Design and Manufacture Sample Clauses

Design and Manufacture. METROLOGIC shall design, manufacture, and deliver Alpha Units, Beta Units, and Pilot Units of Modified METROLOGIC Qualifying Product and/or Modified Elected New METROLOGIC Product, as applicable, to SYMBOL upon the receipt of a purchase Order therefor.
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Design and Manufacture. 10.1. The supplier shall be entitled to claim the usual tolerances customary in the trade on all dimensions. 10.2. If no detailed drawings or specifications are provided by the customer, the requirements shall be agreed between the parties in writing. 10.3. Any change to the design or form of any goods shall be agreed between the parties in writing.
Design and Manufacture. 6.1.1. The Supplier shall design and manufacture the Equipment strictly in compliance with the Technical Requirements and any further written instructions of the IAA. 6.1.2. A special attention will be brought, inter alia, to the requested dimensions of the Equipment and its requested material and/or electrical characteristics, bearing in mind that the Equipment shall be designed to meet the specific professional needs of the IAA’s employees and interface, inter alia (and without limiting) with the IAA infrastructures and Supported Technologies, all as described in the Technical Requirements (the “Interface Requirements”). 6.1.3. All costs and expenses related to the design and manufacture shall be comprised in the Consideration to be paid to the Supplier, as stipulated in Section 7 below. 6.1.4. The Supplier declares and agrees that it thoroughly and carefully examined the Technical Requirements and hereby represents that the Equipment will fully comply therewith and with the instructions of the IAA from time to time and that the Products will be fully compatible with the infrastructures of the IAA and with the Supported Technologies. 6.1.5. The Supplier acknowledges that the IAA is entitled to reject the Equipment in virtue of its right of rejection stipulated in Section 6.6 below should it appear, after delivery of the Equipment, that the latter does not meet the Technical Requirements or the IAA’s written instructions, and specifically if it appears that the Interface Requirements have not been met or duly taken into account, as expressly stipulated in the Technical Requirements. 6.1.6. The Supplier undertakes to meet each and every milestone detailed in Section 6 of the Technical Specifications with regard to the design of the Products.
Design and Manufacture. 23.1. GRW shall be entitled to claim the usual tolerances customary in the trade on all dimensions. 23.2. If no detailed drawings or specifications are provided by the CUSTOMER, GRW shall be entitled in its sole discretion to interpret the requirements of the CUSTOMER and its decision shall be final and binding on the CUSTOMER. 23.3. GRW reserves the right to make any reasonable change to the design or form of any goods provided that the state of performance and quality and specifications remain materially unaffected.
Design and Manufacture. SELLER shall design, customize, and manufacture the modular swimming pool delivered to BUYER.
Design and Manufacture. 6.2.1. The Supplier shall design, and manufacture the Products and the Spare Parts strictly in compliance with the SOW, attached hereto as Annex A, and any further written instructions of the IAA. 6.2.2. All costs and expenses related to the design and manufacture shall be comprised in the Consideration to be paid to the Supplier, as stipulated in Section 7 below. 6.2.3. The Supplier declares and agrees that it thoroughly and carefully examined the SOW and hereby represents that the Products and the Spare Parts will fully comply therewith and with the instructions of the IAA from time to time. 6.2.4. The Supplier acknowledges that the IAA is entitled to reject the Products and/or the Spare Parts in virtue of its right of rejection stipulated in Section 6.6 below should it appear, after delivery of the Products and/or the Spare Parts, that the latter does not meet the SOW or the IAA’s written instructions.
Design and Manufacture 
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Related to Design and Manufacture

  • 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.

  • 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.

  • Equipment and Materials CONTRACTOR shall provide all equipment, materials, and supplies necessary for the performance on the Agreement except:

  • Personnel Equipment and Material Engineer shall furnish and maintain, at its own expense, quarters for the performance of all Engineering Services, and adequate and sufficient personnel and equipment to perform the Engineering Services as required. All employees of Engineer shall have such knowledge and experience as will enable them to perform the duties assigned to them. Any employee of Engineer who, in the reasonable opinion of County, is incompetent or whose conduct becomes detrimental to the Engineering Services shall immediately be removed from association with the Project when so instructed by County. Engineer certifies that it presently has adequate qualified personnel in its employment for performance of the Engineering Services required under this Contract, or will obtain such personnel from sources other than County. Engineer may not change the Project Manager without prior written consent of County.

  • 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.

  • Solicitations for Subcontracts, Including Procurement of Materials and Equipment In all solicitations either by competitive bidding or negotiation made by the Local Government for work to be performed under a subcontract, including procurement of materials or leases of equipment, each potential subcontractor or supplier will be notified by the Local Government of the Local Government’s obligations under this Agreement and the Acts and Regulations relative to Nondiscrimination on the grounds of race, color, or national origin.

  • Third Party Materials The Application may display, include, or make available third-party content (including data, information, applications, and other products, services, and/or materials) or provide links to third-party websites or services, including through third- party advertising ("Third-Party Materials"). You acknowledge and agree that Company is not responsible for Third-Party Materials, including their accuracy, completeness, timeliness, validity, copyright compliance, legality, decency, quality, or any other aspect thereof. Company does not assume and will not have any liability or responsibility to you or any other person or entity for any Third-Party Materials. Third-Party Materials and links thereto are provided solely as a convenience to you, and you access and use them entirely at your own risk and subject to such third parties' terms and conditions.

  • Third Party Components The Products and Services may contain third party components (including open source software) subject to separate license agreements. To the limited extent a third party license expressly supersedes this XXXX, such third party license governs Customer’s use of that third party component.

  • Manufacturing Technology Transfer Upon AbbVie’s written request with respect to a given Collaboration CAR-T Product and Licensed Product, Caribou shall effect a full transfer to AbbVie or its designee (which designee may be an Affiliate or a Third Party Provider) of all Materials and Know-How Controlled by Caribou relating to the then-current process for the Manufacture of such Collaboration CAR-T Product and any corresponding Licensed Products (each, a “Manufacturing Process”). Caribou shall provide, shall cause its Affiliates to provide, and shall use Commercially Reasonable Efforts to assist AbbVie in causing all Third Party Providers to provide, all reasonable assistance requested by AbbVie to enable AbbVie (or its Affiliate or designated Third Party Provider, as applicable) to implement each Manufacturing Process at the facilities designated by AbbVie. If requested by AbbVie, such assistance shall include facilitating the entering into of agreements with applicable Third Party suppliers relating to such Collaboration CAR-T Product and any corresponding Licensed Products. Without limitation of the foregoing, in connection with the Manufacturing Process and related transfer: (a) Caribou shall, and shall cause its Affiliates to, make available to AbbVie (or its Affiliate or designated Third Party Provider, as applicable), and shall use Commercially Reasonable Efforts to assist AbbVie in causing all Third Party Providers to make available to AbbVie, from time to time as AbbVie may request, all Materials and Manufacturing-related Know-How Controlled by Caribou relating to each Manufacturing Process, including methods, reagents and processes and testing/characterization Know-How, and all documentation constituting material support, performance advice, shop practice, standard operating procedures, specifications as to Materials to be used, and control methods, that are necessary or reasonably useful to enable AbbVie (or its Affiliate or designated Third Party manufacturer, as applicable) to use and practice such Manufacturing Process; (b) Caribou shall cause all appropriate employees and representatives of Caribou and its Affiliates, and shall use Commercially Reasonable Efforts to assist AbbVie in causing all appropriate employees and representatives of Third Party Providers, to meet with employees or representatives of AbbVie (or its Affiliate or designated Third Party Provider, as applicable) at the applicable manufacturing facility at mutually convenient times to assist with the working up and use of each Manufacturing Process and with the training of the personnel of AbbVie (or its Affiliate or designated Third Party Provider, as applicable) to the extent necessary or reasonably useful to enable AbbVie (or its Affiliate or designated Third Party Provider, as applicable) to use and practice such Manufacturing Process; (c) Without limiting the generality of this Section 4.4.2, Caribou shall cause all appropriate analytical and quality control laboratory employees and representatives of Caribou and its Affiliates, and shall use Commercially Reasonable Efforts to assist AbbVie in causing all appropriate analytical and quality control laboratory employees and representatives of Third Party Providers, to meet with employees or representatives of AbbVie (or its Affiliate or designated Third Party Provider, as applicable) at the applicable manufacturing facility and make available all necessary equipment, at mutually convenient times, to support and execute the provision of all applicable analytical methods and the validation thereof (including all applicable Know-How, Information and Materials Controlled by Caribou, and sufficient supplies of all primary and other reference standards); (d) Caribou shall, and shall cause its Affiliates to, take such steps, and shall use Commercially Reasonable Efforts to assist AbbVie in causing Third Party Providers take such steps, as are necessary or reasonably useful to assist AbbVie (or its Affiliate or designated Third Party Provider, as applicable) in obtaining any necessary licenses, permits or approvals from Regulatory Authorities with respect to the Manufacture of the applicable Collaboration CAR-T Products and corresponding Licensed Products at the applicable facilities; and (e) Caribou shall, and shall cause its Affiliates to, provide, and shall use Commercially Reasonable Efforts to assist AbbVie in causing Third Party Providers to provide, such other assistance as AbbVie (or its Affiliate or designated Third Party Provider, as applicable) may reasonably request to enable AbbVie (or its Affiliate or designated Third Party Provider, as applicable) to use and practice each Manufacturing Process and otherwise to Manufacture the applicable Collaboration CAR-T Products and corresponding Licensed Products.

  • PRODUCT MANUFACTURER'S SUPPLIERS Only those dealers/distributors listed by the manufacturer will be considered authorized to act on behalf of the Product Manufacturer.

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