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;
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Manufacturing of pharmaceutical products means one or more of the following activities—
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Manufacturing of pharmaceutical products means an activity that
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Examples of Manufacturing of pharmaceutical products in a sentence

  • Manufacturing of pharmaceutical products The chemical synthesis, fermentation, extraction, formulation and finishing of pharmaceutical products and, where carried out at the same site, the manufacture of intermediate products.

  • The Directorate of Drug Administration (DDA)The Manufacturing of pharmaceutical products is regulated by international standards.

  • Manufacturing of pharmaceutical products The chemical synthesis, fermentation, extraction, formulation and finishing of pharmaceutical products and, where car­ ried out at the same site, the manufacture of intermediate products.

  • Manufacturing of pharmaceutical products (> 50) 20 (1) 5 (2) 15 (2) 5 % of solvent input 15 % of solvent input (1) If techniques are used which allow reuse of recovered solvent, the emission limit value in waste gases shall be 150.

  • Manufacturing of pharmaceutical products The chemical synthesis, fermentation, extraction, formulation and finishing of pharmaceutical products and, where carried out at the same site, the manufacture of intermediate products Not Applicable9.

  • 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).

  • Helen aims to achieve carbon neutral energy production by 2035 and wind power is one of the ways to achieve the target.

  • 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.

  • 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.

  • The water management association also had an ambition to develop a “Vision plan” for the Lyckeby river (Visionsplan).

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” means the active pharmaceutical or biological ingredient as further set forth in the applicable Product Manufacturing Plan.

  • 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:

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

  • Diagnostic clinical procedures manual means a collection of written procedures that describes each method (and other instructions and precautions) by which the licensee performs diagnostic clinical procedures; where each diagnostic clinical procedure has been approved by the authorized user and includes the radiopharmaceutical, dosage, and route of administration.

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

  • Manufacturing Process means any process for—

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

  • API means American Petroleum Institute.

  • 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, set forth in this Agreement, required to manufacture Product or Products from Active Materials and Components;

  • 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

  • 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.

  • processed products means goods placed under a processing procedure which have undergone processing operations;

  • 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.