Manufacturing and Testing Sample Clauses

Manufacturing and Testing. 5.1. COMPANY is responsible for authorizing the SUPPLIER to MANUFACTURE PRODUCT by issuing a written request such as a CUSTOMER ORDER. X
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Manufacturing and Testing. LTS shall submit to NuPathe all Manufacturing and testing documents relating to any Batch of Drug Product ordered hereunder, including analyses with instrument conditions, within [**] business days of the completion of the Manufacturing process and associated testing with respect to any particular Batch of Drug Product; provided, however, that testing documentation related to microbiologic analyses shall be submitted within [**] days after completion. In addition, LTS shall keep on file all books and records in connection with the Manufacture and testing of the Drug Product, including, but not limited to, those books and records relating to cross-over cleaning, process validation, installation qualification, operational qualification and cleaning validation for a minimum period of three (3) years past the expiration date of the manufactured batch or, in the case of general records, such as equipment qualification and the like, for a minimum period of three (3) years past the expiration date of the last batch manufactured on said equipment.
Sample 1
Manufacturing and Testing documentation, NOVARTIS will assure that these conversions are accurate and updated as appropriate. In addition, where possible, there should be a cross-reference in the master document to the appropriate IDENIX Specification(s).
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Manufacturing and Testing cytostatics or biological preparations from live micro-organisms. NOVARTIS agrees to advise IDENIX by means of a BSE/TSE certificate of compliance mentioning the origin of all bovine, caprine and ovine derived starting materials, if any, purchased by NOVARTIS for the processing of the LdT Finished Products. If a CoA on starting material is provided to IDENIX it shall clearly state the origin of the material.
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Manufacturing and Testing 
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Related to Manufacturing and Testing

  • Manufacturing and Supply Genentech shall be responsible for manufacturing and supplying Licensed Products for clinical use and commercial sale in the Genentech Field.

  • 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 (a) The Supplier shall without limitation be responsible, at no additional cost to the Purchaser, for: sourcing and procuring all raw materials for the Products; obtaining all necessary approvals, permits and licenses for the manufacturing of the Products; providing sufficient qualified staff and workers to perform the obligations under this Purchase Agreement; implementing and maintaining effective inventory and production control procedures with respect to the Products; and handling other matters as reasonably requested by the Purchaser from time to time.

  • Drug Testing (A) The state and the PBA agree to drug testing of employees in accordance with section 112.0455, F.S., the Drug-Free Workplace Act.

  • Product Testing Upon request, Customer shall provide Operator a laboratory report for each Product delivery by Customer or Customer’s supplier. Operator will not be obligated to receive Contaminated Product for throughput through the Pipelines, nor will Operator be obligated to accept Product that fails to meet the applicable quality specifications for the Berths under the BAUTA and any Terminal Service Orders issued thereunder.

  • Packaging and Labeling Seller shall properly xxxx, xxxx, and ship Goods and provide Buyer with shipment documentation showing the Order number, Seller’s identification number for the subject Goods, the quantity of goods in shipment and the number of cartons or containers in the shipment.

  • Random Drug Testing All employees covered by this Agreement shall be subject to random drug testing in accordance with Appendix D.

  • GMP The parties agree that the GMP for the Project is $ , consisting of the Preconstruction Fee, the Estimated Cost of the Work and the CM/GC Fee (stated as a fixed dollar lump sum amount), as follows: Preconstruction Fee: $ Estimated Cost of Work (Est. COW): $ CM/GC Fee ( % of Est. COW): $ GMP (Total of above categories): $ For purposes of determining the GMP, the Estimated Cost of the Work includes the CM/GC’s Contingency, costs for General Conditions Work, and the costs of all components and systems required for a complete, fully functional facility.

  • Manufacturing Services Jabil will manufacture the Product in accordance with the Specifications and any applicable Build Schedules. Jabil will reply to each proposed Build Schedule that is submitted in accordance with the terms of this Agreement by notifying Company of its acceptance or rejection within three (3) business days of receipt of any proposed Build Schedule. In the event of Jabil’s rejection of a proposed Build Schedule, Jabil’s notice of rejection will specify the basis for such rejection. When requested by Company, and subject to appropriate fee and cost adjustments, Jabil will provide Additional Services for existing or future Product manufactured by Jabil. Company shall be solely responsible for the sufficiency and adequacy of the Specifications [***].

  • Laboratory Testing All laboratories selected by UPS Freight for analyzing Controlled Substances Testing will be HHS certified.

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