Co-Marketing Rights Sample Clauses

Co-Marketing Rights. Argent shall have the right of first refusal to employ its own sales representatives to co-market and sell the Products in those areas of the Territories in which TEAMM does not have a sales representative. A separate agreement will be developed at such time as TEAMM and Argent should choose to explore this option.
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Co-Marketing Rights. If Nycomed should fail (through no fault of Acusphere and without Good Reason) to achieve, in any Primary Jurisdiction or in the Secondary Jurisdictions taken as a whole, the Minimum Sales Target in such Primary Jurisdiction or the aggregate Minimum Sales Target for the Secondary Jurisdictions as set forth in the Sales Forecast then, and only if either of such events occur [CONFIDENTIAL TREATMENT REQUESTED] /*/, Acusphere shall have the right and option, exercisable in its sole discretion, by written notice to that effect delivered by Acusphere to Nycomed within sixty (60) days after said events occur, to co-market the Product in such Primary Jurisdiction or in each particular Secondary Jurisdiction in which Nycomed has failed to meet its Minimum Sales Target, either by itself or in conjunction with another entity. If Acusphere exercises its right to co-market the Product in such Jurisdiction the following shall occur, to the extent allowed by Applicable Laws: (i) the license granted to Nycomed by Acusphere under Section 3.02 shall thereafter be deemed to be a non-exclusive license within such Jurisdiction ([CONFIDENTIAL TREATMENT REQUESTED] /*/); (ii) Nycomed shall grant and hereby does grant to Acusphere an irrevocable, non-exclusive, royalty-free license, with the right to sublicense, to use the Clinical Documentation, the Results and the Marketing Authorizations and make any filings required by Nycomed with the Competent Authorities, to the extent legally permissible, in connection with such activities and only for the Jurisdiction in question; (iii) Nycomed shall cooperate with Acusphere in obtaining the necessary Marketing Authorizations in a timely manner, at Acusphere's expense; (iv) Acusphere will be solely 44
Co-Marketing Rights. (a) Subject to the earlier exercise of co-marketing rights which may occur pursuant to subpart (c) below, the parties agree that Pharmos shall be entitled upon written notice to BLP to co- market, distribute and sell each Drug Product under labeling belonging to Pharmos in the Territory commencing on the second (2nd) anniversary of the earlier to occur of (i) the first Commercial Sale of such Drug Product by BLP, or (ii) the later of (X) April 1, 1996, or (Y) the ninetieth day following FDA approval of the NDA for such Drug Product (unless BLP has been restrained from making commercial sales of such Drug Product through no fault of BLP within such ninety (90) day period, in which case such ninety (90) day period shall be deemed to have commenced on the first day on which such restraint no longer exists). (b) Upon the written request of BLP, Pharmos agrees that it will delay exercise of the rights reserved to Pharmos in subsection (a) above with respect to any Drug Product for a period of up to 365 days if (i) LET has not entered Phase III clinical studies on or before the second anniversary of this Agreement based on an R&D Plan (defined below) previously approved by the parties, or (ii) LEA has not entered Phase III clinical studies on or before the second anniversary of this Agreement based on an R&D Plan previously approved by the parties, or (iii) Phase II clinical studies for either LET or LEA have not substantially complied with the protocols, or satisfied safety and efficacy targets, defined in the relevant R&D Plan for each such substance, provided that no delay shall occur pursuant to this subsection (b) if the events described in subparts (i), (ii) or (iii) shall failed to have occurred solely as a result of the failure of BLP to provide Pharmos with appropriate clinical trial materials of LEA or LET, as the case may be, in conformity with their respective Specifications (other than such failure resulting from the failure of Pharmos to deliver appropriate Drug Substance for the production of such clinical Trial materials). (c) In addition to the co-marketing rights described above, from and after the last Payment Date for a Product Year in which BLP fails to pay the Exclusivity Amount for a particular Drug Product, Pharmos shall be entitled to (i) co-market such Drug Product in the Territory, and (ii) subject to delivery of a written notice delivered to BLP no later than sixty (60) days following the last day of the Product Year in question, at a...
Co-Marketing Rights. 13.1 In the event the parties enter into one or more licenses as provided in Section 12.2 above, [**see cover page note] shall retain the right, but not the responsibility or obligation, for DMI and COGENCO to assist such licensees in marketing the Product(s) for the Field within the Territory or part of the Territory that is licensed ("Co-Marketing Rights"), based on the principle of maximizing profits from sales of Product(s). These Co-Marketing Rights shall include the right to make, have made, use, sell, offer for sale, commercialize, import and export Product(s) to the extent necessary for DMI and COGENCO to be able to market and/or Promote Product(s) for the Field within the Territory or part of the Territory that is licensed. DMI and Cogenco shall coordinate their respective marketing efforts in light of the overall market strategy determined by the licensee(s) within the Territory. 13.2 DMI hereby grants to COGENCO a license of all of its Intellectual Property covering or relating to the treatment of multiple sclerosis with DMI-13-9523 to the extent needed by COGENCO to fully exercise the Co-Marketing Rights it receives pursuant to the terms of Section 13.1. 13.3 DMI shall have the right to license its Co-Marketing Rights to Third Parties with the approval of the licensee(s) within the Territory. 13.4 COGENCO shall have the right to sublicense its Co-Marketing Rights to Third Parties with the approval of the licensee(s) within the Territory.
Co-Marketing Rights. 13.1 In the event the parties enter into one or more licenses as provided in Section 12.2 above, [**see cover page note] shall retain the right, but not the responsibility or obligation, for DMI and COGENCO - to market and/or promote Product(s) for the Field within the Territory or part of the Territory - that is licensed ("Co-Marketing Rights"). These Co-Marketing Rights shall include the right to make, have made, use, sell, offer for sale, commercialize, import and export Product(s) to the extent necessary for DMI and COGENCO to be able to market and/or promote Product(s) for the Field within the Territory or part of the Territory that is licensed. 13.2 DMI hereby grants to COGENCO a license of all of its Intellectual Property covering or relating to the treatment of asthma in humans with a [**see cover page note] to the extent needed by COGENCO to fully exercise the Co-Marketing Rights it receives pursuant to the terms of Section 13.1. 13.3 DMI shall have the right to license its Co-Marketing Rights to Third Parties with the approval of COGENCO. 13.4 COGENCO shall have the right to sublicense its Co-Marketing Rights to Third Parties with the approval of DMI.
Co-Marketing Rights. If the Company gives BSC written notice [ ** ] then the Company will have co-exclusive rights, with BSC and BSC's subdistributors, to market and distribute the Products in such country for the balance of the term of this Agreement unless [ ** ].

Related to Co-Marketing Rights

  • Marketing Rights Neither the Company nor any of its Subsidiaries have granted rights to license, market, or sell its products or services to any other Person and is not bound by any agreement that affects the Company’s (or any Subsidiary’s) exclusive right to develop, distribute, market or sell its products or services.

  • Manufacturing and Marketing Rights The Company has not granted rights to manufacture, produce, assemble, license, market, or sell its products to any other person and is not bound by any agreement that affects the Company's exclusive right to develop, manufacture, assemble, distribute, market, or sell its products.

  • Manufacturing Rights (a) If QED fails to supply Product ordered by ViewRay in accordance with the terms of this Agreement regarding the quantity or quality of Products supplied to ViewRay, then QED shall within fifteen (15) Business Days of said failure present ViewRay with a plan to remedy the problem and shall use Commercially Reasonable Efforts to execute such plan and remedy the problem or QED shall secure an alternative source of supply within a reasonable time at no additional cost to ViewRay. Any such alternative source of supply shall be on terms substantially identical with the terms of this Agreement. If QED is unable to provide a plan to remedy the problem or secure an alternative source of supply within [***] after its initial failure to supply, then QED shall consult with ViewRay and the parties shall work together to remedy the problem. If QED is unable to remedy the supply problem after [***] (or longer as agreed in writing by the parties), commencing with the date upon which such failure to supply began, then ViewRay may at its option, and upon notice to QED, manufacture the Products itself or through a third party in accordance with the provisions of Section 3.10(b). [***] Certain information in this document has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions. (b) If ViewRay notifies QED pursuant to Section 3.10(a), above, that ViewRay will manufacture the Products itself or through a third party, QED shall (i) deliver to ViewRay within thirty (30) days media embodying or disclosing all Program technology and Program proprietary or intellectual property rights necessary to enable ViewRay or its designee to manufacture Products conforming with the Specifications; and (ii) provide ViewRay or its designee, upon request, with reasonable assistance in establishing a back-up manufacturing line. ViewRay shall require any third party ViewRay designates to manufacture Products pursuant to this Section 3.10, to agree in writing to observe the terms of this Agreement relating to confidentiality and the manufacture of Products. Notwithstanding any provision of this Section 3.10 to the contrary, in no case shall QED be required to pay ViewRay in respect of any Products purchased by ViewRay from a third party operating a back-up manufacturing line established pursuant to this Section 3.10 or manufactured by ViewRay or its Affiliates pursuant to this Section 3.10.

  • Sublicensing Rights (a) The license(s) granted to Intellia in Section 2.1 and to Caribou in Section 2.2 may be sublicensed, in full or in part, by Intellia and Caribou, respectively, (each, the “Sublicensing Party”) by a written agreement to its Affiliates and Third Parties (with the further right to sublicense [***] provided that the following shall likewise apply with respect to sublicenses granted by a Sublicensee), provided, that: (i) the Sublicensing Party will provide to the other Party a copy of any sublicense agreement with a Sublicensee within [***] days of execution thereof, which sublicense agreement may be redacted as necessary to protect commercially sensitive information to the extent such information is not reasonably necessary to determine compliance with this Agreement or to determine the rights granted under any of the Caribou IP or Intellia IP, as applicable (together with an accurate English translation of such sublicense, if applicable) provided that if such agreement is with a Related Party the Sublicensing Party shall provide an unredacted copy thereof; (ii) the Sublicensing Party will be responsible for any and all obligations of such Sublicensee as if such Sublicensee were “Intellia” or “Caribou”, as applicable, hereunder; (iii) any such Sublicensee will agree in writing to be bound by identical obligations as the Sublicensing Party hereunder with respect to the activities of such Sublicensee hereunder; (iv) to the extent that the Sublicensing Party or any Sublicensee grants a sublicense under any intellectual property subject to a Caribou In-License or Intellia Included In-License, as applicable, such sublicense (and such further sublicensee) will be subject to the terms of such Caribou In-License or Intellia Included In-License, including such sublicensee’s compliance with the Required In-License Provisions [***].

  • Billing Rights Information on your rights to dispute transactions and how to exercise those rights is provided in your account agreement.

  • Third-Party Offerings Dell may offer Third-Party Products for use with the APEX Service through an online marketplace, or using Dell’s then-current Third-Party Product resale programs (e.g. “Extended Technologies Complete”, “Software & Peripherals (S&P)”). Third-Party Products that Distributor orders from Dell through these resale programs are referred to as “Third-Party Offerings”. Distributor may offer Third-Party Offerings to Reseller to offer to Customer for Customer’s use, at Distributor’s option, if available. If Distributor chooses to offer Third-Party Offerings to Reseller for Reseller to offer to Customer for Customer’s use, Distributor, Reseller, and Customer are responsible for complying with any terms applicable to the Third-Party Offerings, including any separate fees imposed by the provider of that Third-Party Offering (whether payable to Dell or directly to the third-party provider). Distributor agrees to comply with the standard license, services, warranty, indemnity, and support terms of the third-party manufacturer/supplier (or an applicable direct agreement between Distributor and the third-party manufacturer/supplier) for the Third Party Offering. Even if Dell invoices for them, Dell does not provide support services for Third-Party Offerings. Distributor must contact the applicable third-party directly for support. Third-Party Offerings are provided “AS IS”. Any warranty, damages or indemnity claims against Dell for Third-Party Offerings are expressly excluded. Dell may suspend or terminate provision and hosting of any Third- Party Offerings at any time, and that suspension or termination will not be deemed a material change to the APEX Service for the purpose of Clause 3.2 (Material Modifications).

  • Non-Marketing Purposes Enertech Information Systems, Inc. greatly respects your privacy. We do maintain and reserve the right to contact you if needed for non-marketing purposes (such as bug alerts, security breaches, account issues, and/or changes in Enertech Information Systems, Inc. products and services). In certain circumstances, we may use our website, newspapers, or other public means to post a notice. Enertech Information Systems, Inc.'s website is not directed to, and does not knowingly collect personal identifiable information from, children under the age of thirteen (13). If it is determined that such information has been inadvertently collected on anyone under the age of thirteen (13), we shall immediately take the necessary steps to ensure that such information is deleted from our system's database, or in the alternative, that verifiable parental consent is obtained for the use and storage of such information. Anyone under the age of thirteen (13) must seek and obtain parent or guardian permission to use this website.

  • Joint Marketing ‌ The parties will consult about undertaking joint marketing of the Customer’s Services and the Network.

  • Competing Products The provisions of Section 21 are set forth on attached Exhibit H and are incorporated in this Section 21 by this reference.

  • Commercialization Intrexon shall have the right to develop and Commercialize the Reverted Products itself or with one or more Third Parties, and shall have the right, without obligation to Fibrocell, to take any such actions in connection with such activities as Intrexon (or its designee), at its discretion, deems appropriate.

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