Drug Laws means all Laws of any Jurisdiction relating to the manufacture, production, distribution, or development of drugs and drug products, including without limitation, the Federal Food, Drug and Cosmetic Act.
Drug Laws means the Food, Drug and Cosmetic Act, the Public Health Service Act, any Applicable Law promulgated by the EMA or similar laws of any foreign jurisdiction.
Drug Laws means the Federal Food, Drug, and Cosmetic Act, the Public Health Service Act, the United States anti-kickback statute, or the regulations and regulatory guidance promulgated thereunder or similar Legal Requirements of any foreign jurisdiction, including those relating to good laboratory practices, good clinical practices, adverse event reporting, good manufacturing practices, advertising and promotion, recordkeeping, and filing of reports.
Examples of Drug Laws in a sentence
Federal Drug Laws The possession, use, or distribution of illicit drugs is prohibited by federal law.
Wisconsin Illicit Drug Laws, the Uniform Controlled Substances Act, Wis.
The Commission recommends that ONDCP work with the DOJ, DOL, the National Alliance for Model State Drug Laws, the National Conference of State Legislatures, and other stakeholders to develop model state legislation/regulation for states to decouple felony convictions and eligibility for business/occupational licenses, where appropriate.
Categories of drugs include narcotics, barbiturates, stimulants, and hallucinogens (not to be confused with classes of drugs according to Commonwealth of Massachusetts Drug Laws).
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.
More Definitions of Drug Laws
Drug Laws means any Law related to the business of processing, manufacturing, labeling, distributing and selling any drug or drug component, including, but not limited to active pharmaceutical ingredients, meant for human or animal use, and any rule, regulation, directive, order, guidance or decision promulgated or issued pursuant thereto and applicable to the Seller or any of its Subsidiaries. For the avoidance of doubt, Drug Laws shall include the FDCA and 21 C.F.R. Parts 210 and 211 promulgated thereunder and the Chemical Diversion and Trafficking Act and any regulations promulgated thereunder.
Drug Laws has the meaning ascribed to it in Section 5.11(p).
Drug Laws means statutes, laws, ordinances, rules, regulations and administrative policies enforced by the FDA and comparable foreign Governmental Entities.
Drug Laws means all applicable Laws related to the research, development, testing, manufacture, processing, handling, packaging, labeling, storage, advertising, promotion, marketing, sale or distribution of the Products, including: (a) the Federal Food, Drug and Cosmetic Act (21
Drug Laws means such requirements of United States Law applicable to the Business and relating to (a) standards and requirements of the Food Drug and Administration and the Federal Food, Drug, and Cosmetic Act (21 U.S.C. § 301 et seq.), as amended, and implementing regulations; (b) standards and requirements of the DEA and the Controlled Substances Act (21 U.S.C. § 801 et seq.), as amended, and implementing regulations; (c) the licensure and regulation of manufacturers of prescription drugs, over-the-counter drugs, and controlled substances; (d) the licensure and regulation of controlled substance analytical laboratories by a Governmental Entity; and (e) all equivalent or similar Laws in any jurisdiction applicable to Sellers.
Drug Laws means all applicable Laws related to the research, development, testing, manufacture, processing, handling, packaging, labeling, storage, advertising, promotion, marketing, sale or distribution of the Products, including: (a) the Federal Food, Drug and Cosmetic Act (21 U.S.C. § 301 et seq.); (b) the Federal Controlled Substances Act (21 U.S.C. § 801 et seq.); (c) the Controlled Substances Import and Export Act (21 U.S.C. § 951, et. seq.); (d) regulations in Title 21 of the U.S. Code of Federal Regulations, including FDA regulations relating to Good Manufacturing Practice Requirements, Good Clinical Practice Requirements and Good Laboratory Practice Requirements, and applicable Company standard operating procedures; (e) all terms and conditions of any Healthcare Regulatory Authorization; (f) the Prescription Drug Marketing Act of 1987 (21 U.S.C. § 353 et seq.); (g) any state board of pharmacy Law or analogous Law in any applicable foreign jurisdiction, and all Laws relating to the operation of pharmacies, the dispensing of prescription drugs, the administration of prescription drug formularies, utilization management and pharmacy benefits management; (h) Laws pertaining to the possession, distribution or use of controlled substances; (i) the Drug Supply Chain Security Act; (j) Laws pertaining to the distribution or transportation of the Products; (k) Laws related to importation or exportation of the Products or any of their components; (l) Laws pertaining to expanded access programs; (m) FDA requirements applicable to help seeking and other disease awareness communications; and (n) Laws related to the advertising, promotion and marketing of the Products.
Drug Laws means all laws, rules and regulations that are applicable to the research, manufacture, use, sale, registration and promotion of pharmaceutical products for human use in a Party’s portion of the Territory and that materially affect the Party’s performance under this Agreement, including the United States Federal Food, Drug, and Cosmetic Act, the Public Health Service Act, and all rules and regulations promulgated thereunder, and any similar laws, rules or regulations in any country in the Bayer Territory. [ * ] Confidential Treatment Requested