Product Specifications; Packaging and Labeling Sample Clauses

Product Specifications; Packaging and Labeling. All Products delivered by Seller hereunder shall be in full compliance with the Specifications therefor and shall be ready for end-user sale, including all packaging, labeling, instructions-for-use and sterilization set forth therein, as amended. All Products shall be labeled (including bar coding/UPN numbers) in accordance with the work instructions, procedures and label text/graphics specified in writing from time to time by Buyer and mutually approved by Buyer and Seller. Buyer shall give Seller at least ** ** advance written notice of any change to its labeling procedures prior to the date when such changes are to take affect. Notwithstanding anything in this Agreement to the contrary, Buyer shall pay Seller for ** ** Reimbursements, as set forth in Section 2.3 above. All Products will be marked to make it clear that they have been manufactured by Seller and are being distributed by Buyer. Buyer may include Product as a component in any kit or collection of products. Buyer maintains the right to over-label Products as it deems necessary or appropriate in accordance with work instructions, procedures, and label text/graphics, which are mutually approved by both Parties hereto. Seller is not responsible for any over-labeling or any consequences thereof. As used in this Agreement, “Specifications” for the Product means the specifications set forth on Exhibit A, as revised from time to time pursuant to the next sentence, and as provided by Seller and approved by Buyer, including the part number, revision level, controlled drawing, and packaging and sterilization instructions for the Product and all requirements of any applicable laws and regulations of the Regulatory Authorities, specified therein. The Parties understand that the Specifications may need to be revised from time to time up to the Product Launch Date. Each version (each, a “Revision Level”) of the Specifications will be labeled with a Revision Level number (“Revision Level Number”), starting with “A-1,” and continuing sequentially with “A-2,” “A-3,” etc., and each revision of the Specifications will be so labeled and attached to this Agreement. Each subsequent Revision Level will replace and supersede all former Revision Levels for all purposes hereunder, except with respect to Article 4 of this Agreement. Attached to this Agreement as Exhibit A as of the Effective Date is Revision Level “A-1.”
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Product Specifications; Packaging and Labeling. All Company Product delivered by Supplier hereunder shall be in full compliance with Product Specifications, shall be labeled specifically for BioForm, and shall be ready for end-user sale, including all packaging, labeling, instructions-for-use, and sterilization, as approved by BioForm. BioForm will develop and implement packaging and labeling for Company Product, subject to applicable regulatory requirements and consent of Supplier, which consent shall not be unreasonably withheld or delayed, to clearly differentiate Company Product from BioGlue Surgical Adhesive products sold by Supplier. Supplier shall ensure that all Company Product shall be labeled in accordance with the procedures specified from time to time by BioForm and BioForm shall have final approval over all packaging and labeling for Company Product, except for the consent provided for in the immediately preceding sentence. BioForm maintains the right to over-label Company Product as it deems necessary, but shall not utilize Supplier Trademarks except in accordance with Section 7.1, and shall provide Supplier with copies of any additional labels used by BioForm. **** Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.
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Product Specifications; Packaging and Labeling. All Products sold by JV hereunder shall be in full compliance with the Product Specifications established by Medifocus and approved by the Regulatory Authorities in the Territory, and shall be ready for use and operation by the end-user, including all packaging, labeling, instructions-for-use and sterilization as approved by Medifocus. Subject to all applicable Regulatory Authority requirements, all Products shall be labeled (including bar coding/UPN numbers) in accordance with the procedures specified from time to time by Medifocus, and Medifocus shall have final approval over all packaging and labeling for Products and all reasonable costs of implementing all requests for changes (regardless of reason) to the packaging and labeling of the Products shall be borne by JV. JV maintains the right to overlabel Products as it deems necessary but shall not utilize Trademarks except in accordance with Article V, and shall provide Medifocus with copies of any additional labels used by JV. If either party becomes aware of any information about any Product indicating that it may not conform to the Product Specifications then in effect, or that there are potential adulteration, misbranding and/or other issues regarding safety or effectiveness, it shall promptly notify the other party. The parties shall discuss in good faith the appropriate course of action, including recall of the Product in accordance with the provisions of Section 4.04, if necessary.
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Product Specifications; Packaging and Labeling. All products delivered by Novadaq hereunder shall be in compliance with Product Specifications and shall be ready for end-user sale, including all packaging, labeling, instructions-for-use and sterilization.
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Product Specifications; Packaging and Labeling. All Company Products delivered by AMS hereunder shall be in full compliance with the Product Specifications for such Company Product and shall be ready for end-user sale, including all packaging, labeling, instructions-for-use and sterilization required by the applicable Product Approval and as agreed by BSC and AMS. BSC shall have final approval over all labeling for Company Products to be distributed by BSC under this Agreement which approval shall not be unreasonably withheld. AMS shall consult with BSC with respect to the package of the Company Products to be distributed by BSC under this Agreement and any proposed modifications thereof. AMS acknowledges and agrees that all AMS-Developed Products shall be packaged and labeled in a manner, and shall have a cosmetic appearance and a specifically encoded smart-chip, that differentiates such AMS-Developed Product from (i) all comparable products, including Company Products, sold outside the Field and, (ii) as agreed by AMS and BSC, all comparable products, including Company Products, sold in other Specialties within the Field. AMS shall include trademarks and tradenames of BSC in the packaging and labeling of all Company Products as reasonably requested by BSC. BSC shall have the right to sell the Company Products as BSC private label products.
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Product Specifications; Packaging and Labeling. All BIS-Screen Products delivered by a Manufacturer hereunder shall be in full compliance with the Product Specifications for such BIS-Screen Product and shall be ready for end-user sale, including all packaging, labeling, instructions-for-use and sterilization required by the applicable Product Approval and as agreed by BSC and AMS. BSC shall have final approval over all labeling for BIS-Screen Products to be distributed by BSC under this Agreement which approval shall not be unreasonably withheld. AMS shall consult with BSC with respect to the package of any BIS-Screen Products manufactured by AMS and distributed by BSC under this Agreement and any proposed modifications thereof. AMS shall include trademarks and tradenames of BSC in the packaging and labeling of all BIS-Screen Products manufactured by AMS for distribution by BSC as reasonably requested by BSC. BSC shall have the right to sell any such BIS-Screen Products as BSC private label products.
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Product Specifications; Packaging and Labeling. All Products delivered by Supplier hereunder shall be in full compliance with the Product Specifications and shall be ready for end-user sale, including all packaging, labeling, instructions-for-use and sterilization as approved by BSC and Supplier. All Products shall be labeled (including bar coding/UPN numbers) in accordance with procedures mutually agreed upon by the parties. Subject to Section 4.6 below, BSC may, at its option, include any Product as a component in any kit or collection of products. In no event may BSC overlabel the Products or make changes to the labeling, instructions for use, or packaging without the prior approval of Supplier.
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Product Specifications; Packaging and Labeling. All QSTM Private Label Products manufactured and delivered by IMX hereunder shall be in full compliance with Product Specifications and shall be ready for end-user sale, including all packaging, labeling, and instructions for use as approved by Rapiscan. All QSTM Private Label Products shall include the Rapiscan brand names. The design, size and location of each of such brand name shall be determined by Rapiscan in its sole discretion, and be labeled (including without limitation bar coding/UPN numbers) in accordance with the procedures specified from time to time by Rapiscan and Rapiscan shall have the right to review and comment on all packaging and labeling for the QSTM Private Label Products sold to Rapiscan on a private label basis. Rapiscan may, in its sole option, include any QSTM Private Label Products as a component in any kit or collection of other products sold by Rapiscan into the Security Market.
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Product Specifications; Packaging and Labeling. All Products delivered by Celsion hereunder shall be in full compliance with the Product Specifications and shall be ready for use and operation by the end-user, including all packaging, labeling, instructions-for-use and sterilization as approved by BSC. Subject to all applicable Regulatory Authority requirements, all Products shall be labeled (including bar coding/UPN numbers) in accordance with the procedures specified from time to time by BSC, and BSC shall have final approval over all packaging and labeling for Products; provided, however, that the reasonable cost of implementing all requests for changes (other than changes required by Law) to the packaging and labeling of the Products subsequent to BSC's initial requests with respect to the packaging and labeling of the Products shall be borne by BSC. BSC maintains the right to overlabel Products as it deems necessary but shall not utilize Trademarks except in accordance with Article V, and shall provide Celsion with copies of any additional labels used by BSC. BSC may, at its option, include any Product as a component in any kit or collection of products (a "Bundled Product").
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Related to Product Specifications; Packaging and Labeling

  • Product Specifications The Company agrees that all Products sold to Xxxx hereunder shall conform to the respective specifications set forth on Schedule A or to such other specifications as are from time to time agreed upon by the Parties.

  • 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.

  • 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.

  • 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.

  • Technical Specifications The Technical Specifications furnished on the CD are intended to establish the standards for quality, performance and technical requirements for all labor, workmanship, material, methods and equipment necessary to complete the Work. When specifications and drawings are provided or referenced by the County, these are to be considered part of the Scope of Work, and to be specifically documented in the Detailed Scope of Work. For convenience, the County supplied specifications, if any, and the Technical Specifications furnished on the CD.

  • Labeling and Packaging Seller shall label and package Products in accordance with applicable Legal Requirements and Specifications and shall include a unique identifying lot number.

  • Quality Agreement Concurrently with execution of this Agreement, the Parties will enter into an agreement that details the quality assurance obligations of each Party with respect to the Manufacture and supply of Supplied Products under this Agreement (the “Quality Agreement”). Each Party shall perform its obligations under the Quality Agreement in accordance with the terms and conditions thereof. In the event of a conflict between the terms of the Quality Agreement and the terms of this Agreement, the provisions of the Quality Agreement shall govern.

  • Specifications That part of the Contract Documents consisting of written requirements for materials, equipment, systems, standards, and workmanship as applied to the Work, and certain administrative requirements and procedural matters applicable thereto. The term "Specifications" shall also include all written matter in the Project Manual or on the drawings and any Addenda or Change Orders thereto.

  • 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.

  • 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.

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