Buyer Labeling definition

Buyer Labeling means the printed labels, labeling and packaging materials, including printed carton, container label and package inserts, used by Buyer and bearing Buyer's name for each Product.
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Buyer Labeling means the printed labels, labeling and packaging -------------- materials, including printed carton, container label and package inserts, used by Buyer and bearing Buyer's name for the Product.
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Buyer Labeling means trade dress, the printed labels, labeling and packaging materials, including mock-ups, printed cartons, carton and container labels and package inserts, used by Buyer and bearing Buyer’s name, logo or NDC number for, or in connection with, the packaging and labeling of the Products.
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Examples of Buyer Labeling in a sentence

  • Following Closing, Buyer shall at its own expense and as expeditiously as possible use all reasonable efforts to notify FDA of the transfer and to obtain such FDA approvals necessary for Buyer Labeling for each Product.

  • Following the Closing, Buyer shall at its own expense and as expeditiously as possible use all reasonable efforts to obtain such FDA approvals necessary for Buyer Labeling for the Product to be manufactured after the Closing.

  • In accordance with Section 7.1, Buyer is responsible for having Buyer Labeling submitted to the FDA as soon as possible following Closing.

  • In accordance with Section 7.2, Buyer is responsible for having the Buyer Labeling approved by the FDA as soon as possible.

  • In accordance with Section 7.2, Buyer is responsible for having the Buyer Labeling approved by the HPB as soon as possible.

  • Following Closing, Buyer shall at its own expense and as expeditiously as possible use all reasonable efforts to obtain such HPB approvals necessary for the Buyer Labeling for each Product.

  • Following the Closing, Buyers shall at their own expense and as expeditiously as possible use commercially reasonable efforts to obtain such FDA approvals necessary for Buyer Labeling for the Product to be manufactured after the Closing.

  • No changes made on this rider shall be valid unless countersigned by Artist.

  • Following the Closing, Buyer shall at its own expense and as expeditiously as possible use all reasonable efforts to obtain Buyer Labeling for the Product to be manufactured after the Closing.

  • Following the Closing, Buyer shall, at its own expense and as expeditiously as possible, use all reasonable efforts to obtain such FDA approvals necessary for Buyer Labeling for the Products to be manufactured after the Closing and, promptly comply with such FDA approvals upon receipt thereof.


More Definitions of Buyer Labeling

Buyer Labeling means the printed labels, labeling and packaging materials, including printed carton, container labels and package inserts, used by Buyer and bearing Buyer's name for, or in connection with, packaging of Infergen.
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Buyer Labeling means the printed labels, labeling and packaging materials, including printed carton, container labels and package inserts, used by Buyers or their Affiliates ***Certain information on this page has been omitted and filed separately with the Commission. Confidential treatment has been requested with respect to the omitted portions. and bearing the name of a Buyer (or any of their Affiliates) for the Product.
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Related to Buyer Labeling

  • Product Labeling means, with respect to a Licensed Product in a country or other jurisdiction in the Territory, (a) the Regulatory Authority-approved full prescribing information for such Licensed Product for such country or other jurisdiction, including any required patient information, and (b) all labels and other written, printed, or graphic matter upon a container, wrapper, or any package insert utilized with or for such Licensed Product in such country or other jurisdiction.

  • Labeling means all labels and other written, printed, or graphic matter on an article or any of its

  • Promotional Material means any communication that relates to the Company or its services made to or directed at, or that relates in any way to the solicitation of a Prospective Customer or a transaction in an Existing Customer’s trading account. Promotional Material includes, but is not limited to, published written texts, training materials, advertisements, market analysis, research reports, correspondence to Existing Customers or Prospective Customers, newsletters and generally anything written that assists in the solicitation process.

  • Promotional Materials means all sales representative training materials and all written, printed, graphic, electronic, audio or video matter, including, without limitation, journal advertisements, sales visual aids, formulary binders, reprints, direct mail, direct-to-consumer advertising, internet postings and sites and broadcast advertisements intended for use or used by either Party or its Affiliates or sublicensees in connection with any promotion of a Product.

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

  • Spray buff product means a product designed to restore a worn floor finish in conjunction with a floor buffing machine and special pad.

  • API means the American Petroleum Institute.

  • Finished Products means the fully assembled and shrink-wrapped Licensed Products, each including a Game Cartridge, Game Cartridge label and Printed Materials.

  • Drug Product means a specific drug in dosage form from a known source of manufacture, whether

  • Manufacturing Materials means parts, tools, dies, jigs, fixtures, plans, drawings, and information produced or acquired, or rights acquired, specifically to fulfill obligations set forth herein.

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

  • Product Specifications means those Manufacturing, performance, quality - control release, and Fill/Finish specifications for Drug Substance or Licensed Product in the Territory, which are initially as set forth in the applicable Regulatory Approval for a Licensed Product, as such specifications may be amended from time to time pursuant to the terms of this Agreement.

  • Edible cannabis product means cannabis product that is intended to be used, in whole or in part, for human consumption, including, but not limited to, chewing gum, but excluding products set forth in Division 15 (commencing with Section 32501) of the Food and Agricultural Code. An edible cannabis product is not considered food, as defined by Section 109935 of the Health and Safety Code, or a drug, as defined by Section 109925 of the Health and Safety Code.

  • MSAA Indicator Technical Specifications document means, as the context requires, either or both of the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Indicator Technical Specifications November 5, 2018 Version 1.3” and the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Target and Corridor-Setting Guidelines” as they may be amended or replaced from time to time;

  • labelling means any words, particulars, trade marks, brand name, pictorial matter or symbol relating to a food and placed on any packaging, document, notice, label, ring or collar accompanying or referring to such food;

  • Drug outlet means a pharmacy, nursing home, shelter home, convalescent home, extended care facility, drug abuse treatment center, penal institution, hospital, family planning clinic, student health center, retail store, wholesaler, manufacturer, mail-order vendor or other establishment with facilities located within or out of this state that is engaged in dispensing, delivery or distribution of drugs within this state.

  • Bulk drug substance means any substance that is represented for use, and that, when used in the

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • Vapor product means any:

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

  • complex product means a product which is composed of multiple components which can be replaced permitting disassembly and re-assembly of the product.

  • Packaging Materials means art and mechanical formats for a Software Title including the retail packaging, end user instruction manual with end user license agreement and warranties, end user warnings, FPU media label, and any promotional inserts and other materials that are to be included in the retail packaging.

  • Manufacturing site means the facilities where a Compound is Manufactured by or on behalf of a Party, as such Manufacturing Site may change from time to time in accordance with Section 8.7.

  • Anti-Static Product means a product that is labeled to eliminate, prevent, or inhibit the accumulation of static electricity. “Anti-Static Product” does not include “Electronic Cleaner,” “Floor Polish or Wax,” “Floor Coating,” and products that meet the definition of “Aerosol Coating Product” or “Architectural Coating.”

  • Product Manufacturer means the entity that assembles the component parts to manufacture the final Product;