PRODUCT QUALITY CONTROL Sample Clauses

PRODUCT QUALITY CONTROL. 4.5.1. The Host shall have standard quality procedures at the Depot. The Products shall at the time of delivery comply with the relevant specifications as may be stipulated by the relevant institutions, including XXXXX (South African Petroleum Industry Association), which determines the XXXXX Oil Industry Product Exchange Specifications ("OIPES"); the Department of Energy, through the Petroleum Products Specifications and Standards promulgated in terms of the Petroleum Products Act, 1977 (as amended) and/or the South African Bureau of Standards' South African National Standards ("SANS"). To the extent that there is a conflict between the abovementioned Product specifications, then the OIPES specifications shall apply.
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PRODUCT QUALITY CONTROL. The District reserves the right to discontinue service of all or any portion of any contract resulting from this bid for any reason determined by the District to be detrimental to health and welfare of the students and school personnel, or failure to meet contract specifications or wholesomeness standard, and to hold the contractor in default. All products received under this contract shall be processed according to the health and sanitation standards for plant facilities and food processing established by the locality or state in which Processor’s plant is located or by the applicable federal standards, whichever is higher. The contractor shall furnish proof of an operational Hazard Analysis Critical Control Point (HACCP) plan at the time of bid submission. Also, the Contractor shall provide products from manufacturers with HACCP systems in place. Additionally, Contractor shall provide products from manufacturers requiring a State, local or Federal Environmental Services inspection, or other third party governmental agency with regulating authority and jurisdiction over product manufacturers. Contractor shall follow appropriate procedures for First in First Out (FIFO) stock rotation system. In the event of product contamination issue, Contractor shall provide trace back capabilities for all products to the point of origin. Evidence of such procedures should be submitted at the time of bid.
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PRODUCT QUALITY CONTROL. Buyer has a duty to protect the quality of ------------------------ Seller's products delivered to it by Seller or Seller's authorized distributors. Seller represents that the Mobil lubricants that it supplies under this Agreement: 1) meet applicable API standards and 2) will meet future applicable API standards.
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PRODUCT QUALITY CONTROL. 5.3.1. Both Parties will have standard quality procedures at Depots.
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PRODUCT QUALITY CONTROL. 5.4.1 The Host shall have standard quality procedures at each Depot. The Products shall at the time of delivery comply with the relevant specifications as stipulated by XXXXX (South African Petroleum Industry Association), which determines the XXXXX Oil Industry Product Exchange Specifications ("OIPES").
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PRODUCT QUALITY CONTROL. 2.1 The objectives of this Section 2 are to assure that (i) the physical and sensory characteristics of the Product brewed and packaged by Redhook will be essentially the same as the Hefeweizen beer brewed and packaged by Xxxxxx in its Portland, Oregon facility and (ii) the Product is free of any microbiological contamination.
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PRODUCT QUALITY CONTROL. Buyer has a duty to protect the quality of products delivered to it by Seller or Seller's authorized distributors.
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PRODUCT QUALITY CONTROL. 2.1 The objectives of this Section 2 are to assure that the physical and sensory characteristics of the Product manufactured and packaged by PackItGreen will be essentially the same as the Product produced by EATware and packaged by EATware in its facilities in the Far East.
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PRODUCT QUALITY CONTROL 
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Related to PRODUCT QUALITY CONTROL

  • Quality Control A. Controlled Affiliate agrees to use the Licensed Marks and Name only in connection with the licensed services and further agrees to be bound by the conditions regarding quality control shown in attached Exhibit A as they may be amended by BCBSA from time-to-time.

  • Product Quality 4.1 The following provisions shall apply to Product after Production:

  • Product Recall (a) If a recall is required by applicable Law, or if Buyer or Supplier reasonably determines that a recall is advisable because the goods may create a potential safety hazard, are not in compliance with any applicable code, standard or legal requirement, or contain a defect or non-conformance with the requirements of this Order occurring or likely to occur in multiple goods, which such defects or non-conformances are substantially similar or have substantially similar causes or effects (collectively a “Serial Defect”), the parties shall promptly communicate such facts to each other. At Buyer’s request, Supplier shall promptly develop a corrective action plan satisfactory to Buyer, which shall include all actions required to recall and/or repair the goods and any actions required by applicable Law (“Corrective Action Plan”) for Buyer’s review and approval. At Buyer’s election, Xxxxx may develop the Corrective Action Plan. In no event shall Buyer and Supplier’s failure to agree on the Corrective Action Plan delay the timely notification of a potential safety hazard, non-compliance or Serial Defect to users of the goods, cause either party to be non-compliant with applicable Law or prevent Buyer from taking reasonable actions to prevent injury or damage to persons, equipment or other property. Supplier and Buyer shall cooperate with and assist each other in any corrective actions and/or filings, if applicable.

  • 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.

  • Product Recalls The Company is not aware of any pattern or series of claims against the Company or any of its subsidiaries which reasonably could be expected to result in a generalized product recall relating to products sold by the Company or any of its subsidiaries, regardless of whether such product recall is formal, informal, voluntary or involuntary.

  • Marketing Services The Manager shall provide advice and assistance in the marketing of the Vessels, including the identification of potential customers, identification of Vessels available for charter opportunities and preparation of bids.

  • 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 [***].

  • TECHNICAL SUPPORT SERVICES 2.1 The technical support services (the "Services"): Party A agrees to provide to Party B the relevant services requested by Party B, which are specified in Exhibit 1 attached hereto ("Exhibit 1").

  • Clinical Supply Takeda will provide to Licensee[***] the amount of TAK-385 Licensed Compound or TAK-385 Licensed Products needed by Licensee to complete all Clinical Trials contemplated by the TAK-385 Development Plan (estimated by Licensee as of the Effective Date to be [***]), solely to the extent that Takeda can supply such TAK-385 [***] = Portions of this exhibit have been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment requested under 17 C.F.R. Sections 200.80(b)(4) and 230.406. Licensed Compound or TAK-385 Licensed Products (a) from its supply of TAK-385 Licensed Compound or TAK-385 Licensed Products in existence as of the Effective Date and which supply can be used for its intended purposes without further re-processing (the “Initial Clinical Supply”) and (b) after retaining the amount needed by Takeda for Clinical Trials in the Takeda Territory. Takeda will also provide to Licensee, at [***] any additional supplies of TAK-385 Licensed Compound or TAK-385 Licensed Products in excess of the Initial Clinical Supply needed by Licensee to complete all Clinical Trials contemplated by the TAK-385 Development Plan. Within [***] days after the Effective Date, the Parties will enter into a manufacturing and supply agreement (the “Takeda Clinical Manufacturing and Supply Agreement”), which will govern the terms and conditions of the Manufacturing and supply of the TAK-385 Licensed Compound and TAK-385 Licensed Products (including the Initial Clinical Supply) by Takeda to Licensee for Development purposes, including the exact quantities and the timelines for delivery. The Parties will negotiate the terms and conditions of such Takeda Clinical Manufacturing and Supply Agreement in good faith for a period of [***] days (as may be extended upon agreement of the Parties). As part of the negotiation related to the Takeda Clinical Manufacturing and Supply Agreement, the Parties shall discuss in good faith the ability of Takeda to supply to Licensee [***]. If the Parties have not entered into a definitive agreement within such negotiation period, then the final terms and conditions of such agreement will be resolved in accordance with Section 8.2 (Arbitration for Failure to Agree).

  • Support Services HP’s support services will be described in the applicable Supporting Material, which will cover the description of HP’s offering, eligibility requirements, service limitations and Customer responsibilities, as well as the Customer systems supported.

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