Design and Manufacturing Sample Clauses

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Design and Manufacturing. QVC and the Company will cooperate and work in concert to develop designs (“Designs”) and prototypes (“Prototypes”) for the manufacture of the Products and Co-Branded Products. Company and Mizrahi or, in the event of (A) the death of Mizrahi or (B) the disability of Mizrahi, and the election of QVC not to terminate this Agreement pursuant to paragraph 6(c) in the event of either occurrence, a substitute designer mutually acceptable to Company and QVC, shall provide no fewer than 200 Designs to QVC during each License Period Year (as defined in paragraph 2(g) below) of the License Period. Prior to the manufacture of any specific Product line or Co-Branded Product line (each Product line or Co-Branded Product line, an “Item”), QVC will provide a production quality sample (each, a “Sample”) of each Item for the Company’s approval. Each Item produced, if any, by a Manufacturer will be an accurate reproduction in all material respects to the Sample. Further, the Company shall notify QVC of its approval or disapproval of any Sample within five (5) Business Days (as defined below) after Company receives such Sample. The parties will reasonably cooperate in an attempt to resolve any disapproval of, objections to or concerns with, the Sample. If, however, the Company fails to disapprove any Sample within five (5) Business Days of its receipt of such Sample, Company will be deemed to have approved such Sample. Company and Mizrahi acknowledge that as between them and QVC, QVC owns the Designs. “Business Day”, as used herein, shall mean any day except Saturday, Sunday and/or any other day on which commercial banks in Philadelphia, Pennsylvania or New York, New York are authorized by law to close.
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Design and Manufacturing. 9 6.1 Seasonal Design, Time and Action Calendar…………………………………………..9 6.2 Overall Commitment to Quality…………………………………………………………..9 6.3 Samples of Manufactured Products……………………………………………………..9
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Design and Manufacturing. 9 6.1 Seasonal Design, Time and Action Calendar…………………………………………..9 6.2 Overall Commitment to Quality…………………………………………………………..9 6.3 Samples of Manufactured Products……………………………………………………..9 6.4 Non-Conforming Products……………………………………………………………......9 6.5 Withdrawal of Approval……………………………………………..………………..….10 6.6 Assistance by Licensor………..………………………………………………………....10 6.7 Ownership of Designs…………………………………………………………………….11 6.8 Cost of Designs, Samples………………………………………………………………...11 6.9 Code of Conduct…………………………………………………………………………..11 6.10 Monitoring Program……………………………………………………………………...12 6.11 Third Party Manufacturing Agreement………………………………………………...12 6.12 Information About Third Party Manufacturers, ………………………………………12 6.13 Inspection of Facilities…………………………………………………………………...13 6.14 Compliance with Applicable Laws- Generally.…………………………………...…….13 6.15 Notice on Invoices………………………………………………………………….…….14 6.16 Meetings……………………………………………………………………………..…….14 6.17 Anti-Counterfeiting………………………………………………………………….……14 ARTICLE 7. BRAND DEVELOPMENT, SALES AND MARKETING 14 7.1 Best Efforts……………………………………………………………………………….....14 7.2 Sales and Deliveries…………………………………………………………………….......15 7.3 Reporting………………………………………………………………………………….....15 7.4 Sales/Marketing Plans ........………………………………………………………….....…15 7.5 Minimum Sales Levels………………………………………………………………….......15 7.6 Certain Sales Excluded…………………………………………………………………......15 7.7 Approved Customers……………………………………………………………………....16 7.8 Prohibited Sales………………………………………………………………………….....16 7.9 Showrooms and In-Store Shops………………………………………………………….17 7.10 Products for Licensor’s Use……………………………………………………………..17 7.11 Purchases By Licensor…………………………………………………………………...17 7.12 Purchases By Outlet Stores Owned or Operated by Licensor or its Affiliates……..18 7.13 Purchases By ▇▇▇▇▇ ▇▇▇▇▇▇▇▇ Stores, Websites and Franchisees…………………..18 7.14 Disposal of Off-Price Products…………………………………………………………..18 7.15 Penalties for Unapproved and Prohibited Sales……………………………………….19 ARTICLE 8. ADVERTISING 20 8.1 Guaranteed Minimum and Brand Advertising Payments………………………………20 8.2 Percentage Advertising Payment………………………………………………………...20 8.3 Media Plan and Licensor’s Advertising Spending……………………………………..21 8.4 Approval of Labels and Licensee’s Advertising……………………………………….22 8.5 Launch…………………………………………………………………………………...….22 8.6 Branded Shows………………………………………………………………………….....22 8.7 Trade Shows……………………………………………………………………………......23 8.8 Public Announcements…………………………………………………………………....23 ARTICLE 9. R...
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Design and Manufacturing. 3.1 SUPPLIER undertakes that Products, Parts and Packaging are designed and manufactured to comply with the objectives of the Waste Electrical and Electronic Equipment Directive (WEEE) (2002/96/EC). 3.2 Upon request, SUPPLIER will provide PMS with environmentally-related information regarding all materials included in the Products, Parts and Packaging including as a minimum: 3.2.1 Necessary information for disassembling, recycling, reusing and treating Products, Parts and Packaging at end of life; 3.2.2 The location of dangerous substances and preparations in Products, Parts and Packaging; 3.2.3 Appropriate markings in accordance with the WEEE Directive requirements. 3.3 On the basis of best effort, SUPPLIER undertakes to participate in Philips’ and/or BUYER’s environmental programs, such as 3.3.1 Reduction of the weight and volume of Packaging and Packaging materials to as low as possible and to the technically necessary minimum, while maintaining basic Packaging functions including transportability, protection and communication of information; 3.3.2 Environmentally Conscious Design (EcoDesign), i.e., reducing the integral environmental impact of the product over its entire life cycle; 3.3.3 Reusability of Products, Parts and Packaging.
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Design and Manufacturing. VEW and Syratech shall collaborate with respect to all aspects of merchandising and product development for the Licensed Property in order to take maximum advantage of each Party’s expertise, provided that all aspects of the design of the Licensed Property shall be subject to VEW’s approval, and Syratech shall not manufacture any pre-production sample, production sample or item of Licensed Property hereunder without VEW’s approval. Subject to the immediately preceding sentence, the design and manufacturing process hereunder with respect to items of Licensed Property shall be as follows:
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Design and Manufacturing. ID No. Key Question short description Standards of reference
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Design and Manufacturing 
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Related to Design and Manufacturing

  • 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. (b) The Supplier shall not change any process, material, component, packaging or manufacturing location without the Purchaser’s express prior written approval.

  • Development Work The Support Standards do not include development work either (i) on software not licensed from CentralSquare or (ii) development work for enhancements or features that are outside the documented functionality of the Solutions, except such work as may be specifically purchased and outlined in Exhibit 1. CentralSquare retains all Intellectual Property Rights in development work performed and Customer may request consulting and development work from CentralSquare as a separate billable service.

  • Manufacturing Technology Transfer Except as provided in Section 4.3(f)(iii)(1) and Section 6.10, with respect to any Collaboration Product (or LGC Reserved Product, if applicable) for which LGC (or its Affiliate) performed CMC Development or CMC Manufacturing, if (a) Cue does not elect for LGC to perform CMC Step 2, CMC Step 3, or CMC Step 4 (or with respect to LGC Reserved Products, upon completion of CMC Step 1), or (b) upon failure of the Parties to reach agreement with respect to a Clinical Supply Agreement or a Commercial Supply Agreement or (c) [***] under this Agreement and does not cure such breach within [***] days (provided, that if such breach is not reasonably capable of cure within such [***] day period, then such cure period shall be automatically extended for an additional [***] day period as long as LGC continues to use diligent efforts to cure such breach in accordance with a reasonable cure plan and if such breach is not reasonably capable of cure within such combined [***] day period, then Cue shall reasonably consider consenting to any extension of such cure period as long as LGC continues to use diligent efforts to cure such breach in accordance with a reasonable cure plan), as applicable, then, in each case upon the written request of Cue, LGC shall use Commercially Reasonable Efforts to make a technology transfer to an Approved CMO the Manufacturing processes (including materials and such other information) but solely as is necessary to enable the Manufacture of such Collaboration Product (including the Collaboration Compound therein) (or LGC Reserved Product, including the LGC Reserved Compound therein, if applicable) by such Approved CMO to comparable biochemical structure, quality and purity as that Manufactured by LGC or its Affiliate or CMO, provided that neither Cue, LGC or any Third Party shall perform such a technology transfer to any CMO [***] without LGC’s consent, not to be unreasonably withheld, conditioned or delayed if LGC has approved the CMO to manufacture Collaboration Products (or LGC Reserved Products, if applicable). LGC shall conduct such technology transfer as soon as reasonably practicable after receiving such written notice, using good faith efforts to support supply needed to achieve timelines in the Cue Territory Development Plan (or Cue’s development plan for LGC Reserved Products, if applicable) or Cue Territory Commercialization Plan, as applicable. LGC shall conduct the first technology transfer for each Collaboration Product (or LGC Reserved Products, if applicable) [***] (provided that [***]) for a period of up to [***] months from the date Cue or its designee has provided notice it is ready to receive the technology transfer, provided, that such [***] month period [***]. After the expiration of the initial such [***] month period for a Collaboration Product (or LGC Reserved Products, if applicable), if required to complete the technology transfer to enable the Manufacture of such Collaboration Product (including the Collaboration Compound therein) (or LGC Reserved Product, including the LGC Reserved Compound therein, if applicable) by such Approved CMO to comparable biochemical structure, quality and purity as that Manufactured by LGC, LGC shall continue to provide support to Cue for up to an additional [***] period for up to [***] hours at the FTE Rate and thereafter at [***]. Thereafter, LGC will also provide [***] for such Collaboration Product (or LGC Reserved Products, if applicable). Neither Cue nor its Affiliates or Cue Collaborators shall reverse engineer any materials provided hereunder by LGC. Notwithstanding anything in this Agreement to the contrary, LGC’s CMC information may only be shared with an Approved CMO.

  • Manufacture 2.1. The LED(s) on the LED module shall be equipped with suitable fixation elements. 2.2. The fixation elements shall be strong and firmly secured to the LED(s) and the LED module.

  • Supplier Development lf the Buyer identifies problems in supplier performance based on supplier monitoring, he shall initiate improvement measures at the Supplier. The Buyer shall pursue the possibilities of continuous improvement of the Supplier. The supplier audit is a form of supplier development; the exchange of information and experience between the Buyer and the Supplier also serves this purpose.