POWDERJECT NAMED PRODUCTS Sample Clauses

POWDERJECT NAMED PRODUCTS. PRL may request designation of a particular Selectable Product (which is not at that time an AlgoRx Named Product) as a "POWDERJECT NAMED PRODUCT" by submitting a written request to AlgoRx, identifying the specific moiety and the specific intended application, provided that PRL or its Affiliate (a) has commenced research of such product for use in the PowderJect Group's Field, or (b) has a firm plan (including an established budget) for commencing a research and development program to develop such product within six (6) months, or (c) is engaged in active negotiations with a Third Party regarding granting such Third Party a license to such product for use in the PowderJect Group's Field. Unless AlgoRx has already designated such product as an AlgoRx Named Product in accordance with Section 2.3(a), such product shall be automatically designated a PowderJect Named Product on the date that is thirty (30) days after the date of such request, and, subject to the diligence obligations under Section 2.3(c), shall not be available for development and commercialization by AlgoRx in the Licensed Field and PRL shall thereafter have exclusive rights to develop and commercialize such product in the Powderject Group's Field under the license granted to it in Section 2.2. Further, if a particular Selectable Product, that PRL wishes to designate as a PowderJect Named Product as provided above, is a member of a closely-related class of compounds with similar biological or pharmacological activity, PRL may, at the time PRL makes the written request as above, also submit a request for designation of such whole class of Selectable Products as PowderJect Named Products (but excluding any such Selectable Products that were previously designated as AlgoRx Named Products in accordance with Section 2.3(a)), which request shall specify the particular Selectable Products that are part of such class and subject to such request and the reasons supporting such designation. In such case, AlgoRx may not submit any request under Section 2.3(a) covering any of the Selectable Products that are subject of such request, for a period of 120 days thereafter. Promptly after any such request, the Parties shall meet and shall discuss reasonably and in good faith to arrive at an agreement on the scope of the class of such Selectable Products that shall be deemed to be PowderJect Named Products, with the intention that such group of PowderJect Named Products shall be limited to the class that truly ...
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Related to POWDERJECT NAMED PRODUCTS

  • Product The term “

  • API A. Reliant shall supply to Cardinal Health for Manufacturing and Packaging, at Reliant’s sole cost, the API and applicable reference standards in quantities sufficient to meet Reliant’s requirements for each Product as further set forth in Article 4. Prior to delivery of any of the API or reference standard to Cardinal Health for Manufacturing and Packaging, Reliant shall provide to Cardinal Health a copy of the API Material Safety Data Sheet (“MSDS”), as amended, and any subsequent revisions thereto. Reliant shall supply the API, reference standards, and Certificate of Analysis FOB the Facility no later than thirty (30) days before the scheduled Manufacture Date upon which such API will be used by Cardinal Health. Upon receipt of the API, Cardinal Health shall conduct identification testing of the API. Cardinal Health shall use the API solely and exclusively for Manufacturing and Packaging under this Agreement. The maximum volume of API that Reliant supplies to Cardinal Health shall not exceed the amount reflected in the Firm Commitment and the next six (6) months of the Rolling Forecast.

  • 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.

  • New Products You agree to comply with NASD Notice to Members 5-26 recommending best practices for reviewing new products.

  • Manufacture (a) Manufacturer shall only manufacture the specific number of Products as requested by Company and at no time shall manufacture excess goods or overruns. Manufacturer shall not sell any Products bearing the Trademarks to any third parties without the express written consent of Company.

  • Products 1.1. The information (including but not limited to the quantity, rated hashrate, unit price (“Unit Price”), total price for one item (“Total Price (One Item)”), total price for all the items (“Total Purchase Price”) of Products to be purchased by Party B from Party A is as follows (“Products”):

  • Manufacturing License Subject to the terms of this Agreement, including without limitation Section 2.2, Theravance grants to GSK an exclusive license under the Theravance Patents and Theravance Know-How to make and have made API Compound or formulated Alliance Product in the Territory.

  • Licensed Product “Licensed Product” shall mean any article, composition, apparatus, substance, chemical material, method, process or service whose manufacture, use, or sale is covered or claimed by a Valid Claim within the Patent Rights. For clarity, a “Licensed Product” shall not include other product or material that (a) is used in combination with Licensed Product, and (b) does not constitute an article, composition, apparatus, substance, chemical material, method, process or service whose manufacture, use, or sale is covered or claimed by a Valid Claim within the Patent Rights.

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

  • Additional Products Throughout the Term, Rockwell shall provide to DaVita and the DaVita Facilities the right to purchase and/or lease all current or new products manufactured, utilized, licensed, sold or distributed by Rockwell or any of its Affiliates (including products and product lines acquired by Rockwell or any of its Affiliates as a result of an acquisition, merger or other transaction involving Rockwell or any of its Affiliates) that are or that become Commercially Available and which are not already covered by this Agreement or by any other agreement, whether written or oral, between the parties hereto (such products are collectively referred to as “Additional Products” and individually as an “Additional Product”). Rockwell agrees to include DaVita in all of its and its Affiliates distributions of customer announcements regarding Rockwell’s or its Affiliates’ Additional Products. The purchase price for any such Additional Products shall be negotiated by the parties hereto in good faith and the agreed upon purchase price shall be memorialized in writing as a supplement or amendment to this Agreement. Rockwell covenants and agrees that it shall only make an offer for the sale of any Additional Product(s) to DaVita’s Vice-President of Clinical Operations, Chief Medical Officer, or Vice-President of Purchasing, and not to any DaVita Facility directly; provided that the purchase of any Additional Product by DaVita or any DaVita Facility through a Rockwell product catalog made generally available to the dialysis community shall not be a breach by Rockwell of this Section 8.1. If Rockwell or any of its Affiliates acquires any Additional Product(s) as a result of an acquisition, merger or other transaction involving Rockwell or any of its Affiliates with a Person with which DaVita or a DaVita Facility, as applicable, already has a purchase or rebate arrangement whether written or oral (a “Prior Agreement”), Rockwell or such Affiliate covenants and agrees that it shall continue to abide by all of the terms and conditions of such Prior Agreement or if DaVita requests, such Additional Product(s) shall be included in this Agreement on terms to be negotiated and determined by the parties hereto as provided in this Section 8.1.

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