Agreement to Supply Product - Finished Product Sample Clauses

Agreement to Supply Product - Finished Product. 5.2.1 Engagement of Contract Finishers. GelTex shall be responsible for identifying and contracting with a Finisher/Packager to tablet, test, package and label Finished Product. GelTex shall consult with Sankyo regarding the terms of any agreement that GelTex enters into with a Finisher/Packager after the Effective Date. Sankyo shall have the right to consent to the terms of such agreement prior to GelTex's execution thereof, which consent shall not be unreasonably withheld. However, in the event that Sankyo does not consent to the terms which GelTex deems acceptable, the prices set forth in Section 5.2.7 shall be void. In such case, GelTex shall charge Sankyo for the actual price charged by the Finisher/Packager. Sankyo shall have the right to assume full, but not partial, responsibility through, but not limited to, assignment of contract(s) with the Finisher/Packager(s) for conversion and packaging of Finished Product, upon reasonable notice. In addition, following the approval of the Product NDA, Sankyo shall have the right to assume full, but not partial responsibility for the packaging and labeling of the tablets, upon reasonable notice. Notwithstanding the above, Sankyo's right to assume responsibility for production of Finished Product and/or packaging and labeling of tablets shall at all times be subject to Sankyo's agreement to assume the contractual obligations regarding the Manufacture of [ * ] Confidential information omitted and filed separately with the Commission 13 CONFIDENTIAL Finished Product that GelTex has entered into prior to Sankyo's exercise of this right.
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Related to Agreement to Supply Product - Finished Product

  • 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.

  • 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.

  • Product The term “

  • Product Supply 5.2.1 HEMISPHERX undertakes and agrees to supply to IMPATIENTS on an exclusive basis, IMPATIENTS’ requirements of Product ordered in accordance with the terms of this Agreement, for distribution and sale in the Territory, limited to EAP use of Product in accordance with Early Access Approvals.

  • 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.

  • Manufacture of Product Prior to commercialization of the Product, the Parties may, if appropriate for both parties, negotiate in good faith a manufacturing and supply agreement to provide for Licensor to fulfill the manufacturing requirements of Licensee for Product for sale in the European market. The cost of such manufacturing shall not be greater than * percent (*%) of the cost of any competitor cGMP contract manufacturing facility that proposes to manufacturer the Product for Licensee. * Confidential information has been omitted and filed confidentially with the Securities and Exchange Commission.

  • Supply of Product The JDC shall be responsible for determining the sources of, and arrangements for, the manufacture and supply of Products that the JDC believes will result in long-term profit maximization for such Products. The JDC shall endeavor to [ * ].

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

  • Supply Agreement Buyer shall have executed and delivered the Supply Agreement to the Company.

  • Marking of Licensed Products To the extent commercially feasible and consistent with prevailing business practices, Company shall xxxx, and shall cause its Affiliates and Sublicensees to xxxx, all Licensed Products that are manufactured or sold under this Agreement with the number of each issued patent under the Patent Rights that applies to such Licensed Product.

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