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Food and Drug Law definition

Food and Drug Lawmeans any law in any way relating to the manufacture, composition, labeling, advertising, safety, production, holding, storage, or distribution of food products, including but not limited to the Federal Food, Drug, and Cosmetic Act (21 U.S.C. § 301 et seq.), the Food Safety Modernization Act (21 U.S.C. Chapter 27), the Fair Packaging and Labeling Act (15 U.S.C. § 1451 et seq.), and the Federal Trade Commission Act (15 U.S.C. § 41 et seq.), as each has been amended and the regulations promulgated pursuant thereto and, in each case, the equivalent law, regulation or order by a Governmental Authority in any applicable non-U.S. jurisdiction. IF "1" = "1" "#4875-2924-7575v15" "" #4875-2924-7575v15 AMERICAS 120585256
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Food and Drug Lawmeans the Federal Food, Drug and Cosmetic Act of 1938, the Federal Trade Commission Act, the Fair Packaging and Labeling Act, the Consumer Products Safety Commissions Poison Prevention Act, the Safe Drinking Water and Toxic Enforcement Act of 1986 or �Proposition 65� and analogous non-U.S. Requirements of Law (including, for the avoidance of doubt, the Cosmetics Regulation (EC) No. 1223/2009 on cosmetic products and Commission Regulation (EU) No 655/2013 laying down common criteria for the justification of claims used in relation to cosmetic products, including any amendments thereto and all relevant guidance in the European Union).
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Food and Drug Lawmeans any Law, policy, regulation or procedure of the FDA or the FTC or other Governmental Authority relating to the production, manufacture, processing, labeling, promotion, sale, distribution, transportation, holding, safety or efficacy of the products of the Company and its Subsidiaries or their regulation, including the FFDC Act, the Poultry Products Inspection Act (21 U.S.C. § 451 et seq.); the Egg Products Inspection Act (21 U.S.C. § 1031 et seq.), and the regulations, policies, and compliance guidance issued or administered by the FDA and any agencies within the USDA, including the Food Safety and Inspection Service.
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Examples of Food and Drug Law in a sentence

  • Bodily injury" or "property damage" arising out of the use, sale, manufacture, delivery, transfer or possession by any person of a Controlled Substance as defined by the Federal Food and Drug Law at 21 U.S.C.A. Sections 811 and 812.

  • Hostile fire means one which becomes uncontrollable or breaks out from where it was intended to be.d. Loss arising out of the use, sale, manufacture, delivery, transfer or possession of a controlled substance(s) as defined by the Federal Food and Drug Law at 21 U.S.C.A. sections 811 and 812.

  • Bodily injury" or "property damage" arising out of the use, sale, manufacture, delivery, trans- fer or possession by any person of a Con- trolled Substance as defined by the Federal Food and Drug Law at 21 U.S.C.A. Sections 811 and 812.

  • Arising out of the use, sale, manufacture, delivery, transfer or possession by any person of a Controlled Substance(s) as defined by the Federal Food and Drug Law at 21 U.S.C.A. Sections 811 and 812.

  • Keynote Address at the 2018 Food and Drug Law Institute Annual Conference, Washington, DC (May 3, 2018) (Emphasis added).

  • Arising out of the use, sale, manufacture, de- livery, transfer or possession by any person of a Controlled Substance(s) as defined by the Federal Food and Drug Law at 21 U.S.C.A. Sections 811 and 812.

  • Arising out of the use, sale, manufacture, deliv- ery, transfer or possession by any person of a Controlled Substance(s) as defined by the Federal Food and Drug Law at 21 U.S.C.A. Sections 811 and 812.

  • In 1986, a similar bill introduced into Congress140Hutt, Merrill, Food and Drug Law, Cases and Materials, Supra, note 63 at 35.‌�141Affidavit of Sam D.

  • Any person or company found to be in violation of any provision of the Food and Drug Law 1992, PNDCL 305B will be subject to a court penalty unit (the fine is not fixed) to be determined by the law court or imprisoned for not more two years or both.

  • Mossinghoff, Overview of the Hatch-Waxman Act and its impact on the drug development process, Food and Drug Law Journal, 54(2), 1999, p.


More Definitions of Food and Drug Law

Food and Drug Lawmeans any applicable U.S., foreign, federal, state or local law, statute, code, ordinance, rule, or regulation of the FDA or the FTC or other Governmental Authority relating to the manufacture, labeling, promotion, sale, safety or efficacy of the Products.
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Related to Food and Drug Law

  • Food and food ingredients means substances, whether in liquid, concentrated, solid, frozen, dried, or dehydrated form, that are sold for ingestion or chewing by humans and are consumed for their taste or nutritional value. Food and food ingredients do not include alcoholic beverages and tobacco.

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

  • New Drug Application or “NDA� means a New Drug Application filed with the FDA as described in 21 C.F.R. § 314, a Biological License Application (BLA) pursuant to 21 C.F.R. § 601.2, or any equivalent or any corresponding application for Regulatory Approval (not including pricing and reimbursement approval) in any country or regulatory jurisdiction other than the United States.

  • FFDCA means the United States Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 301 et seq., as amended from time to time, together with any rules, regulations and requirements promulgated thereunder (including all additions, supplements, extensions, and modifications thereto).

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