work for government upon completion.

  • This Separation Agreement and General Release (the “Agreement and Release”) is being entered into by and between Auxilium Pharmaceuticals, Inc.

  • All notices and other communications required or permitted under this Agreement or necessary or convenient in connection herewith shall be in writing (including electronic writing via email) and shall be deemed to have been given when transmitted electronically via email, hand delivered or mailed by registered or certified mail, as follows (provided that notice of change of address shall be deemed given only when received): If to the Company, to: Auxilium Pharmaceuticals, Inc.

  • Our first product formulated CPE-215 with Testosterone, and is licensed to Auxilium Pharmaceuticals, Inc., who is currently marketing it as Testim®, a gel for testosterone replacement therapy.

  • Since 2003, Auxilium has sold Testim to pharmaceutical wholesalers and chain drug stores, which have the right to return purchased product prior to the units being dispensed through patient prescriptions.

  • First, Auxilium notes that Testim was the drug administered in the TOM trial and that the FDA's conclusion that the trial did not support an association between TRT use cardiovascular risk is clear evidence that the FDA would have rejected a strengthened cardiovascular warning label for Testim in particular.

  • Similarly, although plaintiffs contend that Auxilium tried to capitalize on, and complement, the marketing campaigns of other companies such as AbbVie, at some point testimony and evidence about other companies' advertisements would carry with it a significant risk of unfair prejudice to Auxilium.

  • Id. Auxilium argues that the Court should grant summary judgment on Holtsclaw's design-defect claim, not because of comment (k), but because Holtsclaw has failed to identify any defect in Testim's design.Auxilium is correct that Holtsclaw has not identified any defect that is attributable solely to Testim's design.


More Definitions of Auxilium

Auxilium has the meaning set forth in the introductory paragraph.
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Related to Auxilium

  • Novartis shall have the meaning set forth in the Preamble.

  • Pfizer shall have the meaning set forth in the preamble.

  • BMS means the Company, all related companies, affiliates, subsidiaries, parents, successors, assigns and all organizations acquired by the foregoing.

  • Merck has the meaning set forth in the preamble.

  • GSK will have the meaning set forth in the Preamble.

  • Elan means Elan Corp and its Affiliates.

  • Raptor means all birds of the orders Falconiformes and Strigiformes, commonly called falcons,

  • CTI means CTI Logistics Limited (ABN 69 008 778 925) and/or any Affiliate of CTI Logistics Limited as the case may be, which performs all or any of the Services.

  • ISIS means the department’s individualized services information system.

  • Shire means Shire of Augusta Margaret River

  • Lilly has the meaning set forth in the Preamble.

  • ONYX means Onyx Acceptance Corporation, and its successors.

  • ANI means automatic number identification.

  • NPS means nominal pipe size.

  • SPI means the information categories listed at Tex. Bus. & Com. Code § 521.002(a)(2).

  • ABI means Anheuser-Busch InBev SA/NV, its domestic and foreign parents, predecessors, divisions, subsidiaries, affiliates, partnerships and joint ventures (excluding Crown, and, prior to the completion of the Transaction, Modelo); and all directors, officers, employees, agents, and representatives of the foregoing. The terms “parent,” “subsidiary,” “affiliate,” and “joint venture” refer to any person in which there is majority (greater than 50 percent) or total ownership or control between the company and any other person.

  • API means the American Petroleum Institute.

  • BLS means Basic Life Support.

  • SMI means the a supplier managed inventory service (consignment or imprest stock option) as described further in Call Off Schedule 9;

  • PTC means the tax credit for electricity produced from certain renewable generation resources described in Section 45 of the Internal Revenue Code of 1986, as it may be amended or supplemented from time to time.

  • Licensee has the meaning set forth in the preamble.

  • Bioassay means the determination of kinds, quantities or concentrations and, in some cases, the locations of radioactive material in the human body, whether by direct measurement, in vivo counting, or by analysis and evaluation of materials excreted or removed from the human body. For purposes of these rules, “radiobioassay” is an equivalent term.

  • PPI has the meaning specified in Section 4.2(a);

  • BSC means the balancing and settlement code required to be in place, pursuant to the transmission licence granted to the transmission company in England and Wales, as from time to time modified.

  • Sublicensee means a third party to whom LICENSEE grants a sublicense of certain rights granted to LICENSEE under this Agreement.

  • Regulatory Materials means, with respect to a Licensed Product for any particular indication in any particular jurisdiction, regulatory applications and submissions (and any supplements or amendments thereto), and any notifications, communications, correspondence, registrations, drug master files, Regulatory Approvals and/or other filings made to, received from or otherwise conducted with a Regulatory Authority, including BLAs and INDs, as applicable, that relate to such Licensed Product in such jurisdiction. Regulatory Materials also include presentations, responses, and applications for Regulatory Approvals.