Quality Testing. 2.5.1. Magellan reserves the right to perform quality control testing. Any quality testing performed will be made in accordance with American Society for Testing and Materials (ASTM) standards or other industry accepted testing methods as found in industry standards, recommended practices, guides and manuals. The results of tests made by Magellan will be conclusive and binding on both Parties, except in the event of fraud or manifest error.
2.5.2. Customer may test the quality of the Product, at Customer’s sole expense, prior to such Product being delivered to a Vessel and Customer will provide a copy of such test results to Magellan within one business day after the date the sample was taken. If Customer fails to test the quality of any Product prior to loading onto a Vessel or fails to provide notice of any claim on or before the 5th day after the Product has been loaded onto a Vessel, any claim against Magellan for degradation or contamination of that Product will be deemed waived.
Quality Testing. Techniclone shall perform quality control tests and assays on Antibody and Product, including Packaged Product, manufactured and/or packaged by it and its Third Party manufacturers and suppliers pursuant to Section 7.01 in accordance with the requirements of the applicable Drug Approval Application. Techniclone shall provide Schering with a copy of the batch record, a certificate of analysis and a certificate of compliance for each batch of Antibody and Product, including Packaged Product, manufactured by or on behalf of Techniclone, promptly following final quality control release. The certificate of compliance shall certify that each batch was reviewed and meets all regulatory requirements. The certificate of analysis shall certify that each batch was tested and meets all specifications.
Quality Testing. CIL shall have the right to test PRODUCTS and RAW MATERIALS for the conformance with the specifications upon receipt of such PRODUCTS, and agrees to notify ENZO of acceptance or non-acceptance based on such conformity with the specifications within thirty (30) days in the case of RAW MATERIALS and ten (10) days in case of all other PRODUCTS. Acceptance shall not be unreasonably withheld.
Quality Testing. CTI shall perform quality control --------------- tests and assays on all Collaboration Compounds in accordance with the specifications. Furthermore, CTI shall provide ORTHO with a Certificate of Analysis and a Certificate of Compliance for each batch of Collaboration Compound delivered to ORTHO. The Certificate of Compliance shall certify that each batch was reviewed and meets all regulatory requirements. The Certificate of Analysis shall certify that each batch was tested and meets all specifications. CTI shall permit ORTHO's designated representatives to inspect and visit from time to time the facilities at which Collaboration Compounds are manufactured, stored or tested for the purpose of determining compliance with this Agreement, as well as all pertinent regulatory requirements. Such inspections shall occur during regular business hours upon reasonable notice.
Quality Testing. Buyer’s acceptance shall be conditioned upon testing a representative sample from various loads of delivered chips using a chip classifier and a chip sample collection process meeting generally accepted industry standards.
Quality Testing. Alliance shall perform quality control tests and assays on the Product manufactured by it pursuant to Section 9.01 in accordance with the requirements of the applicable Drug Approval Application. Alliance shall provide Schering with a copy of the batch record, a certificate of analysis and a certificate of compliance for each batch of Product delivered to Schering either in advance of or contemporaneous with the delivery of each batch of Product to Schering. The certificate of compliance shall certify that each batch was reviewed and meets all regulatory requirements. The certificate of analysis shall certify that each batch was tested and meets all specifications.
Quality Testing. (a) During the hours of operation referenced in Section 2.08, Sterling shall (i) inspect, sample and test each lot of Raw Materials, Ancillary Raw Materials and Products under the procedures set forth in the Quality Assurance Manual, (ii) code to identify Raw Materials and Ancillary Raw Materials to specific Products produced and shipped and (iii) perform such additional testing, statistical process control and statistical quality control for Products as may be reasonably requested by BASF. BASF shall also have the right to further test Products prior to shipment hereunder. Sterling shall cooperate in any such test, and shall have the right to be represented and to participate in any such test, and to inspect any equipment used in determining the nature or quality of any Product. The cost of all inspecting, sampling, testing and coding hereunder shall be included in Fixed Costs. All records or certifications shall be kept for a period of not less than one year (or for the duration of any contest with respect thereto, if longer), and all samples shall be kept for a period of not less than 90 Days (or for the duration of any contest with respect thereto, if longer), with the procedures for taking samples at the unloading flange for Raw Materials and the procedures for taking samples of Products as of the date of shipment to be mutually agreed upon by the Parties. All records, certifications and samples shall be made available to BASF on request. The retained sample for any Raw Materials or Ancillary Raw Materials shall be the exclusive source for determining whether any Raw Materials or Ancillary Raw Materials meet the applicable Raw Materials Specifications, and the retained sample for any Product shall be the exclusive source for determining whether any Product meets the applicable Product Specifications.
(b) Subject to the terms of this Agreement, Sterling shall accept any and all deliveries of Raw Materials; provided, however, that Sterling may reject any delivery of Raw Materials if Sterling notifies BASF in writing, within 10 Business Days after the delivery of such Raw Materials to Sterling, of the failure of such Raw Materials to meet the applicable Raw Materials Specifications. In the event that Sterling rejects any delivery of Raw Materials, BASF may object to such rejection in writing within five Business Days after receipt of the relevant notice from Sterling, in which event the Parties will meet within three Business Days after delivery of such ...
Quality Testing. Products purchased shall meet the specifications set forth in the applicable Schedule, and the quality determination shall be made by the test methods mutually agreed by the Parties to be industry standards for each Product. Composite samples, continuous samples, or both will be reported by Frontier with respect to each Product at mutually agreed locations. 10.
Quality Testing. Not later than [***] after completion of the manufacturing of the Prototypes, MS shall complete quality testing (the “Quality Testing”) on the Prototypes. Pursuant to Annex 5, a vehicle usage contract must be executed with respect to all Prototypes used by MS in Quality Testing.
Quality Testing. All the Surgical & Suture items supplied by the Supplier shall be subjected to rigorous Analytical Testing or their quality. Samples o each batch o each product supplied will be drawn at the points o supply or distribution / storage and send by the Purchaser to di erent Analytical Laboratories selected by him at his discretion or testing. The samples will be drawn periodically through out the xxxx xx e period. The expenditure towards the Handling and Testing o such samples will be borne by the Supplier at the rates ixed by the Purchaser.
