Quality of production Sample Clauses

Quality of production. The material in use must meet the following standard specifications and requirements: Standards, requirements Standard headers EN 10204 • Inspection certificate 3.1B or after consultation with Scheuerle 2.3 also 2.2 (only for quenched and tempered, case hardening and/or hardened steels) “Material test certificates” EN 10163 Part 2 • Class B, subassembly 3 EN 10163 Part 3 • Class D, subassembly 3 Delivery requirements for surface conditions of hot-rolled steel products EN 10083 Part 2 Quenched and tempered steels: Technical delivery conditions DIN 17210 Hardening steels: Technical delivery conditions DIN ISO 2768 mK For non-tolerated dimensions and angles DIN ISO 1302 Surface roughness All important features on the drawing or in the order (such as tolerated dimensions, test dimensions, shape and position tolerances) must be 100% tested and entered on a test report. Test reports must be able to be assigned to components (e.g. serial number, build number, etc.). For the tests, only calibrated test equipment is to be used. The TII Group reserves the right to perform sample testing of the test equipment used. For parts made of quenched and tempered steel or hardened steel or with hardened parts in general, the actual value of the strength (N/mm²) and the measured hardness in the scale specified on the drawing (HRC, HB, etc.) must be entered on the measurement report. If provision is made for a xxxx on the drawing or in the order, the parts are to be marked at the specified position according to the instructions (company emblem/week/year/consecutive build number).
Sample 1
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Quality of production. The technical quality of the completed production elements shall be equal to the quality requirements customarily required by US network animation broadcasters. The Series shall be originally recorded in the English language, shall have the sound, music and effects fully synchronized to the applicable visual elements and shall be produced in compliance with all applicable US standards, laws and regulations, including (without limitation) broadcast standards, privacy, publicity, intellectual property and copyright laws.
Sample 1
Quality of production. All important inspection characteristics on the drawing or in the order (e.g. tolerated dimensions, inspection dimensions, form and position tolerances) must be completely inspected and entered in an inspection log. Inspection logs must be assignable to components (e.g. serial number, construction number etc.). Only calibrated test equipment shall be used for the tests. The TII Group reserves the right to carry out sample checks on the test equipment used. In the case of components made of quenched and tempered steel, case-hardened steel or hardened parts in general, the actual value of the strength (N/mm²) or the measured hardness in the scale indicated on the drawing (HRC, HB etc.) must also be entered in the measurement protocol. If a marking is provided on the drawing or if it is specified in the order, the parts are to be marked at the specified place according to the regulations (company logo/week/year/consecutive construction number).
Sample 1
Quality of production. Publisher shall not, however, be responsible in any manner whatsoever for imperfect color reproductions resulting from poor quality transparencies or any imperfections in transparencies of artwork. Publisher shall comply with all editorial adjacency guidelines provided by Client. Publisher shall ensure that Client’s ad will not appear adjacent to advertisements for the following destinations/CVBs: Las Vegas, Chicago, Atlanta, Dallas, Denver, Washington DC, Visit Florida, Miami, Tampa, Nashville, California, Los Angeles, and San Francisco. Publisher shall ensure that ads are placed in the exact location specified in the corresponding Insertion Order. Publisher may not modify the location of ads without obtaining Client’s prior approval in writing. Such approval may be granted or denied in Client’s sole discretion.
Sample 1

Related to Quality of production

  • Conformity of production The conformity of production procedures shall comply with those set out in the Agreement, Appendix 2 (E/ECE/324-E/ECE/TRANS/505/Rev.2), with the following requirements:

  • Supply of Product 3.1 In accordance with the terms of this Agreement, GENSIA SICOR (through SICOR) shall supply all of PURCHASER'S ordered requirements for Product in bulk form for use by PURCHASER in the Territories in accordance with the provisions of this Agreement. The right and license of PURCHASER to obtain, use and distribute Product (including, without limitation, the right to make or have made Product) from GENSIA SICOR and SICOR shall be (i) non-exclusive in the Non-exclusive Territory, and (ii exclusive in the Exclusive Territory; provided, however, that the rights and licenses set forth in clause (ii) above shall be co-exclusive in each jurisdiction in which GENSIA SICOR (or ALCO or SICOR, as the case may be) has binding written agreements, or binding written commitments that will lead to binding written agreements, to sell Product on the Restatement Date (which is limited to only those [ * ] and the [ * ] with whom GENSIA SICOR has commitments that are in existence on the Restatement Date), but only with respect to such third parties and only until the earlier of expiration or termination of such agreements; and provided, further that GENSIA SICOR shall use all diligent efforts (without any obligation to violate or alter the terms of such agreements existing on the Restatement Date) to provide PURCHASER with exclusive rights and licenses to sell the Products in the Territory as soon as possible. All Product hereunder shall be manufactured at SICOR's GMP facilities at Rho, Italy, the facility identified in Exhibit 9 hereto, the Santxx Xxxility and additional (as necessary and as provided in Section 6 below) GMP qualified facilities that are approved in advance by PURCHASER (which approval will not be unreasonably withheld). In addition, all Product shall be manufactured (A) in accordance with drug substance manufacturing and quality control procedures existing on the Effective Date, which drug substance manufacturing and quality control procedures have been included in manufacturer's Abbreviated Antibiotic Drug Application ("AADA") submitted to the FDA in 1996, and that will be submitted to other Regulatory Authorities in the Territory (which AADA shall include at least the elements set forth in the Drug Master File) in accordance with U.S. FDA current Good Manufacturing Practices, and (B) to the Q/C Specifications. GENSIA SICOR shall cause SICOR to use its diligent efforts to [ * ] in order to produce and supply all Product ordered by Purchaser hereunder and to meet the Product [ * ] that will be set forth in Schedule 1 hereto within [ * ] after the Restatement Date. In addition, GENSIA SICOR agrees to the following (and GENSIA SICOR agrees to cause SICOR to undertake):

  • Supply of Products During the term of this Agreement and any extension hereof, the Seller shall sell and supply the products as set out in Schedule 1 hereto (“Products”) to SiPM and SiPM shall buy from the Seller such Products on a non-exclusive basis. The specifications of the Products are set out in Schedule 2 hereto. SUPPLY AGREEMENT - SiPM A Supply Agreement is a document between two parties, a Supplier and a Purchaser. The Supplier can be an individual or business and is the party that " supplies," or sells, the goods to the Purchaser. The Purchaser can also be an individual or a business and is the party that purchases for its use the goods that the Supplier provides.

  • Quality of Work Consultant agrees that all Services performed under this Agreement will conform to the specifications of the College, be free from errors, and be of professional quality according to applicable industry standards. Upon notice by the College, Consultant will promptly correct any defects without charge to the College unless the request is considered new work by both parties.

  • Marketing of Production Except for contracts listed and in effect on the date hereof on Schedule 7.19, and thereafter either disclosed in writing to the Administrative Agent or included in the most recently delivered Reserve Report (with respect to all of which contracts the Borrower represents that it or its Subsidiaries are receiving a price for all production sold thereunder which is computed substantially in accordance with the terms of the relevant contract and are not having deliveries curtailed substantially below the subject Property’s delivery capacity), no material agreements exist which are not cancelable on 60 days notice or less without penalty or detriment for the sale of production from the Borrower’s or its Subsidiaries’ Hydrocarbons (including, without limitation, calls on or other rights to purchase, production, whether or not the same are currently being exercised) that (a) pertain to the sale of production at a fixed price and (b) have a maturity or expiry date of longer than six (6) months from the date hereof.

  • Manufacture of Products All Products marketed through Grantor's Web ------------------------- Site shall be manufactured, packaged, prepared, and shipped in accordance with the specifications and requirements described on Exhibit A hereto as it may be modified from time to time. Quality control standards relating to the Product's weight, color, consistency, micro-biological content, labeling and packaging are also set forth on Exhibit A. In the event that Exhibit A is incomplete, Products shall be manufactured and shipped in accordance with industry standards.

  • Quality Specifications SANMINA-SCI shall comply with the quality specifications set forth in its Quality Manual, incorporated by reference herein, a copy of which is available from SANMINA-SCI upon request.

  • QUALITY OF GOODS 5.1 The Supplier warrants that on delivery, and for a period of 12 months from the date of delivery (warranty period), the Goods shall:

  • 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.

  • Quality of Materials and Workmanship Unless otherwise specified, all materials shall be new, and both workmanship and materials shall be of good quality. The Contractor shall, if required, furnish satisfactory evidence as to the kind and quality of materials and work. The burden of proof is on the Contractor.

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