Marketing Rules definition

Marketing Rules is the defined term for the purposes of this Agreement to describe:
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Marketing Rules means the general marketing standard and the specific marketing standards covering fresh fruit and vegetables listed in Part IX of Annex I to Council Regulation 2013 and includes the rules relating to those standards contained in Articles 74, 75 and 76 of that Council Regulation and in Title II of Commission Implementing Regulation 543/2011;”,
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Marketing Rules means any of the minimum requirements, classification, sizing, presentation and marking standards provided for in Article 1 and Annex I of Commission Regulation 1333/2011, subject to the tolerances in Point IV of that Annex;”,
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Examples of Marketing Rules in a sentence

  • In compliance with the Marketing Rules for storage capacities, the Customer subscribes to a whole number of Storage Units, as defined in the Supplementary Conditions.

  • In addition to the general knowledge of the Communications Laws necessary to discharge his or her duties under this Consent Decree, the Compliance Officer shall have specific knowledge of the Equipment Marketing Rules prior to assuming his or her duties.

  • In addition to general knowledge of the Communications Laws necessary to discharge his/her duties under this Consent Decree, the Compliance Officer shall have specific knowledge of the Equipment Marketing Rules prior to assuming his/her duties.

  • In reference to article 4 “Specific Products” paragraph (b) of the Marketing Rules, the amount of the Guarantee is equal to the volume of Specific Product subscribed, valued at the future XXX xxxxx (“Season”) corresponding to the phase of injection of the Specific Product, published by the European Energy Exchange (“EEX”) on the day of the Specific Product auction.

  • The Applicant agrees to comply with the Marketing Rules for Green Star Projects as displayed on the Website in relation to its promotion of the Certified Rating in respect of a Project.

  • Any modification is brought to the attention of the Participants by the Storage Facility Manager at least five (5) days before the organization of the first auction governed by the modified Marketing Rules.

  • The GBCA grants to the Applicant for the duration of the Validity Period, a non-transferable, non-exclusive licence to use the Trade Mark showing the Designed Assessment or Certified Rating solely in relation to the Project and the display, promotion and advertisement of the Project, in accordance with the Marketing Rules.

  • The GBCA grants to the Applicant for the duration of the Validity Period, a non- transferable, non-exclusive licence to use the Trade Xxxx showing the Certified Rating solely in relation to the Project and the display, promotion and advertisement of the Project, in accordance with the Marketing Rules.

  • The Applicant will use the Trade Xxxx in accordance with the Marketing Rules and the Agreement.

  • The Applicant agrees to comply with the Marketing Rules for Green Star Projects as displayed on the Website in relation to its promotion of the Certified Rating or Designed Assessment in respect of a Project.


More Definitions of Marketing Rules

Marketing Rules has the meaning specified in Section 5.10(m).
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Related to Marketing Rules

  • Operating Rules means the operating rules of a CS Facility regulating the settlement, clearing and registration of uncertificated shares as amended, varied or waived (whether in respect of the Company or generally) from time to time which shall only apply to the Company during the Listed Period;

  • Marketing Plan has the meaning set forth in Section 4.3(a).

  • Regulatory Rules means all corporate and securities laws, regulations, rules, policies, notices, instruments and other orders of any kind whatsoever which may, from time to time, apply to the implementation, operation or amendment of this Plan or the Options granted from time to time hereunder including, without limitation, those of the applicable Regulatory Authorities.

  • Marketing program means a program established by order of the director pursuant to this act prescribing rules and regulations governing the marketing for processing, distributing, selling, or handling an agricultural commodity produced in this state or agricultural commodity input during a specified period and

  • AIM Rules means the rules published by the London Stock Exchange governing admission to AIM and the regulation of AIM companies as amended or re-issued from time to time;

  • Licensed clinical social worker means an individual who meets the licensed clinical social worker requirements established in KRS 335.100.

  • Trading Rules means the Rules and Regulations of the Exchange prescribed by the Stock Exchange from time to time; and

  • Listing Rules the Rules Governing the Listing of Securities on the Stock Exchange

  • Marketing Material means bank books, bank information memoranda, offering memoranda, offering circulars, road show presentations, prospectuses, registration statements and other information packages, similar materials and marketing materials (including, to the extent necessary, an additional bank information memorandum that does not include material non-public information), in each case, prepared in connection with the Financing and reasonably requested by Parent or the Financing Sources that is customarily delivered in connection with debt financings of the type being arranged.

  • ASX Listing Rules means the official listing rules of the ASX.

  • Clinical practice guidelines means a systematically developed statement to assist

  • WREGIS Operating Rules means those operating rules and requirements adopted by WREGIS as of December 2010, as subsequently amended, supplemented or replaced (in whole or in part) from time to time.

  • Good Clinical Practices means the FDA’s standards for the design, conduct, performance, monitoring, auditing, recording, analysis, and reporting of clinical trials contained in 21 C.F.R. Part 50, 54, 56, 312, 314, 320, 812, and 814 and (ii) “Good Laboratory Practices” means the FDA’s standards for conducting non-clinical laboratory studies contained in 21 C.F.R. Part 58.

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Commercialization Plan has the meaning set forth in Section 6.2.

  • Procurement Plan means the Recipient’s procurement plan for the Project, dated April 2, 2010, and referred to in paragraph 1.16 of the Procurement Guidelines and paragraph 1.24 of the Consultant Guidelines, as the same shall be updated from time to time in accordance with the provisions of said paragraphs.

  • Marketing Materials has the meaning ascribed thereto in NI 41-101;

  • Regulatory Authority means any federal, national, multinational, state, county, city, provincial, or local regulatory agency, department, bureau or other governmental entity with authority over the marketing, commercialization, manufacture or sale of a pharmaceutical product in the Territory, including the FDA in the United States and the EMA in the EU.

  • GEM Listing Rules the Rules Governing the Listing of Securities on GEM

  • Relevant Electric Retail Regulatory Authority means an entity that has jurisdiction over and establishes prices and policies for competition for providers of retail electric service to end- customers, such as the city council for a municipal utility, the governing board of a cooperative utility, the state public utility commission or any other such entity.

  • CFDA means the Code of Federal Domestic Assistance assigned to a federal grant.

  • Tobacco products means cigars, cigarettes, cheroots, stogies, periques, granulated, plug cut, crimp cut, ready rubbed, and other smoking tobacco, snuff, snuff flour, moist snuff, cavendish, ping and twist tobacco, fine-cut and other chewing tobaccos, shorts, refuse scraps, clippings, cuttings and sweepings of tobacco, and other kinds and forms of tobacco, prepared in such manner as to be suitable for chewing or smoking in a pipe or otherwise, or both for chewing and smoking.

  • Public Procurement Regulatory Authority (PPRA) means the Government Agency responsible for oversight of public procurement.

  • Pharmaceutical Product shall have the meaning ascribed to such term in Section 3.1(hh).

  • 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.

  • Regulatory Authorities means the Commissions and the Exchange;