Food and Drug Laws definition

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

• 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.

• This Section 4.07 does not relate to compliance with Laws or Governmental Authorizations to the extent relating to Tax matters, which are the subject of Section 4.08, Intellectual Property matters, which are the subject of Section 4.09, or compliance with (i) the rules or regulations of the FDA or any comparable Healthcare Regulatory Authority having jurisdiction over the Asset Seller Entities or (ii) matters the subject of Food and Drug Laws and Health Care Laws, which are the subject of Section 4.12.

• Exhibitors must comply with all laws and regulations applicable to their Exhibit Booth, their activities related to their exhibit booth, meeting attendees, or their involvement in the Event, including but not limited to the Americans with Disabilities Act, Food and Drug Laws, and Privacy Laws.

• Comply with requirements of all applicable laws, rules, regulations and orders of any Governmental Authority (including all Pure Food and Drug Laws), except to the extent that failure to comply herewith could not, in the aggregate, have a Material Adverse Effect (other than any non-compliance solely with respect to the ABA Pension Plan).

• No more than two club athletes may participate for the same team in their respective or alike intramural sport, activity or event.

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 has the meaning ascribed thereto in in Section (23)(c) of Schedule “E”.

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 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 federal, state or local statues, rules, regulations, ordinances and codes, together with all administrative orders, directed duties, licenses, authorization and permits of, and agreements with, any United States and foreign Governmental Authority, in each case relating to manufacture, sale, testing, handling, management, marketing and disposal or pharmaceutical, medical device, biological and drug products, including but not limited to those relating to good manufacturing practices, good clinical practices, labeling, record keeping and obligations for products for which (a) monograph conditions must be met, or (b) a 510K or similar application must be filed, or (c) approval of the FDA and/or similar foreign Governmental Authority is required, before they may be marketed or sold.