Solid dosage forms definition

Solid dosage forms means capsules or tablets intended for oral administration.
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Examples of Solid dosage forms in a sentence

  • Solid dosage forms should be wetted in a small amount of soapy water before tipping everything into the general medicines waste bin.

  • Primary and or Secondary Packaging only E.1 Liquid dosage formsE.2 Semi-solid dosage formsE.2 Solid dosage forms F.

  • Water activity testing is conducted as follows to determine the type of product for assigning the default BUD: • Solid dosage forms (i.e., tablets and capsules): No water activity testing is necessary.

  • Solid dosage forms to be separated from liquids and internal preparations to be separated from external preparations.

  • Solid dosage forms such as tablets are commonly procured in bulk and repackaged in developing countries in order control costs and therefore to ensure that governments are able to provide medicines to a large majority of the population.

  • Implication of quantitative selection of each excipient in product development.2. Drug-excipient interaction: Drug-excipient interaction and incompatibilities, physical, chemical, pharmaceutical and therapeutic, analytical techniques to characterize drug excipient incompatibility.3. Solid dosage forms: Tablets, benefits, improved tablet production, advances in materials, material handling and granulation;process automation.

  • Banks are using the technology to deliver their service since it saves cost, and uses as a competitive advantage to support their service with new developments, helps them to be accessible with the unbanked population through different delivery channels.

  • Solid dosage forms removed from delivery container and placed in collection barrel.

  • USP <1111> MICROBIOLOGICAL EXAMINATION OF NONSTERILE PRODUCTS: ACCEPTANCE CRITERIA FOR PHARMACEUTICAL PREPARATIONS AND SUBSTANCES FOR PHARMACEUTICAL USE434 Potentially Reducing Microbiological Release Testing for Solid Dosage Forms Based on Risk-435 Based Impact Assessment 436437 Solid dosage forms with a water activity that will not support vegetative microbial growth are438 excellent candidates for reduced microbial testing for product release and stability.

  • Regulatory basis, Validation of sterile products; Solid dosage forms, Process Validation and non-sterile Analytical method validation.

Related to Solid dosage forms

  • 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;

  • Civil Aeronautical Product means any civil aircraft, aircraft engine, or propeller or subassembly, appliance, material, part, or component to be installed thereon.

  • Final Product means a product that is not used in producing other products and is built and intended for use outdoors, provided the final product has not deteriorated or has otherwise become a potential source of contaminants.

  • 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.

  • Red Hat Products means Software, Services, Subscriptions and other Red Hat branded offerings made available by Red Hat.

  • Therapeutic diet means meals served that are soft, low-fat, low-sodium or controlled calorie.

  • Inert ingredient means an ingredient which is not an active ingredient.

  • 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”).

  • Food and food ingredients means substances, whether in liquid, concentrated, solid, frozen, dried, or dehydrated form, that are sold for ingestion or chewing by humans and are consumed for their taste or nutritional value. Food and food ingredients do not include alcoholic beverages and tobacco.

  • 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.

  • Tobacco products means cigars, cigarettes, cheroots, stogies, periques, granulated, plug cut, crimp cut, ready rubbed, and other smoking tobacco, snuff, snuff flour, moist snuff, cavendish, ping and twist tobacco, fine-cut and other chewing tobaccos, shorts, refuse scraps, clippings, cuttings and sweepings of tobacco, and other kinds and forms of tobacco, prepared in such manner as to be suitable for chewing or smoking in a pipe or otherwise, or both for chewing and smoking.

  • 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:

  • 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.

  • Therapeutic school means a residential group living facility:

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

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

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

  • 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.

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

  • Labeling means all labels and other written, printed, or graphic matter on an article or any of its

  • 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.

  • GMPs means all good manufacturing practices under Title 21 of the United States Code of Federal Regulations, as amended from time to time.

  • API means American Petroleum Institute.

  • Licensed Products means tangible materials which, in the course of manufacture, use, sale, or importation, would be within the scope of one or more claims of the Licensed Patent Rights that have not been held unpatentable, invalid or unenforceable by an unappealed or unappealable judgment of a court of competent jurisdiction.

  • Licensed Services means all functions performed by the Licensed System.

  • Marijuana products means concentrated marijuana products and marijuana products that are comprised of marijuana and other ingredients and are intended for use or consumption, such as, but not limited to, edible products, ointments, and tinctures.