Manufacturing of pharmaceutical products definition

Manufacturing of pharmaceutical products means chemical synthesis, fermentation, extraction, formulation and finishing of pharmaceutical products and, where carried out at the same site, the manufacture of intermediate products;
Sample 1Sample 2Sample 3
Manufacturing of pharmaceutical products means one or more of the following activities—
Sample 1Sample 2Sample 3
Manufacturing of pharmaceutical products means an activity that
Sample 1Sample 2

Examples of Manufacturing of pharmaceutical products in a sentence

  • Manufacturing of pharmaceutical products requires adherence to standards of Good Manufacturing Practice (GMP) to ensure “that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization” (World Health Organization, Expert Committee on Specifications for Pharmaceutical Preparations: 2003).

  • Each JMC member shall have appropriate seniority and sufficient expertise in the Manufacturing of pharmaceutical products similar to the Products to make decisions within the scope of the JMC’s responsibility.

  • Manufacturing of pharmaceutical products shall mean the industrial manufacture of phar- maceutical mixtures, the chemical synthesis, fermentation, extraction, formulation and finishing of bulk drug substances, and, where this takes place at the same site, the manu- facture of intermediate products in accordance with the Medicines Act (395/1987).

  • The JMC shall include individuals from each Party with reasonable expertise in the area of Manufacturing of pharmaceutical products.

  • The Group’s turnover comprises the following: For the six months ended 30 September 20142013(Unaudited)(Unaudited)HK$’000HK$’000 Manufacturing of pharmaceutical products 16,307 28,846Trading of pharmaceutical products58,00140,766 74,308 69,612 Detailed segment information is presented by way of the Group’s primary segment reporting basis, which is by business segment.

Related to Manufacturing of pharmaceutical products

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

  • Biological product means a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, protein other than a chemically synthesized polypeptide, or analogous product, or arsphenamine or any derivative of arsphenamine or any other trivalent organic arsenic compound, applicable to the prevention, treatment, or cure of a disease or condition of human beings.

  • 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”).

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Finished Products means any one or more of the following petroleum oils, or a mixture or combination of these oils, to be used without further processing except blending by mechanical means:

  • New Products means any product which is not an Enhanced Product or 2 Existing Product but which is substantially similar to an Existing Product with respect to design and function and possesses reasonable performance improvements. If Company desires to purchase an Enhanced or New Product(s) from Supplier, Company shall so notify Supplier and provide Supplier the opportunity to manufacture such Enhanced or New Product(s), subject to the following conditions and procedures.

  • Aerosol Product means a pressurized spray system that dispenses product ingredients by means of a propellant contained in a product or a product's container, or by means of a mechanically induced force. “Aerosol Product” does not include “Pump Spray.”

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

  • Hemp products means all products made from industrial hemp,

  • Manufacturing Process means any process for—

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • API means the American Petroleum Institute.

  • Manufacturing Know-How means all information, techniques, inventions, discoveries, improvements, practices, methods, knowledge, skill, experience and other technology, whether or not patentable or copyrightable, and any copyrights based thereon, relating to or necessary or useful for the production, purification, packaging, storage and transportation of Collaboration Products, including without limitation specifications, acceptance criteria, manufacturing batch records, standard operating procedures, engineering plans, installation, operation and process qualification protocols for equipment, validation records, master files submitted to the FDA, process validation reports, environmental monitoring processes, test data including pharmacological, toxicological and clinical test data, cost data and employee training materials.

  • Commercial Product means any such product as defined in FAR 2.101.

  • Manufacturing Services means the manufacturing, quality control, quality assurance, stability testing, packaging, and related services, as set forth in this Agreement, required to manufacture Product or Products using the Active Materials, Components, and Xxxx Back Items;

  • Interchangeable biological product means a biological product that the federal Food and Drug Administration has:

  • Drug Product means a specific drug in dosage form from a known source of manufacture, whether

  • 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.

  • Marihuana-infused product means a topical formulation, tincture, beverage, edible substance, or similar product containing marihuana and other ingredients and that is intended for human consumption.

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

  • Manufacturing means all activities related to the manufacture of a Compound, including planning, purchasing, manufacture, processing, compounding, storage, filling, packaging, waste disposal, labeling, leafleting, testing, quality assurance, sample retention, stability testing, release, dispatch and supply, as applicable.

  • Reference biological product means the single biological product licensed pursuant to 42 U.S.C.

  • Products means information resources technologies that are, or are related to, EIR.

  • Product Manufacturer means the entity that assembles the component parts to manufacture the final Product;

  • Medical marijuana product means a product that contains cannabinoids that have been extracted from plant material or the resin therefrom by physical or chemical means and is intended for administration to a licensed patient, including but not limited to concentrates, oils, tinctures, edibles, pills, topical forms, gels, creams, and other derivative forms, except that this term does not include live plant forms.