LABELING OF PRODUCTS Sample Clauses

LABELING OF PRODUCTS. PLC shall and PLC Parent shall cause PLC to provide and to assume regulatory responsibility for all finished Product and Product-related labeling, including regulatory responsibility for all sales and marketing literature prepared by Novadaq, such that it complies with all applicable laws and regulations in the Territory during the term of this Agreement. All labeling for the Products shall include the statement “Distributed by Novadaq Corp., Manufactured by PLC Medical Systems, Inc.”
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LABELING OF PRODUCTS. Within one (1) year following the Closing Date, Purchaser shall remove to the extent practicable the name "OrthoLogic," "OrthoLogic Canada" or any similar name from Products, packaging materials, or promotional materials that exist as of the Closing Date. Purchaser shall be deemed to have a license to use such names on such Products and materials during such period of time. Nothing contained herein shall exclude Purchaser from using the name "OrthoRehab" or "OrthoRehab, Inc." on such Products or materials or otherwise in its business. Such name is being transferred to Purchaser pursuant to Section 1.2(k) hereof.
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LABELING OF PRODUCTS. This Agreement applies to PRL Motorsports Products. Unless otherwise agreed by PRL Motorsports in a separate agreement, Dealer shall use PRL Motorsports’s specified trademark only for purposes of advertisement, promotion, and sale of the corresponding Products and for no other purposes. Dealer shall use such trademark in accordance with the guidelines established by PRL Motorsports from time to time. Dealer shall not use any of PRL Motorsports's trademarks, service marks, logos, or slogans in any manner likely to confuse, mislead, or deceive the public, or to be adverse to the best interests of PRL Motorsports.
Sample 1
LABELING OF PRODUCTS. Guidant shall have the right to label the Products distributed under this Agreement; provided, however, that Guidant agrees to credit Thoratec as the manufacturer, and to include the Thoralon(TM) biomaterial brand name, on the Product packaging, brochures, advertisements and any other promotional materials or devices; and provided further that Guidant may use either Thoratec's Vectra(TM) vascular access graft mark xx Guidant's own mark xx identify the Products. If Guidant uses its own mark xx identify the Products, Guidant agrees that, upon termination of this Agreement, it will assign to Thoratec its rights in such mark xxx no additional consideration. Both parties agree that the labeling of the Products shall be in accordance with applicable regulations in the Territory. Guidant shall provide to Thoratec a sample of Product packaging, brochures, advertising and other promotional materials that include the Vectra(TM) mark xx that contain technical information regarding the Products for review and approval prior to Guidant's commercial use of such materials. If Thoratec has not provided Guidant with written notice of its disapproval and request for correction within ten (10) days of receipt of such materials, Thoratec shall be deemed to have approved such materials.
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LABELING OF PRODUCTS. 6 SECTION 4.4. Clinical or Marketing Studies...................................................6 SECTION 4.5. Installation Services and Services Provided under Extended Service Agreements...6
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LABELING OF PRODUCTS. 6.1 STERION shall label and individually package the Products in such a manner that the Products are ready for market and delivery to the Customer, unless otherwise directed by STERIS. For each individual Product package, STERION shall provide label instructions for use in all countries as directed by STERIS. STERION shall be responsible for ensuring that the Products are labeled, and include product label instructions, in accordance with all applicable laws, regulations and registrations. STERION shall label the Products with the STERIS trademark and logo (the “STERIS Xxxx”), such other brand names and logos as are specified by STERIS (the “Other Marks”) and, for a period of no more than six months from the Effective Date, the STERION trademark and logo (the “STERION Xxxx”) in accordance with the terms and conditions of the Purchase Agreement, in the manner directed by STERIS. Except for the STERIS Xxxx, the Other Marks and the STERION Xxxx, no other brand name, trademark or logo shall be affixed to the labeling or packaging of the Products.
Sample 1
LABELING OF PRODUCTS. Products sold to Customers by Abbott hereunder shall be labeled as manufactured by ICU and shall be marked with an Abbott list number and lot number pursuant to Section 8.5. All Product packaging shall be of the type normally and customarily used by ICU in its production process, and shall support the label claim(s).
Sample 1
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LABELING OF PRODUCTS. Guidant shall have the right to label the Products distributed under this Agreement in order to add its name and trademark, and in accordance with applicable regulations.
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LABELING OF PRODUCTS. EPD shall place Sionix data plate, labels, logos and artwork supplied by Sionix on the Private Label Products and on associated manuals, blueprints and specification sheets, in the size, format and location specified by Sionix (the "Sionix Marks"). Sionix hereby grants EPD a limited license to utilize and reproduce the Sionix Labels for the Private Label Products manufactured under this Agreement. EPD shall not use the Sionix Marks for any other purpose, without the prior written consent of Sionix. Upon expiration or termination of this Agreement, the foregoing limited license shall automatically be terminated without further action by either party hereto.
Sample 1

Related to LABELING OF PRODUCTS

  • Marking of Licensed Products To the extent commercially feasible and consistent with prevailing business practices, Company shall xxxx, and shall cause its Affiliates and Sublicensees to xxxx, all Licensed Products that are manufactured or sold under this Agreement with the number of each issued patent under the Patent Rights that applies to such Licensed Product.

  • 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.

  • 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.

  • 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.

  • 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.

  • 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.

  • Licensed Products Lessee will obtain no title to Licensed Products which will at all times remain the property of the owner of the Licensed Products. A license from the owner may be required and it is Lessee's responsibility to obtain any required license before the use of the Licensed Products. Lessee agrees to treat the Licensed Products as confidential information of the owner, to observe all copyright restrictions, and not to reproduce or sell the Licensed Products.

  • Supply of Materials The following materials will be supplied by the department Name of Materials Rate. Place of delivery 1.

  • 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.

  • Sale of Products 11.1. All Products sold to the Customer shall remain the property of Proximus until they have been paid for in full, including all charges and taxes. In case of a deterioration of the Product, the unpaid part of the sales price shall become due immediately. For as long as the Customer has not paid the Product's sales price in full, the provisions relating to product rental shall apply.

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