GRANT OF MANUFACTURING RIGHTS Sample Clauses

GRANT OF MANUFACTURING RIGHTS. (a) The grant of rights in this section only applies to the manufacture, use, and sale of Product for which the Customer has submitted a purchase order that has been accepted by Paramit. Portions of this Exhibit, indicated by the xxxx “[***],” were omitted and have been filed separately with the Securities and Exchange Commission pursuant to the Registrant’s application requesting confidential treatment pursuant to Rule 406 of the Securities Act of 1933, as amended.
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GRANT OF MANUFACTURING RIGHTS. Selamine and its Affiliates hereby grant to King and its Affiliates, during the Term, an exclusive (except as to Selamine) license or sublicense, as the case may be, with the right to sublicense under the Ramipril Patents to make [***], provided that such [***] may be sold only in the Territory, and provided further that such license shall be subject to the terms and conditions of this Agreement and shall be exercisable only (a) on the occurrence of any of the events identified in Section 4.2 of the Product Supply Agreement or (b) in the event the Product Supply Agreement is terminated by King for Selamine's or its Affiliate's material breach.
GRANT OF MANUFACTURING RIGHTS. (a) Integrated agrees that the PRODUCT will be manufactured in accordance with (i) all laws and regulations of Ontario; and (ii) the local laws and regulations of the countries and jurisdictions where the PRODUCT will be distributed and sold, provided that PPK shall first provide written notification to Integrated of variations or changes in local laws and regulations which are to be adhered to, where they differ from Ontario laws and regulations.
GRANT OF MANUFACTURING RIGHTS. (a) The grant of rights in this section only applies to the manufacture, use, and sale of product for which:
GRANT OF MANUFACTURING RIGHTS. In the event that FNS demonstrates that FNS can manufacture SDS Inc. Products of equal quality as those of SDS Singapore as determined by SDS Inc. (or any one of the Products) in India at a cost equal to or less than the price (including freight) ,charged by SDS Singapore to FNS for such Products (or one of the Products, as the case may be), then, in consideration of FNS' promise to pay a certain royalty as set forth in paragraph 6f hereinafter, SDS Singapore shall grant to FNS a complete assignment and transfer of its rights to manufacture in India under the License Agreement (hereinafter referred to as the "Manufacturing Rights") the Products for distribution and sale within India for the term of this Agreement and any extensions 4 5 hereof, SDS Inc., recognizing that a grant hereunder of Manufacturing Rights will further the purposes of SDS Inc. under the License Agreement, hereby consents to such grant of the Manufacturing Rights, SDS Inc. shall have the right to establish, maintain and monitor quality control manufacturing standards (equal to those applicable to SDS Singapore) which FNS shall adhere to in its manufacturing operations. SDS Singapore shall have the right to purchase Products manufactured by FNS in India for distribution and sale by SDS Singapore in the territory, excluding India, covered by the License Agreement, provided that FNS may allocate a portion or all of its manufacturing capacity and production to satisfy its own distribution and sale needs within India.
GRANT OF MANUFACTURING RIGHTS. Notwithstanding the foregoing provisions, DCI hereby grants to CRTX the right to manufacture the Products in quantities sufficient to meet the forecast demand in the CF Market, but that right shall be exercisable only in the event that (A) DCI fails to meet forecast demand for six (6) consecutive months, or (B) there is a Force Majeure event (as defined in Section 19) that prevents DCI from supplying the Products. [***] Confidential portions of the exhibit have been omitted and filed separately with the Securities and Exchange Commission. Corrected and Restated
GRANT OF MANUFACTURING RIGHTS. Notwithstanding the provisions of Article 6 above, in the event that it is not commercially feasible for Eisai to distribute, sell and market any Product in the Territory at the price charged to Eisai by Paravax for such Product, or that Paravax materially breaches its obligations pursuant to terms of the Supply Agreement to supply Eisai's requirements for Products for distribution and sale in the Territory, Paravax shall grant to Eisai the exclusive rights (with the right to sublicense) to manufacture the Product for distribution, sale and marketing in the Territory to the extent permitted by Article 1 of this Agreement.
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GRANT OF MANUFACTURING RIGHTS. CORNERSTONE hereby grants to VINTAGE the exclusive right to manufacture the Product(s) for sale to CORNERSTONE. VINTAGE agrees not to enter into any subcontracts or other agreements for the Product(s) in order to satisfy its obligations under this Agreement without prior written approval from the CORNERSTONE.
GRANT OF MANUFACTURING RIGHTS. Arrow and its Affiliates hereby grants to King and its Affiliates, during the Term, an exclusive (except as to Arrow and its Affiliates) right, with the right to sublicense, under the Ramipril Application, the Amended Ramipril Application and the Ramipril Know-How solely to manufacture [***], provided that such [***] may be sold only in the Territory, and provided further that such license shall be subject to the terms and conditions of this Agreement and shall be exercisable only (a) on the occurrence of any of the events identified in Section 4.2 of the Product Supply Agreement or (b) in the event the Product Supply Agreement is terminated by King for Arrow's material breach. At King's reasonable request, Arrow and its Affiliates shall cooperate with King in effecting a Tech Transfer to King and King's Affiliates with respect to [***]. Each Party shall bear its own costs in connection with any Tech Transfer.

Related to GRANT OF MANUFACTURING RIGHTS

  • Manufacturing Rights Manufacturing Rights will be governed by Attachment 6.

  • Supply of Materials The following materials will be supplied by the department Name of Materials Rate. Place of delivery 1.

  • Manufacturing Technology Transfer With respect to each Technology Transfer Product, upon AbbVie’s written request after the Inclusion Date for the Included Target to which such Technology Transfer Product is Directed, Morphic shall effect a full transfer to AbbVie or its designee (which designee may be an Affiliate or a Third Party manufacturer) of all Morphic Know-How and Joint Know-How relating to the then-current process for the Manufacture of such Technology Transfer Product (the “Manufacturing Process”) and to implement the Manufacturing Process at facilities designated by AbbVie (such transfer and implementation, as more fully described in this Section 5.3, the “Manufacturing Technology Transfer”). To assist with the Manufacturing Technology Transfer, Morphic will make its personnel reasonably available to AbbVie during normal business hours for up to [***] FTE hours with respect to each Included Target (in each case, free of charge to AbbVie) to transfer and implement the Manufacturing Process under this Section 5.3. Thereafter, if requested by AbbVie, Morphic shall continue to perform such obligations; provided, that AbbVie will reimburse Morphic for its full-time equivalent (FTE) costs (for clarity, in excess of [***] FTE hours) and any reasonable and verifiable out-of-pocket costs incurred in providing such assistance. CERTAIN CONFIDENTIAL INFORMATION CONTAINED IN THIS DOCUMENT, MARKED BY [***], HAS BEEN OMITTED BECAUSE IT IS NOT MATERIAL AND WOULD LIKELY CAUSE COMPETITIVE HARM TO THE COMPANY IF PUBLICLY DISCLOSED.

  • Development of Products (a) During the term of this Agreement, ViewRay may from time to time seek services from PEKO with respect to the development of certain Products that can be incorporated into the ViewRay Renaissance™ MRI-guided radiation therapy system. For each Program to be undertaken by PEKO pursuant to this Agreement, the parties will prepare a “Work Statement” and agree to said “Work Statement” in substantially the form attached as Attachment 1. Each Work Statement will describe: (i) the (i) services that PEKO will be responsible for providing to ViewRay and the deliverables that PEKO will be responsible for delivering to ViewRay (“Deliverable(s)”), (ii) delivery schedule for the Deliverables, (iii) pricing terms, (iv) work plan for the Program, and (v) ViewRay’s responsibilities in connection with the Program. Each Work Statement will be prepared based upon the requirements and information provided to PEKO by ViewRay. A separate Work Statement will be required for each Program; and each Work Statement will become subject to this Agreement only when mutually agreed and signed by ViewRay and PEKO.

  • Manufacture 2.1. The LED(s) on the LED module shall be equipped with suitable fixation elements.

  • Transfer of Materials In the event Acceleron exercises its rights pursuant to Section 10.5.1, Celgene shall negotiate in good faith with Acceleron regarding Celgene transferring to Acceleron, at Acceleron’s cost, materials developed under this Agreement in the course of Developing and Commercializing Licensed Compounds or Licensed Products that are directly related to Licensed Compounds or Licensed Products to the extent provided in and in accordance with such agreement.

  • Sublicensing Rights Novartis and its Affiliates may grant sublicenses of the license granted in Section 5.3.1(a), Section 5.3.2, and Section 5.3.3, and Intellia and its Affiliates may grant sublicenses of the license granted in Section 5.3.1(b), provided that (a) such sublicense (i) is in writing, (ii) is subject and subordinate to, and consistent with, the terms and conditions of this Agreement, and (iii) requires the applicable sublicensee to comply with all applicable terms of this Agreement [***]; (b) with respect to Novartis or any of its Affiliates as the sublicensing Party to the extent required by the Key License Agreements as in effect on the Effective Date or the agreements for any Included Intellia New In-Licensed Intellectual Property, Novartis promptly notifies Intellia of the grant of each sublicense and provides Intellia a copy of the final executed sublicense agreement, redacted for information not pertinent to this Agreement to the extent that such redactions do not reasonably impair Intellia’s ability to ensure compliance with this Agreement, the Key License Agreements or agreements for any Included Intellia New In-Licensed Intellectual Property, as applicable, (c) Novartis or Intellia, as applicable, shall be responsible for the failure by its sublicensees to comply with, and Novartis or Intellia, as applicable, guarantees the compliance by each of its sublicensees with, all relevant restrictions, limitations and obligations in this Agreement, and [***]. CERTAIN CONFIDENTIAL PORTIONS OF THIS EXHIBIT WERE OMITTED AND REPLACED WITH “[***]”. A COMPLETE VERSION OF THIS EXHIBIT HAS BEEN FILED SEPARATELY WITH THE SECRETARY OF THE SECURITIES AND EXCHANGE COMMISSION PURSUANT TO AN APPLICATION REQUESTING CONFIDENTIAL TREATMENT PURSUANT TO RULE 406 PROMULGATED UNDER THE SECURITIES ACT OF 1933, AS AMENDED.

  • Manufacturing Agreement Each of the Sellers (as applicable) shall have executed and delivered to the Buyer the Manufacturing Agreement with respect to the portion of the Business conducted at the applicable Facility.

  • Commercialization License Subject to the terms of this Agreement, including without limitation Section 2.2 and Theravance's Co-Promotion rights in Section 5.3.2, Theravance hereby grants to GSK, and GSK accepts, an exclusive license under the Theravance Patents and Theravance Know-How to make, have made, use, sell, offer for sale and import Alliance Products in the Territory.

  • Licensed Products Lessee will obtain no title to Licensed Products which will at all times remain the property of the owner of the Licensed Products. A license from the owner may be required and it is Lessee's responsibility to obtain any required license before the use of the Licensed Products. Lessee agrees to treat the Licensed Products as confidential information of the owner, to observe all copyright restrictions, and not to reproduce or sell the Licensed Products.

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