Marketing Laws definition

Marketing Laws means the Telephone Consumer Protection Act, the Controlling the Assault of Non-Solicited Pornography and Marketing (CAN-SPAM) Act, the Telemarketing Sales Rule, and any other applicable laws of similar effect relating to commercial email, text messages and other types of messages.
Marketing Laws means, to the extent applicable to Seller or any of its Affiliates, all Applicable Laws pertaining to direct marketing, e-mails, text messages, telemarketing and telephone calls, and the sending of solicited and unsolicited electronic marketing communications, including the CAN-SPAM Act, the Telephone Consumer Protection Act, and the Telemarketing Sales Rule.
Marketing Laws means all Laws with respect to advertising and marketing, including the Telephone Consumer Protection Act (47 U.S.C. § 227), CAN-SPAM (15 U.S.C. §7701), the Telemarketing Sales Rule (16 C.F.R. Part 310), state and federal laws addressing unfair and deceptive trade practices, the Federal Trade Commission’s Enforcement Policy Statement on Deceptively Formatted Advertising (81 Fed. Reg. 22596), the Federal Trade Commission’s Guides Concerning Use of Endorsements and Testimonials in Advertising (16 C.F.R. 255.5), CA Business & Professions Code § 17529, Canada’s Anti-Spam Law (CASL), and the similar Laws of any other jurisdiction.

Examples of Marketing Laws in a sentence

  • Each of the Company and its Subsidiaries are, and since January 1, 2019 have been, in compliance in all material respects with all applicable Laws, including the applicable Marketing Laws.

  • Neither the Company nor any of its Subsidiaries has, since January 1, 2008, as of the date of shipment, released products that are “adulterated,” “misbranded,” “contaminated,” or “mislabeled” in any material respect within the meaning of any applicable Food Safety and Marketing Laws, or otherwise unfit for human consumption under any applicable Food Safety and Marketing Laws.

  • Certification of Storage Premises1 All storage warehouses shall be inspected for their suitability by the Director- General of LACRA, or an officer acting on his behalf and a certificate of registration shall be issued if conditions are ideal and in accordance with the Produce Marketing Laws of Liberia, 1974 or other relevant or applicable regulations/guidelines.

  • There is no charge, claim, assertion or action against the Company or any of its Subsidiaries, or any pending investigations by any Governmental Entity, of the Company or any of its Subsidiaries relating to Marketing Laws.

  • CMG will not be responsible for any failure of the Pass to comply with applicable laws (including applicable Marketing Laws), or any violations of Advertiser’s end- user terms of use, nor will it be responsible for any Advertiser Content included on Advertiser’s Pass.

  • According to Christensen (2014) stated “Ethics is an important part of marketing and the Marketing Laws, but since the perspective may differ depending on society, situations and culture, it is necessary to understand what ethics is and how it is used in the society.” While explaining moral foundation of ethical research, Price et al.

  • State Pharmaceutical and Medical Device Marketing Laws If not preempted by the PPACA, several jurisdictions require pharmaceutical companies to report expenses related to the marketing and promotion of pharmaceutical products and to report gifts and payments to healthcare practitioners in those jurisdictions, or to obtain licenses for sales representatives and require them to satisfy educational and other requirements.


More Definitions of Marketing Laws

Marketing Laws means all Legal Requirements applicable to advertising, e-mails, text messages, telemarketing and direct marketing, including the Telephone Consumer Protection Act (47 U.S.C. § 227), CAN-SPAM (15 U.S.C. §7701), the Telemarketing Sales Rule (16 C.F.R. Part 310), state and federal laws addressing unfair and deceptive trade practices, state consumer protection Legal Requirements, the Federal Trade Commission Act, the Federal Trade Commission’s Enforcement Policy Statement on Deceptively Formatted Advertising (81 Fed. Reg. 22596), the Federal Trade Commission’s Guides Concerning Use of Endorsements and Testimonials in Advertising (16 C.F.R. 255.5), the Federal Trade Commission’s Native Advertising Guidelines, CA Business & Professions Code § 17529, and the similar Legal Requirements of any other jurisdiction, all the foregoing to the extent applicable to the Company.
Marketing Laws has the meaning set forth in Section 4.27(a).

Related to Marketing Laws

  • Medical marijuana product means a product that contains cannabinoids that have been extracted from plant material or the resin therefrom by physical or chemical means and is intended for administration to a licensed patient, including but not limited to concentrates, oils, tinctures, edibles, pills, topical forms, gels, creams, and other derivative forms, except that this term does not include live plant forms.

  • Commercialization or “Commercialize” means activities directed to marketing, promoting, research and development as required, manufacturing for sale, offering for sale, distributing, importing or selling a product, including sub-licensing or sub-contracting of these activities.

  • Territory means worldwide.

  • Marijuana products means concentrated marijuana products and marijuana products that are comprised of marijuana and other ingredients and are intended for use or consumption, such as, but not limited to, edible products, ointments, and tinctures.

  • 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.

  • 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.

  • Investigational Product means the Study Drug identified above and the control material, as further detailed in the Protocol;

  • Marijuana product means marijuana as defined in 50-32-101 and marijuana-infused products

  • WTO GPA country end product means an article that—

  • Cannabis products means cannabis that has undergone a process whereby the plant material has been transformed into a concentrate, including, but not limited to, concentrated cannabis, or an edible or topical product containing cannabis or concentrated cannabis and other ingredients.

  • Union territory means the territory of—

  • Regulatory Materials means regulatory applications, submissions, notifications, registrations, Marketing Authorizations or other written materials, correspondence, submissions made to or with a Regulatory Authority that are necessary or reasonably desirable in order to Develop, Manufacture or Commercialize the Licensed Products in the Field in a particular country.

  • Manufacturing Know-How means all information, techniques, inventions, discoveries, improvements, practices, methods, knowledge, skill, experience and other technology, whether or not patentable or copyrightable, and any copyrights based thereon, relating to or necessary or useful for the production, purification, packaging, storage and transportation of Collaboration Products, including without limitation specifications, acceptance criteria, manufacturing batch records, standard operating procedures, engineering plans, installation, operation and process qualification protocols for equipment, validation records, master files submitted to the FDA, process validation reports, environmental monitoring processes, test data including pharmacological, toxicological and clinical test data, cost data and employee training materials.

  • Marihuana-infused product means a topical formulation, tincture, beverage, edible substance, or similar product containing marihuana and other ingredients and that is intended for human consumption.

  • Commercial or marketing purpose means the sale of student data; or its use or disclosure for purposes of receiving remuneration, whether directly or indirectly; the use of student data for advertising purposes, or to develop, improve, or market products or services to students.

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

  • Marketing Approval means all approvals, licenses, registrations or authorizations of the Regulatory Authority in a country, necessary for the manufacture, use, storage, import, marketing and sale of a Product in such country.

  • Commercializing means to engage in Commercialization and “Commercialized” has a corresponding meaning.

  • Manufacturing Technology means any and all patents, patent applications, know-how, and all intellectual property rights associated therewith that are owned or controlled by Licensor, and including all tangible embodiments thereof, that are necessary or useful for the manufacture of adeno-associated viruses, adeno-associated virus vectors, research or commercial reagents related thereto, Licensed Products, or other products, including manufacturing processes, technical information relating to the methods of manufacture, protocols, standard operating procedures, batch records, assays, formulations, quality control data, specifications, scale up, any and all improvements, modifications, and changes thereto, and any and all activities associated with such manufacture. Any and all chemistry, manufacturing, and controls (CMC), drug master files (DMFs), or similar materials provided to regulatory authorities and the information contained therein are deemed Manufacturing Technology.

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

  • Product Trademark means one or more trademarks or logos that are used for the Commercialization of a Product in the Field in the Territory.

  • FDA means the United States Food and Drug Administration and any successor agency thereto.

  • Hemp products means all products made from industrial hemp,

  • Product Trademarks means the Trademark(s) to be used by Adapt or its Affiliates or its or their respective Sublicensees for the Commercialization of Products and any registrations thereof or any pending applications relating thereto (excluding, in any event, any trademarks, service marks, names or logos that include any corporate name or logo of the Parties or their Affiliates).

  • 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.