Quality of production Sample Clauses

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
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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. 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

Related to Quality of production

  • Supply of Product Salix shall use reasonable efforts to supply the Product during the Co-Promotion Period in sufficient quantities to satisfy the levels of Product sales forecasted in the then current Marketing Plan. Salix shall maintain reasonable inventory levels of the Product in order to ensure their ability to fulfill this obligation. Salix shall have the sole responsibility and right to fill orders with respect to the Product. Altana shall not solicit orders for the Product but, if for any reason, Altana shall receive an order for the Product, Altana shall promptly forward to Salix any such orders. All orders for Product shall be subject to acceptance by Salix, in its sole discretion, which acceptance shall not be unreasonably withheld. Salix may cancel any order for Product at any time after acceptance without incurring any liability to Altana. Salix shall be solely responsible for responding to requests from Target Physicians for individual patients who need the Product but are unable to afford it. Any such request shall be forwarded by Altana to Salix for processing. Salix shall have the sole right and responsibility for establishing and modifying the terms and conditions of the sale of the Product, including (a) the price at which the Product will be sold, (b) whether the Product will be subject to trade or quantity discounts, (c) whether any discount will be provided for payments on accounts receivable, (d) whether the Product will be subject to rebates, returns and allowances or retroactive price reductions, (e) the channels of distribution of the Product, and (f) whether credit [*] Confidential treatment requested; certain information omitted and filed separately with the SEC. is to be granted or refused in connection with any sale of Product. In the event that Salix fails to supply the Product as required pursuant to this Agreement for any reason other than a Force Majeure, which such failure results in lost sales for Altana, the Parties shall meet and attempt to negotiate a mutually agreeable and commercially reasonable solution. If the Parties cannot reach such an agreement within a reasonable period of time, the issue will be dealt with as contemplated under Section 4.4 of this Agreement.

  • Development of Products (a) During the term of this Agreement, ViewRay may from time to time seek services from PEKO with respect to the development of certain Products that can be incorporated into the ViewRay Renaissance™ MRI-guided radiation therapy system. For each Program to be undertaken by PEKO pursuant to this Agreement, the parties will prepare a “Work Statement” and agree to said “Work Statement” in substantially the form attached as Attachment 1. Each Work Statement will describe: (i) the (i) services that PEKO will be responsible for providing to ViewRay and the deliverables that PEKO will be responsible for delivering to ViewRay (“Deliverable(s)”), (ii) delivery schedule for the Deliverables, (iii) pricing terms, (iv) work plan for the Program, and (v) ViewRay’s responsibilities in connection with the Program. Each Work Statement will be prepared based upon the requirements and information provided to PEKO by ViewRay. A separate Work Statement will be required for each Program; and each Work Statement will become subject to this Agreement only when mutually agreed and signed by ViewRay and PEKO.

  • 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 Product Prior to commercialization of the Product, the Parties may, if appropriate for both parties, negotiate in good faith a manufacturing and supply agreement to provide for Licensor to fulfill the manufacturing requirements of Licensee for Product for sale in the European market. The cost of such manufacturing shall not be greater than * percent (*%) of the cost of any competitor cGMP contract manufacturing facility that proposes to manufacturer the Product for Licensee. * Confidential information has been omitted and filed confidentially with the Securities and Exchange Commission.

  • 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.

  • 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 Services (a) The Consultant shall be responsible for the professional quality, technical accuracy, and the coordination of all designs, drawings, specifications, and other services furnished pursuant to this Agreement.

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