Pharmaceutical Laws definition

Pharmaceutical Laws means federal, state and local laws, rules or regulations, codes, orders, decrees, judgments or injunctions issued, promulgated, approved or entered, relating to dispensing, storing or distributing prescription medicines or products, including laws, rules or regulations relating to the qualifications of Persons employed to do the same.
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Pharmaceutical Laws means, with respect to the United States, the United States Food, Drug and Cosmetic Act of 1938, as amended from time to time, and the regulations and guidelines promulgated thereunder, and with respect to any other governmental unit in the Territory (whether federal, state, municipal or other), the laws, regulations and guidelines of such governmental unit pertaining to pharmaceuticals, including the development, exportation, importation, use, manufacture, distribution, marketing and/or sale thereof.
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Pharmaceutical Laws has the meaning set forth in Section 3.7(b).
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Examples of Pharmaceutical Laws in a sentence

  • The Company and each Subsidiary has, in all material respects, complied with all laws, regulations and orders applicable to their respective businesses, including Pharmaceutical Laws (as defined below), and have all material permits and licenses required thereby.

  • Company employees with responsibilities in the areas governed by the FFDCA, FDA regulations and EU Pharmaceutical Laws are required to review, understand and comply with applicable laws and regulations.

  • This suggests that a more powerful means of support would therefore target such students with financial aid through bursaries, and more practical academic support throughout their time at university.

  • Pharmaceutical Laws means federal (including, without limitation, the FFDCA), state and local laws, rules or regulations, codes, orders, decrees, judgments or injunctions issued, promulgated, approved or entered, relating to dispensing, storing or distributing prescription medicines or products, including laws, rules or regulations relating to the qualifications of Persons employed to do the same.

  • Pharmaceutical Laws and Regulation are necessary because use of ineffective or poor quality drugs can result in therapeutic failure, worsening of disease condition, resistance development to drugs by microbes and even death resulting in undermining of the whole health sector.

  • Enact the necessary Pharmaceutical Laws and Regulations for the proper monitoring and control of the national pharmaceutical sector.

  • Cycle is committed to performing and conducting its business with integrity as demonstrated by compliance with federal, state, and other applicable laws, regulations, and guidance, including the Pharmaceutical Laws, Regulations, and Guidance discussed herein.

  • Adukiya, R., S., “Overview of Pharmaceutical Industry with Specific Reference to Pharmaceutical Laws of India”, PP., 1-97.

  • To Seller’s Knowledge, all preclinical and clinical investigations or trials sponsored by or conducted on behalf of Seller in connection with the Product have been conducted in material compliance with applicable Pharmaceutical Laws, including Good Clinical Practices requirements thereunder and Laws restricting the use and disclosure of individually identifiable health information.


More Definitions of Pharmaceutical Laws

Pharmaceutical Laws means Laws primarily regulating the testing, clinical trials, manufacturing, storage, packaging, sale or distribution of drugs and/or medical device products.
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Pharmaceutical Laws means the Pharmacy Act, 1991, the Drug and Pharmacies Regulation Act, 1990 the Regulated Health Professions Act, 1991 (each in force in the Province of Ontario from time to time) and the equivalent Laws or similar in other provinces or territories of Canada, the Controlled Drugs and Substances Act (Canada), the Food and Drugs Act (Canada), and the published rules, regulations, instruments and policies of any Governmental Authority administering those Laws, as well as all requirements, policies, directives, guidelines, guidance, principles, rulings, orders, decisions, interpretations, administrative views and codes and practices of any applicable Pharmaceutical Governing Body (whether in Ontario or otherwise) and the National Association of Pharmacy Regulatory Authorities and any applicable provincial or territorial pharmaceutical associations (whether in Ontario or otherwise).
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Pharmaceutical Laws means federal (including, without limitation, the FFDCA), state and local laws, rules or regulations, codes, orders, decrees, judgments or injunctions issued, promulgated, approved or entered, relating to dispensing, storing or distributing prescription medicines or products, including laws, rules or regulations relating to the qualifications of Persons employed to do the same. Plan – an employee benefit plan now or hereafter maintained for employees of any Loan Party or any of their Subsidiaries that is covered by Title IV of ERISA.
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Related to Pharmaceutical Laws

  • Radiopharmaceutical quality assurance means, but is not limited to, the performance of appropriate chemical, biological, and physical tests on potential radiopharmaceuticals and the interpretation of the resulting data to determine their suitability for use in humans and animals, including internal test assessment, authentication of product history, and the keeping of proper records.

  • Radiopharmaceutical means any drug that exhibits spontaneous disintegration of unstable nuclei with the emission of nuclear particles or photons and includes any non-radioactive reagent kit or radionuclide generator that is intended to be used in the preparation of any such substance, but does not include drugs such as carbon-containing compounds or potassium-containing salts that include trace quantities of naturally occurring radionuclides. The term also includes any biological product that is labeled with a radionuclide or intended solely to be labeled with a radionuclide.

  • Radiopharmaceutical service means, but is not limited to, the procurement, storage, handling preparation, labeling, quality assurance testing, dispensing, delivery, recordkeeping, and disposal of radiopharmaceuticals and other drugs.

  • Licensed health care practitioner means a physician, as defined in Section 1861(r)(1) of the Social Security Act, a registered professional nurse, licensed social worker or other individual who meets requirements prescribed by the Secretary of the Treasury.

  • Active Pharmaceutical Ingredient or “API” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

  • Pharmaceutical care means the provision of drug therapy and

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

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

  • Good Manufacturing Practices or “GMP” shall mean the then current Good Manufacturing Practices as such term is defined from time to time by the FDA or other relevant Governmental Authority having jurisdiction over the development, manufacture or sale of the Product in the Territory pursuant to its regulations, guidelines or otherwise.

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

  • FD&C Act means the United States Federal Food, Drug and Cosmetic Act, as may be amended from time to time.

  • Current Good Manufacturing Practices or “cGMP” means applicable Good Manufacturing Practices as specified in the United States Code of Federal Regulations and/or the EU Good Manufacturing Guidelines, and any successor legislation from time to time, prevailing at the time of the manufacture of the Product.

  • Medical marijuana means marijuana that is grown, processed, dispensed, tested, possessed, or used for a medical purpose.

  • Good Manufacturing Practice or “GMP” means the current good manufacturing practices applicable from time to time to the manufacturing of a Product or any intermediate thereof pursuant to Applicable Law.

  • Marijuana-infused products means products that contain marijuana or marijuana extracts and are intended for human use. The term "marijuana-infused products" does not include useable marijuana.

  • Good Laboratory Practices or “GLP” means the then-current good laboratory practice standards promulgated or endorsed by the FDA, as defined in U.S. 21 C.F.R. Part 58 (or such other comparable regulatory standards in jurisdictions outside the United States, as they may be updated from time to time).

  • Distillery manufacturing license means a license issued in accordance with