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ISO 9000:2015 describes the fundamental concepts and principles of quality management which are universally applicable to the following: organizations seeking sustained success through the implementation of a quality management system; customers seeking confidence in an organization's ability to consistently provide products and services conforming to their requirements; organizations seeking confidence in their supply chain that their product and service requirements will be met; organizations and interested parties seeking to improve communication through a common understanding of the vocabulary used in quality management; organizations performing conformity assessments against the requirements of ISO 9001; providers of training, assessment or advice in quality management; developers of related standards. ISO 9000:2015 specifies the terms and definitions that apply to all quality management and quality management system standards developed by ISO/TC 176.

 

ISO 4259-1:2017 specifies the methodology for the design of an Interlaboratory Study (ILS) and calculation of precision estimates of a test method specified by the study. In particular, it defines the relevant statistical terms (Clause 3), the procedures to be adopted in the planning of ILS to determine the precision of a test method (Clause 4), and the method of calculating the precision from the results of such a study (Clauses 5 and 6). The procedures in ISO 4259-1:2017 have been designed specifically for petroleum and petroleum related products, which are normally considered as homogeneous. However, the procedures described in ISO 4259-1:2017 can also be applied to other types of homogeneous products. Careful investigations are necessary before applying ISO 4259-1:2017 to products for which the assumption of homogeneity can be questioned.

 

This document specifies design requirements for non-powered access installed on cranes. NOTE 1 For other type of access, a requirement for information to be supplied is specified. Slidable, retractable means of access are excluded from the scope, except movable hoop guards. This document covers means of access to control stations and all access required for maintenance, certain erection and dismantling operations. For those cranes which are intended to be erected and dismantled frequently to change their places of work, specific requirements for the access needed during these operations are not covered by this document and can be given in the appropriate European Standards for specific crane types. Lighting of means of access is not covered by this document and can be given in the appropriate European Standards for specific crane types. NOTE 2 Specific requirements for access on particular types of cranes are given in the appropriate European Standard for the particular crane type. The requirements given in this document do not take into account the safety distances related to: - guarding against hazard from moving parts; - relative movement between crane and adjacent structure or the ground/floor; - hazardous surface temperature; - electrical equipment. The significant hazards covered by this document are identified in Annex A. This document is not applicable to cranes manufactured before the date of its publication.

 

This document specifies two methods of indicating the composition of yarns, whether single, folded, cabled or multiple wound. The notation comprises linear density indicated in the Text System, number of filaments in filament yarns, direction and amount of twist, and number of folds. This document is not applicable to some special kinds of yarns, for example to fancy yarns, textured or bulked yarns or yarns produced by wrapping a textile or non-textile material round a core; nor is it applicable to yarns with other features such as constituent fibres, after treatment and type of package.

 

 

ISO 4259-2:2017 specifies the methodology for the application of precision estimates of a test method derived from ISO 4259-1. In particular, it defines the procedures for setting the property specification limits based upon test method precision where the property is determined using a specific test method, and in determining the specification conformance status when there are conflicting results between supplier and receiver. Other applications of this test method precision are briefly described in principle without the associated procedures. The procedures in ISO 4259-2:2017 have been designed specifically for petroleum and petroleum-related products, which are normally homogeneous. However, the procedures described in ISO 4259-2:2017 can also be applied to other types of homogeneous products. Careful investigations are necessary before applying ISO 4259-2:2017 to products for which the assumption of homogeneity can be questioned.

 

ISO 18739:2016 specifies terms, synonyms for terms and definitions used in the process chain for CAD/CAM systems in dentistry.

 

This document specifies requirements for fire activated oxygen shut-off devices that stop the flow of oxygen in respiratory therapy tubing when activated by fire. NOTE 1        Typical arrangements for fire activated oxygen shut-off devices are shown in Annex C. NOTE 2        Respiratory therapy tubing is covered by ISO 17256. NOTE 3        Use of fire activated oxygen shut-off devices in medical devices or accessories is not mandated in this document. The fire activated oxygen shut-off devices specified in this document are not suitable for use with oxygen therapy systems with flows in excess of 20 l/min). NOTE 4        There is rationale for this clause in A.2. The requirements in this device-specific standard take precedence over any conflicting requirements in the general standard for airway devices (ISO 18190). All the common requirements that appear in the general standard for airway devices have been removed from this document.

 

This document defines key terminology, establishes circular economy principles at the levels of construction works as well as construction products of all kinds, and provides a guidance framework for the implementation and assessment of circularity in the built environment.

 

1.1 Purpose This document establishes the minimum requirements for the qualification and certification of personnel performing non-destructive testing (NDT), nondestructive inspection (NDI), or nondestructive evaluation (NDE) in the aerospace manufacturing, service, maintenance and overhaul industries. For the purposes of this document, the term NDT will be used and will be considered equivalent to NDI and NDE. In Europe, the term "approval" is used to denote a written statement by an employer that an individual has met specific requirements and has operating approval. The term "certification" as defined in 3.2 is used throughout this document as a substitute for the term "approval". Except when otherwise specified in the written practice, certification in accordance with this document includes operating approval. 1.2 Applicability This document applies to personnel who: - use NDT methods or equipment to test and/or accept materials, products, components, assemblies or sub-assemblies; - are directly responsible for the technical adequacy of the NDT methods and equipment used; - operate automatic interpretation or evaluation systems; - approve NDT procedures or work instructions; - audit NDT facilities; or - provide technical NDT support or training. This document does not apply to individuals who only have administrative or supervisory authority over NDT personnel or to research personnel developing NDT technology for subsequent implementation and approval by a certified Level 3. See Clause 8 regarding applicability to personnel performing specialized inspections using certain direct readout instruments. Definition Automated equipment refers to machinery and systems designed to perform tasks without human intervention. In a completely automated industrial process, these systems operate independently to execute various functions. 1.2.1 Implementation This document addresses the use of a National Aerospace NDT Board (NANDTB). NANDTBs are only used as specified per Annex C and it is not mandatory to have such a board for compliance with this document. Personnel certified to previous revisions of NAS410 or EN 4179 need not recertify to the requirements of this document until their current certification expires. 1.3 Methods 1.3.1 NDT methods This document contains detailed requirements for the following NDT methods: Eddy Current Testing (ET) Liquid Penetrant Testing (PT) Magnetic Particle Testing (MT) Radiographic Testing (RT) Shearography Testing (ST) Thermographic Testing (IRT) Ultrasonic Testing (UT) 1.3.2 Other methods When invoked by engineering, quality, cognizant engineering organization or prime contractor requirements, this document applies to other current and emerging NDT methods used to determine the acceptability or suitability for intended service of a material, part, component, sub-assembly or assembly. Such methods include, but are not limited to, acoustic emission, neutron radiography, leak testing, and holography.

 

The base nomenclature provided in IEEE 11073 to support terminology for implantable cardiac devices is extended in this standard. Devices within the scope of this nomenclature are implantable devices such as pacemakers, defibrillators, devices for cardiac resynchronization therapy, and implantable cardiac monitors. The discrete terms necessary to convey a clinically relevant summary of the information obtained during a device interrogation are defined in this nomenclature. To improve workflow efficiencies, cardiology and electrophysiology practices require the management of summary interrogation information from all vendor devices and systems in a central system such as an Electronic Health Records (EHR) system or a device clinic management system. To address this requirement, the Implantable Device, Cardiac (IDC) Nomenclature defines a standard-based terminology for device data. The nomenclature facilitates the transfer of data from the vendor proprietary systems to the clinic EHR or device clinic management system.

 

This document specifies a method for the enumeration of culturable microorganisms in water by counting the colonies on a low-nutrient agar culture medium by spread plate inoculation after incubation at 22 °C for 7 d. The method is intended to measure the operational efficiency of the treatment process of public drinking water supplies, including the water in distribution systems and containers. The method is particularly suitable to monitor water for human consumption which is low in nutrients and is distributed in temperatures below 20 °C (Reference [1]). The method can be applied to all types of water, including pool and spa waters. The low-nutrient agar in use in this document usually gives higher colony counts from water samples than nutrient-rich formulations of culture media typically used for enumeration of culturable microorganisms (References [2], [3], [4]).

 

This document specifies a method of measuring the burning velocity (BV) of slowing burning refrigerants (< 10 cm/s) for use with other standards that utilize the BV for determining safety classification of refrigerants (e.g. ISO 817) or that use the BV in establishing requirements on the use of slow burning refrigerants (e.g. ISO 5149).

 

This document, within the context of methods’ and tools’ capability for supporting product line texture: This document does not concern the processes and capabilities of tools and methods for a single system but rather deals with those for a family of products.

 

This document, within the context of methods and tools that support adoption, construction, operation, and management of product line maturity framework, This document does not concern the processes and capabilities of methods and tools for a single system but rather deals with those for a family of products.

 

 

This document specifies the general requirements and provides guidance for the development and application of loop-mediated isothermal amplification (LAMP) to detect microorganisms and associated genetic markers (e.g. antimicrobial resistance genes, virulence genes) in the food chain. This document is applicable to all LAMP methods, platforms, items from food chain and laboratories. The use of LAMP for quantification is out of scope for this document. Validation and verification of LAMP methods as either alternative or reference methods are not covered in this document. Both validation and verification of microbiological methods are discussed in detail in the ISO 16140 series and ISO 17468. General requirements for isothermal methods including LAMP for molecular biomarker analysis are covered by ISO 22942-1, and general requirements and definitions for polymerase chain reaction (PCR) for the detection and quantification of microorganisms in the food chain are covered by ISO 22174. This document has been established for microorganisms in the food chain and is applicable to:

 

This document specifies the classification of imperfections likely to be generated during an additive manufacturing process by DED for metallic parts. This document also indicates the most probable causes of the formation of imperfections and includes illustrations. Acceptance criteria for imperfections are not included in this document.

 

This document specifies dimensions required for the installation and integration of the high pressure fuel pump in gasoline (GDI) engines. The location of the fuel connections and the dimensions of the pump outside shape are not defined since they vary according to the manufacturer of the pump and to the application.