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ISO 28593:2017 specifies a system of single sampling schemes for lot-by-lot inspection by attributes. All the sampling plans of the present system are of accept-zero form, i.e. no lot is accepted if the sample from it contains one or more nonconforming items. The schemes depend on a suitably-defined average outgoing quality limit (AOQL), the value of which is chosen by the user; no restrictions…

ISO 18322:2017 specifies requirements for when a space test centre needs to demonstrate its competence to consistently provide space testing that meets customer requirements. It specifies requirements for space test centres, applicable to the test process, test personnel (both, of the customer and the space test centre), test facilities, test environment and any operations related to the test…

ISO 19634:2017 defines the symbols to be used to represent physical, mechanical and thermal characteristics, as determined by methods described in relevant ISO publications, for ceramic matrix composites. It is aimed at avoiding confusion in reporting measurements and characteristics of products. Where possible, the definitions are in accordance with the relevant parts of ISO 80000. In addition,…

ISO 11616:2017 is intended to provide specific levels of information relevant to the identification of a Medicinal Product or group of Medicinal Products. It defines the data elements, structures and relationships between data elements that are required for the exchange of regulated information, in order to uniquely identify pharmaceutical products. This identification is to be applied throughout…

ISO 11615:2017 establishes definitions and concepts and describes data elements and their structural relationships, which are required for the unique identification and the detailed description of Medicinal Products. Taken together, the standards listed in the Introduction define, characterise and uniquely identify regulated Medicinal Products for human use during their entire life cycle, i.e.…

ISO/TS 20443:2017 defines concepts and describes data elements and their structural relationships, which are required for the unique identification and the detailed description of Medicinal Products. Taken together, all ISO IDMP standards (ISO 11615, ISO 11616, ISO 11238, ISO 11239 and ISO 11240) define, characterise, and uniquely identify regulated Medicinal Products for human use from approval…

ISO/TS 20451:2017 defines the concepts required to associate pharmaceutical products with an appropriate set of PhPID(s) in accordance with ISO 11616. Pharmaceutical identifiers and elements are to represent pharmaceutical products as represented in a Medicinal Product as indicated by a Medicines Regulatory Authority. The suite of ISO IDMP standards can be applied to off-label usage of Medicinal…

The purpose of this document is intended to establish the certification requirements, rules of procedure and marking requirements applying to the certification of polyethylene (PE) pipe and fittings according to the requirements of the product standards BNQ 3624-027, BNQ 3624-110, BNQ 3624-115, BNQ 3624-120 and ASTM F894. It is important to note that, to meet the needs expressed by prime…

ISO 18888:2017 specifies standard rules for preparing, conducting, evaluating and reporting thermal performance tests on combined cycle and cogeneration power plants driven by gas turbines for base and part load operation with or without supplementary firing. ISO 18888:2017 is applicable to - thermal performance tests for general information, - thermal acceptance tests for determining…

ISO 18237:2017 specifies: - test equipment, test circuit and a procedure for the evaluation of the water separation capabilities of a dehydrator; - a procedure for preparing test fluid; - a procedure for obtaining and analysing the test fluid samples. ISO 18237:2017 applies only to those dehydration units that can dry a hydraulic fluid to less than 20 % of the hydraulic fluid'…