Quality Testing Clause Samples
The Quality Testing clause establishes the standards and procedures for evaluating whether goods or services meet specified quality requirements before acceptance. Typically, this clause outlines the methods of inspection, the criteria for passing or failing, and the responsibilities of each party in conducting or facilitating tests. For example, it may require the supplier to provide samples for laboratory analysis or allow the buyer to perform on-site inspections. Its core function is to ensure that only products or services that meet agreed-upon quality benchmarks are accepted, thereby reducing the risk of defects and disputes.
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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. 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. 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. 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. (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.
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. CIL shall have the right to test PRODUCTS and * 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 * other PRODUCTS. Acceptance shall not be unreasonably withheld.
Quality Testing. 2.1.1 As promptly as practicable, Microsoft and Yahoo! will work together to define fair, representative and unbiased (a) methodologies and standards for calculating [*] and [*] scores for the primary Microsoft and Yahoo! Algorithmic Search Services (using their primary Web sites, e.g., ▇▇▇▇.▇▇▇ and ▇▇▇▇▇.▇▇▇) in each of the [*] Countries (as defined below) taking into account Yahoo! data sets and (b) similar methodologies and standards for measuring quality for Image Internet Search and Video Internet Search ((a) and (b) collectively, the “Mutual Quality Standards”). Microsoft will also document and share with Yahoo! Microsoft’s own methodology and standards for calculating [*] and [*] scores (which methodologies and standards will be fair, representative and unbiased using Microsoft’s data sets) for the primary Microsoft and Yahoo! Algorithmic Search Services in the [*] Countries (the “[*] Transition Standards”). The “[*] Countries” are the following countries: [*]. As promptly as practicable, Microsoft and Yahoo! will equally fund and begin to measure (or jointly select and pay for a [*] Indicates that certain information in this exhibit has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to omitted portions. third party to measure) against the Mutual Quality Standards and the [*] Transition Standards for the Microsoft and Yahoo! Algorithmic Search Services in the [*] Countries.
2.1.2 In connection with the transition to Microsoft’s Algorithmic Search Services in each [*] Country, Microsoft will notify Yahoo! when it is capable of meeting the SLA and demonstrates that Microsoft’s Algorithmic Search Services’ [*] scores are [*] than Yahoo!’s [*] scores (when such scores are measured on a [*]) in such country using the [*] Transition Standards. For all countries other than the [*] Countries (“[*] Countries”), the parties will mutually agree on the quality metrics (e.g., user abandonment and aggregate click-through rate) required to transition Algorithmic Search Services for Web Internet Search, Image Internet Search and Video Internet Search (“[*] Transition Standards”). For any country, following the date that Microsoft demonstrates that it has satisfied each applicable test (i.e., the [*] Transition Standards for [*] Countries and the applicable [*] Transition Standards for each [*] Country) and is capable of meeting the SLA within such country (the “Test Passage Date”...