Quality and Packaging Sample Clauses

Quality and Packaging. 5.1. The quality of the supplied Goods must comply with the standards of the Manufacturer's plant and the country of the Manufacturer, as well as the uniform sanitary-epidemiological and hygienic requirements for the Goods on the territory of the Republic of Uzbekistan and the Republic of ___________________, technical regulations, GOST. If the Seller has transferred to the Buyer samples of the Goods, then the quality of the delivered Goods must, among other things, be no lower than the quality of the samples of the Goods previously transferred to the Buyer. 5.2. The goods must be packed in accordance with the requirements for each type of goods. The outer and inner packaging of the goods must ensure its protection during transportation from spoilage, damage, weathering and taking into account possible overloads and transshipments with proper and normal handling of the goods. 5.3. The goods must be labeled in accordance with the current legislation, contain information in accordance with the legislation of the Republic of _________________ in the field of standardization, certification, consumer protection. The marking of the goods is performed in Russian and includes the following information: country of origin, name and other data as agreed by the Parties. 5.4. Labels and counter-labels used in the manufacture of goods must correspond to the samples agreed by the parties. 5.5. If the supplied Goods are subject to the conformity assessment procedure or other legalization at the Buyer’s place of origin, then the Seller, at the Buyer’s request, undertakes at his own expense to provide the required number of samples of the Goods, as well as the necessary documents for the Goods in accordance with the legislation in force at the location of the Buyer, the moment of the start of deliveries. The Parties agreed to consider this condition an essential condition of this Contract.
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Quality and Packaging. (a) The Licensee warrants that: (i) the Licensed Commodities will be of good quality, design, material and workmanship; (ii) the Licensed Commodities will be suitable for their intended purpose; (iii) no injurious, deleterious or toxic substances will be used in or on the Licensed Commodities; (iv) the Licensed Commodities will not cause harm when used as instructed and with ordinary care for their intended purpose; and (v) the Licensed Commodities will be manufactured, sold and distributed in strict compliance with all applicable laws and regulations.
Sample 1
Quality and Packaging. 7.1 The Supplier warrants that on delivery or collection, and for a period of 3 months from the date of delivery or collection (Warranty Period), the Goods (including its packaging) shall: 7.1.1 conform in all material respects with the Specification (where applicable); and 7.1.2 be free from material defects in design, material and workmanship; and 7.1.3 be of merchantable quality (within the meaning of the Sale of Goods Act 1980); 7.1.4 be fit for any purpose held out by the Supplier. 7.2 Subject to clause 7.1, if: 7.2.1 the Customer gives notice in writing to the Supplier during the Warranty Period within a reasonable time of discovery that some or all of the Goods do not comply with the warranty set out in clause 7.1; 7.2.2 the Supplier is given a reasonable opportunity of examining such Goods; and 7.2.3 the Customer (if asked to do so by the Supplier) returns such Goods to the Supplier's place of business at the Customer's cost, the Supplier shall, at its option, replace the defective Goods, or refund the price of the defective Goods in full. 7.3 The Supplier shall not be liable for the Goods' failure to comply with the warranty set out in clause 7.1 if: 7.3.1 the Customer makes any further use of such Goods after giving notice in accordance with clause 7.2; 7.3.2 the defect arises because the Customer failed to follow the Supplier's oral or written instructions as to the storage, commissioning, installation, use and maintenance of the Goods or (if there are none) good trade practice regarding the same; 7.3.3 the defect arises as a result of the Supplier following any drawing, design or Specification (where applicable) supplied by the Customer; 7.3.4 the Customer alters or repairs such Goods without the written consent of the Supplier; 7.3.5 the defect arises as a result of fair wear and tear, wilful damage, negligence, or abnormal storage or working conditions; or 7.3.6 the Goods differ from the Specification (where applicable) as a result of changes made to ensure they comply with applicable statutory or regulatory requirements. 7.4 Except as provided in this clause 7, the Supplier shall have no liability to the Customer in respect of the Goods' failure to comply with the warranty set out in clause 7.1. 7.5 The terms implied by sections 13 to 15 of the Sale of Goods Act 1893 are, to the fullest extent permitted by law, excluded from the Contract. 7.6 These Conditions shall apply to any repaired or replacement Goods supplied by the Supplier.
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Quality and Packaging 
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Related to Quality and Packaging

  • 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.

  • Packaging Tangible product shall be securely and properly packed for shipment, storage, and stocking in appropriate, clearly labeled, shipping containers and according to accepted commercial practice, without extra charge for packing materials, cases, or other types of containers. All containers and packaging shall become and remain Customer’s property.

  • API If the Software offers integration capabilities via an API, your use of the API may be subject to additional costs or Sage specific policies and terms and conditions (which shall prevail in relation to your use of the API). You may not access or use the API in any way that could cause damage to us or the Software, or in contravention of any applicable laws. We reserve the right in our sole discretion, to: (i) update any API from time to time; (ii) place limitations around your use of any API; and (iii) deny you access to any API in the event of misuse by you or to otherwise protect our legitimate interests.

  • Labelling The distributor, on behalf of the selected vendor agrees that all supplies of articles should invariably contain the following information on its label and the carton. One information should not be overlapped by any other information needed to be furnished. The label should contain : a. Name of the item as approved b. CMS Cat. No. c. Manufacturing date/Import date for the imported items. d. Expiry Date. (where applicable) e. Name & address of Registered Office of Manufacturers and place of manufacture. f. Manufacturing License Number. (where applicable for Manufactures) g. Batch Number (where applicable) h. Month and Year of supply. i. The label & Carton must invariably marked “W B. GOVT SUPPLY : NOT FOR SALE”. j. All Surgical items quoted/supplied by the tenderer must conform to IS /BIS /CE/USFDA. Pacemker must conform to CE & US FDA norms. In case of Drugs items quoted /supplied by tenderer MUST CONFORM TO IP, BP, or USP norms and N.F.I. –III specification as noted against the item(s) in catalogue as applicable. k. The MRP and Trade Name will not be allowed to be printed in any pack. This will lead to cancellation of candidature straightaway. However, for excisable products, insertion of writing of Govt MRP is allowed as per provision laid down in the order of the Central Excise dept. However, for imported item(s), MRP and Trade name may be allowed in addition to Generic name.

  • Labeling Upon request, Lessee will xxxx the Equipment indicating Lessor's interest with labels provided by Lessor. Lessee will keep all Equipment free from any other marking or labeling which might be interpreted as a claim of ownership.

  • Product Labeling The labeling of all Licensed Products sold or offered for sale under this Agreement shall expressly state that the Licensed Product is manufactured under a license from the Medicines Patent Pool.

  • Marketing Materials (a) During the term of this Agreement, the Sub-Adviser agrees to furnish the Manager at its principal office for prior review and approval by the Manager all written and/or printed materials, including but not limited to, PowerPointÒ or slide presentations, news releases, advertisements, brochures, fact sheets and other promotional, informational or marketing materials (the “Marketing Materials”) for internal use or public dissemination, that are produced or are for use or reference by the Sub-Adviser, its affiliates or other designees, broker-dealers or the public in connection with the Series, and Sub-Adviser shall not use any such materials if the Manager reasonably objects in writing within five business days (or such other period as may be mutually agreed) after receipt thereof. Marketing Materials may be furnished to the Manager by first class or overnight mail, facsimile transmission equipment, electronic delivery or hand delivery. (b) During the term of this Agreement, the Manager agrees to furnish the Sub-Adviser at its principal office all prospectuses, proxy statements, reports to shareholders, or Marketing Materials prepared for distribution to shareholders of each Series, or the public that refer to the Sub-Adviser in any way, prior to the use thereof, and the Manager shall not use any such materials if the Sub-Adviser reasonably objects in writing within five business days (or such other period as may be mutually agreed) after receipt thereof. The Sub-Adviser’s right to object to such materials is limited to the portions of such materials that expressly relate to the Sub-Adviser, its services and its clients. The Manager agrees to use its reasonable best efforts to ensure that materials prepared by its employees or agents or its affiliates that refer to the Sub-Adviser or its clients in any way are consistent with those materials previously approved by the Sub-Adviser as referenced in the first sentence of this paragraph. Marketing Materials may be furnished to the Sub-Adviser by first class or overnight mail, facsimile transmission equipment, electronic delivery or hand delivery.

  • Packaging Materials and Containers for Retail Sale 1. When packaging materials and containers in which a good is packaged for retail sales are classified in the Harmonized System with the good, they shall not be taken into account in determining whether all non-originating materials used in the production of the good undergo the applicable change in tariff classification set out in Annex 4.03. 2. When the good is subject to a requirement of regional value content, the value of these packaging materials and containers shall be taken into account as originating or non-originating materials, as the case may be, in calculating the regional value content of the good.

  • ODUF Packing Specifications 6.3.1 A pack will contain a minimum of one message record or a maximum of 99,999 message records plus a pack header record and a pack trailer record. One transmission can contain a maximum of 99 packs and a minimum of one pack.

  • Training Materials Training Materials will be provided for each student. Training Materials may be used only for either (i) the individual student’s reference during Boeing provided training and for review thereafter or (ii) Customer’s provision of training to individuals directly employed by the Customer.

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