Synthesized pharmaceutical manufacturing definition

Synthesized pharmaceutical manufacturing means manufacture of pharmaceutical products by chemical synthesis.
Synthesized pharmaceutical manufacturing means manufacture of pharmaceutical products by one or more chemical reactions followed by a series of purifying operations. Organic chemicals are used as raw materials and as solvents.
Synthesized pharmaceutical manufacturing means manufacture of pharmaceutical products and intermediates by chemical synthesis. The production and recovery of materials produced via fermentation, extraction of organic chemicals from vegetative materials or animal tissues, and formulation and packaging of the product are not considered synthesized pharmaceutical manufacturing.

Examples of Synthesized pharmaceutical manufacturing in a sentence

  • Synthesized pharmaceutical manufacturing process is any process involving the manufacture of pharmaceutical products and intermediates by chemical synthesis.

  • Apply a thin coating of silicone grease to both halves of the transducer housing where the housing will contact the pipe.

  • Synthesized pharmaceutical manufacturing facility” means a facility in which drugs are produced by means of chemical synthesis.(J) As used in paragraph (X) of rule 3745-21-09 of the Administrative Code (pertaining to rubber tire manufacturing facilities) and in rules 3745-21-04 and 3745-21-10 of the Administrative Code: (1) “Bead dipping” means the dipping of an assembled tire bead into a solvent based cement.

  • Specific mechanisms include extraction, centrifugation, filtration, and crystallization; (v) "Synthesized pharmaceutical manufacturing" means manufacture of pharmaceutical products by chemical synthesis.

  • Specific mechanisms include extraction, centrifugation, filtration, and crystallization.2.5 "Synthesized pharmaceutical manufacturing" means manufacture of pharmaceutical products and intermediates by chemical synthesis.

  • Synthesized pharmaceutical manufacturing" means manufacture of pharmaceutical products and intermediates by chemical synthesis.

  • A fundamental study of this kind would be crucial to rationalize the design of different nano-drug delivery systems for mucosal administration and predict their performance in vivo, which may reduce the drug attrition rates [28].


More Definitions of Synthesized pharmaceutical manufacturing

Synthesized pharmaceutical manufacturing means manufacture of pharmaceutical products and intermediates by chemical synthesis. The production and recovery of materials produced via fermentation, extraction of organic chemicals from vegetable materials or animal tissues, and formulation and packaging of the product is not covered by this regulation.
Synthesized pharmaceutical manufacturing means manufacture of pharmaceutical products by chemical synthesis. (b) This Regulation applies to synthesized pharmaceutical products manufacturing facilities. (c) The owner or operator of a synthesized pharmaceutical products manufacturing facility shall control the emissions of volatile organic compounds from:(1) reactors, distillation operations, crystallizers, centrifuges, and vacuum dryers that have the potential to emit 15 pounds per day or more of volatile organic compounds with surface condensers that meet the requirements of Paragraph (e) of this Regulation or equivalent controls;(2) air dryers and production equipment exhaust system by reducing emissions of volatile organic compounds:
Synthesized pharmaceutical manufacturing means manufacture of pharmaceutical products by
Synthesized pharmaceutical manufacturing means manufacture of “pharmaceutical products and intermediates” by chemical syntheses. The production and recovery of materials produced via fermentation, extraction of organic chemicals from vegetative
Synthesized pharmaceutical manufacturing means manufacture of pharmaceutical products of chemical synthesis.
Synthesized pharmaceutical manufacturing means manufacture of “pharmaceutical products and intermediates” by chemical syntheses. The production and recovery of materials produced via

Related to Synthesized pharmaceutical manufacturing

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

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

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

  • Manufacturing Technology means any and all patents, patent applications, Know-How, and all intellectual property rights associated therewith, and including all tangible embodiments thereof, that are necessary or useful for the manufacture of adeno- associated viruses, adeno-associated virus vectors, research or commercial reagents related thereto, Licensed Products, or other products, including manufacturing processes, technical information relating to the methods of manufacture, protocols, standard operating procedures, batch records, assays, formulations, quality control data, specifications, scale up, any and all improvements, modifications, and changes thereto, and any and all activities associated with such manufacture. Any and all chemistry, manufacturing, and controls (CMC), drug master files (DMFs), or similar materials provided to regulatory authorities and the information contained therein are deemed Manufacturing Technology.

  • Manufacturing Process means any process for—

  • 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.

  • Active Pharmaceutical Ingredient or “API” means the active pharmaceutical substance of the Drug in bulk form prior to incorporation into the Product.

  • 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;

  • 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.

  • Manufacturing Know-How means, with respect to the Product or any Variant thereof, the technology, data, designs, processes, methods, specifications and other know-how used in connection with the formulation, manufacture, labeling, packaging, quality control, release testing, and production of the Product, and all ingredients used therein and portions thereof.

  • 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.

  • Hemp products means all products made from industrial hemp,

  • 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.

  • Distillery manufacturing license means a license issued in accordance with

  • API means the American Petroleum Institute.

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Bioassay means the determination of kinds, quantities or concentrations and, in some cases, the locations of radioactive material in the human body, whether by direct measurement, in vivo counting, or by analysis and evaluation of materials excreted or removed from the human body. For purposes of these rules, “radiobioassay” is an equivalent term.

  • 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.

  • in vitro diagnostic medical device means any medical device which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, equipment, software or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue donations, derived from the human body, solely or principally for the purpose of providing information:

  • Investigational Medicinal Product means the study drug or control material as defined in the Protocol.

  • Manufacturing Facility means buildings and structures, including machinery and equipment, the primary purpose of which is or will be the manufacture of tangible goods or materials or the processing of such goods or materials by physical or chemical change.

  • Commercialization or “Commercialize” means activities directed to marketing, promoting, research and development as required, manufacturing for sale, offering for sale, distributing, importing or selling a product, including sub-licensing or sub-contracting of these activities.

  • 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;

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

  • Hemp product means the same as that term is defined in § 3.2-4112.

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