Good Manufacturing Practise = Regulations on the safety and quality in manufacturing pharmaceutical preparations
The value added by the productive sectors before deduction of depreciation. GMP excludes the value of services in the nonproductive sectors such as defense, public administration, finance, education, health, and housing. Also known as social product.
Good Manufacturing Practice, implementation regulation concerning the manufacturing and quality control of pharmaceutical products.
Good Manufacturing Practice, a system of guidelines to ensure manufacturing quality
Good Manufacturing Practices: That part of the pharmaceutical quality assurance, which ensures that products are consistently produced and controlled in conformity with quality standards appropriate for their intended use and as required by the product specification.
The FDA Good Manufacturing Practice (GMP) Regulation governing the quality system requirements for products regulated under the FDA. The GMP pertaining to medical devices is set out in the Quality System Regulation, Part 820 of 21 CFR.
Good Manufacturing Practice: in the pharmaceutical context,these are the requirements covering all aspects of pharmaceutical manufacture, including chemical and microbiological testing of raw materials and products.
Good Manufacturing Practice: US FDA requirements for pharmaceutical production (includes laboratory practice)
Good Manufacturing Practice. A system for ensuring that products are consistently produced and controlled according to quality standards.
Good Manufacturing Practices (GMP) for food additives are described in Section 3.3 of the Preamble of the Codex General Standard for Food Additives as follows:"All food additives subject to the provisions of this Standard shall be used under conditions of good manufacturing practice, which include the following: the quantity of the additive added to food shall be limited to the lowest possible level necessary to accomplish its desired effect; the quantity of the additive that becomes a component of food as a result of its use in the manufacturing, processing or packaging of a food and which is not intended to accomplish any physical, or other technical effect in the food itself, is reduced to the extent reasonably possible; and, the additive is prepared and handled in the same way as a food ingredient."
Good Manufacturing Practices (as established by the FDA).
the Good Manufacturing Practice, which are guidelines and regulations from time to time issued by health authorities relating to quality control in the production of pharmaceutical products
Good Manufacturing Practice. guidelines ensuring the quality and purity of chemical products that are intended for use in pharmaceutical applications, and controls ensuring that methods and facilities used for production, processing, packaging, and storage result in drugs with consistent and sufficient quality, purity, and activity.
Good Manufacturing Practice. Set of regulations and guidelines controlling the quality of manufacturing operations aimed at ensuring consistency of product quality in order to ensure patient safety.
A methodology of specification for a manufacturing process that ensures quality, safety, and engineering tolerances are met.
GMP Facility Good Automated Manufacturing Practices
Good manufacturing practice. A set of principles and procedures which, when followed by manufacturers of therapeutic goods, helps ensure that the products manufactured will have the required quality.
Good Manufacturing Practice. Standardized procedures required by regulatory authorities to ensure consistent and safe production of a therapeutic product.
Good management practices
Good Manufacturing Practice. A set of principles and procedures that, when followed by manufacturers of drugs and other therapeutics, helps ensure that the products manufactured will be of the required quality. GMP is based on the premise that quality cannot be tested into a batch but must be built into each batch of product during all stages of manufacturing. See also current Good Manufacturing Practice.
Good Manufacturing Practice. Established and regulated way of working with regard to the production of, for example, medical device products.
Good Manufacturing Practices in the pharmaceutical industry, as defined by regulatory authorities. In silico Performed by way of computer analysis. In vitro Performed in a test tube or other laboratory apparatus. In vivo Performed in a living organism.
Good Manufacturing Process
Good manufacturing practice: that part of the measures taken to ensure the quality of investigatory or medicinal products concerned with consistent and controlled production
Good Manufacturing Practice. A quality assurance system for the manufacture of therapeutic goods based on best international practice.
Good Manufacturing Practices. Good Manufacturing Practices are standard guidelines set out by the FDA to ensure drug development is carried out in safe and quality processes, to avoid contamination and ensure repeatability.
Good Manufacturing Practices, a code of manufacturing practices published by both the TPD and FDA to which pharmaceutical manufacturers must adhere.
Good Manufacturing Practice – a system designed to prevent hazards in food packaging processes.
is that part of QA which ensures that products are consistently produced and controlled to the quality standards appropriate to the intended use and as required by the marketing authorisation, product specification or
