Food and Drug Laws means all applicable laws and regulations in the United States and Canada relating to the development, testing, manufacturing and distribution of pharmaceutical products. Except as set forth in the Current SEC Documents or such that do not cause a Material Adverse Effect, the Company has all necessary governmental approvals required under all Food and Drug and Environmental Laws and used in its business or in the business of any of its subsidiaries.
Food and Drug Laws means, collectively, (i) the Federal Food, Drug and Cosmetic Act, 21 U.S.C. 301 et seq., as amended from time to time, together with any rules and regulations promulgated thereunder, and any similar law, and analogous foreign or state laws and their respective implementing regulations, to the extent that such laws, rules or regulations regulate Food Products and/or Drugs, and (ii) any other applicable federal, state and municipal, domestic and foreign law governing the safety, purity, labeling, distribution, and advertising of Food Products and/or Drugs sold for consumption from time to time; and, in respect of all such laws, all rules, regulations and orders administered by the U.S. Food and Drug Administration or any other Governmental Entity, in each case, which impose standards with respect to the safety and marketing of Food Products and/or Drugs, including any such laws relating to the manufacture, labeling, packaging, transportation, distribution or sale of such products.
Food and Drug Laws means any applicable laws, rules, regulations, ordinances and administrative manuals, orders, guidelines, guidances and requirements issued by any Governmental Authority relating to the compounding, development, design, premarket clearance, approval, collection, manufacture, processing, holding, storing, testing, labeling, packaging, repackaging, packing, transporting, shipping, importing, exporting, marketing, advertising, promotion, sale, installation, servicing, and distribution of food, drugs, biological products, cosmetics and/or medical devices including components and accessories including, without limitation, the Federal Food Drug, and Cosmetic Act, 21 U.S.C. § 321 et seq., and all analogous federal, state, local, municipal, foreign, multinational, foreign regional, and foreign national laws, rules, orders, binding agreements, regulations, statutes, directives, standards, ordinances, codes or requirements of any Governmental Authority.
Examples of Food and Drug Laws in a sentence
This action arises under the Patent Laws of the United States and the Food and Drug Laws of the United States, Titles 35 and 21, United States Code.
Company shall, and shall cause each of its Subsidiaries to, comply with the requirements of all applicable laws, rules, regulations and orders of any governmental authority (including all Pure Food and Drug Laws), noncompliance with which could reasonably be expected to cause a Material Adverse Effect.
Warranty claims of the Customer shall be excluded in the case of negligible deviation of the agreed appearance and workmanship or if the use of the product is only impaired in a more than slight manner.
Update (Published by Food and Drug Laws Institute) 6: (November/December): 22-24, 2005.
Notwithstanding anything contained in this Section 5.10, no representation or warranty shall be deemed to be made in this Section 5.10 in respect of compliance with ERISA, the Foreign Corrupt Practices Act, Environmental Laws, Food and Drug Laws, Health Care Laws or Applicable Laws governing Taxes, employee benefits or the employment of labor, which are contained in other Sections of this Agreement.
More Definitions of Food and Drug Laws
Food and Drug Laws means the United States Federal Food, Drug, and Cosmetic Act of 1938, as amended (21 U.S.C. §§ 301 et seq.) and similar or related Laws relating to medical devices or components of medical devices.
Food and Drug Laws means the applicable provisions and requirements of the Federal Food, Drug and Cosmetic Act, as amended, 21 USC ss.301 ET SEq., and ss.355 ET Seq., and the rules and regulations promulgated thereunder, as well as all state and local laws, regulations, rules and ordinances relating thereto.
Food and Drug Laws means the United States Federal Food, Drug, and Cosmetic Act of 1938, as amended (21 U.S.C. §§ 301 et seq.), and similar domestic, foreign or related Laws relating to medical devices or components of medical devices.
Food and Drug Laws means all Laws applicable to the Company and its business, including those enforced by the DEA and FDA.
Food and Drug Laws has the meaning ascribed thereto in in Section (23)(c) of Schedule “E”.
Food and Drug Laws means the all Applicable Laws governing the development, testing, manufacturing, marketing, sale storage, transport or distribution of Xxxxxx’x products, medical devices or components of medical devices.
Food and Drug Laws means all applicable laws and regulations in the United States and Canada relating to the development, testing, manufacturing and distribution of pharmaceutical products. Except as set forth in the Form 20-F or on Schedule 3.1(s) hereto, the Company has all necessary governmental approvals required under all Food and Drug and Environmental Laws and used in its business or in the business of any of its subsidiaries. The Company and each of its subsidiaries are also in compliance with all other limitations, restrictions, conditions, standards, requirements, schedules and timetables required or imposed under all Food and Drug and Environmental Laws. Except for such instances as would not individually or in the aggregate have a Material Adverse Effect, there are no past or present events, conditions, circumstances, incidents, actions or omissions relating to or in any way affecting the Company or its subsidiaries that violate or would violate any Food and Drug or Environmental Law after the Closing or that may give rise to any liability, or otherwise form the basis of any claim, action, demand, suit, proceeding, hearing, study or investigation under any Environmental Law or Food and Drug Law.