Toimialayhteisöt

 

This document specifies a laboratory method of determining the pentachlorophenol content of wood. The method is applicable to all types of pentachlorophenol (PCP) in woods and wood-based materials as well as for the analysis of waste timber with respect to its pentachlorophenol (PCP) content. The method described has a measurement range from 250 µg/kg up to pentachlorophenol (PCP) contents of 5 mg/kg of dry matter. These figures refer to the given example (where an aliquot of 1 ml of the extract is used for acetylation, see 9.3). NOTE 1 If lower quantification limits are required, a higher volume of extract aliquot can be used for derivatisation. NOTE 2 This method could have some modifications with some wood species as hardwoods. In general, in the case of complex matrix, a method using mass spectrometry can be used.

 

ISO 12401:2009 specifies the requirements for performance, sizing, marking and test methods for deck safety harnesses and safety lines on recreational craft. It is applicable to harnesses and lines in the following sizes of body mass (multisizing is permitted): size 1: > 50 kg ; size 2: > 20 kg = 50 kg; size 3: = 20 kg; which are intended to be worn by all persons when in the exposed cockpit or on the working deck of a craft afloat. It is not applicable to dinghy 'trapeze' harnesses, windsurfing harnesses, seat harnesses for fast motor boats, and harnesses intended to protect against falls from a height.

 

This International Standard specifies the conditions for determination of tensile properties (including tensile modulus, Poisson’s ratio, strength, strain at maximum force and fracture strain) of ceramic matrix composite materials with continuous fibre reinforcement at room temperatures. This International Standard applies to all ceramic matrix composites with a continuous fibre reinforcement, including unidirectional (1D), bi-directional (2D), and multi-directional (xD, with x > 2), reinforcement, loaded along a principal axis of reinforcement.

 

This document provides a generic description of the methods available for measuring soil characteristics and indicators of core ecological soil functions. No distinction of context is made, i.e. no differentiation of land use and management (e.g agricultural, forest, urban, natural or contaminated lands). For each ecological soil function, the document specifically lists biotic and abiotic characteristics that can be measured. It focuses on characteristics and indicators that are either available as ISO documents or published in peer-reviewed papers. This document applies to ecological soil functions and is not applied to soil functions such as geotechnical functions (foundation support for buildings, tunnels, etc.) or geothermal functions. Indeed, ecosystem services do not address soils without a topsoil, or with a covered topsoil (buildings, infrastructure, greenhouse farming, solar panel parks). Methods and indicators for ecological soil functions can help in the assessment of soil-related ecosystem services but the overall assessment of ecosystem services is not covered in this document. Other methods based on proxy indicators (e.g. soil occupation, hydrography parameters) can also be used for land planning at large scale. These indicators are not included in this document.

 

This document specifies a method for the determination of the tensile strength, tensile modulus of elasticity and strain at the maximum force of a resin-impregnated yarn specimen at ambient temperature. This method is applicable to yarns of ceramic fibres that are used as reinforcements in composite materials. The test results obtained by this method are applicable for quality control and comparison of the ceramic fibres. The outputs of this method are not to be mixed up with the strength of filaments derived from tensile tests on dry tows specified in ISO 22459.

 

 

This document specifies a method for the determination of the water vapour transmission rate (often erroneously called “permeability”) of sheet materials. This method is not generally recommended for use if the transmission rate is expected to be less than 1 g/m2 per day or for materials thicker than 3 mm. In such cases the method specified in ISO 9932 is preferred. The method cannot be applied to materials that change dimensionally (shrink or expand) to an appreciable extent under the test conditions used. In the case of materials that are damaged by hot wax, only mechanically-sealed test dishes can be used. For some purposes it may be necessary to determine the transmission rate of creased material; a procedure for this is given in Annex B.

 

Tämän standardin tarkoitus on standardin SFS-EN 5973 mukaisista hirsistä valmistettujen rakennusten hirsirakenteiden ja niiden osien laatuvaatimusten määrittely. Tämä standardi koskee rakennuksissa käytettäviä kuusesta (Picea abies) ja männystä (Pinus sylvestris) valmistettuja, perinteisiä massiivi- ja lamellihirsirakenteita, sekä painumattomia hirsirakenteita, joita voidaan rakentaa kaikenlaiseen loma-, asuin- ja julkiseen käyttöön. Tämän standardin mukaisia hirsirakenteita voidaan käyttää joko kantavina tai kevyinä seinärakenteina. Tämä standardi ei kata palonsuojakäsiteltyjä eikä erilaisin menetelmin lahonsuojattuja hirsirakenteita ja -rakennuksia. Tämä standardi kattaa hirsirakenteet, joissa hirret ovat pintakäsitelty kemiallisilla suoja-aineilla hyönteisiä tai värimuutoksia vastaan, mikäli nämä käsittelyt eivät vaikuta hirsien ja hirsirakennusten muihin ominaisuuksiin.

 

This document specifies a method using light microscopy for the differentiation of the colouration process of fabrics, between dyeing or printing with pigments and, dyeing or printing with dyes. This document is applicable to coloured fabrics with the exception of those made of fibres coloured by melt or dope dyeing.

 

This document specifies an extension of evaluation methods and activities for cryptographic protocols based on ISO/IEC 15408-4 that provides a framework for evaluation methods and activities. This document provides a mapping between the work items for cryptographic protocol evaluation and the associated evaluation activities or evaluation methods. Additionally, this document also provides security assurance classification based on the cryptographic assessment performed by automated provers in four different levels of increasing assurance.

 

This document is intended to provide specific levels of information relevant to the identification of a Pharmaceutical Product or groups of Pharmaceutical 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 the product lifecycle to support pharmacovigilance, regulatory and other activities worldwide. In addition, this document is essential to ensure that pharmaceutical product information is assembled in a structured format with transmission between a diverse set of stakeholders for both regulatory and clinical (e.g. e-prescribing, clinical decision support) purposes. This ensures interoperability and compatibility for both the sender and the recipient. This document is not intended to be a scientific classification for pharmaceutical products. Rather, it is a formal association of particular data elements categorised in prescribed combinations and uniquely identified when levelling degrees of information are incomplete. This allows for Pharmaceutical Products to be unequivocally identified on a global level. References to other normative IDMP standards and specifications for data exchange mechanisms for pharmaceutical product information are included in Clause 2, to be applied in the context of this document. Medicinal products for veterinary use are out of scope of this document.

 

This document defines terms, gives guidance for classification and establishes requirements for nucleic acid- and protein-based bio-devices. This document is applicable to bio-devices incorporating natural, modified and synthetically derived nucleic acid and/or protein. This document does not apply to medical devices or products.

 

This document provides a scheme for the assessment of conformity of PVC-U products and assemblies for the rehabilitation of existing pipelines, in accordance with ISO 11300-3, and intended to be included in the manufacturer’s quality plan as part of the quality management system and for the establishment of certification procedures.

 

In this document, a test sample is dissolved in water, and the dilution of the solution is to a known mass. The solution is nebulized into an inductively coupled plasma/atomic emission spectrometer (ICP-OES), and the intensity of the emitted light from metal ions is measured simultaneously. This document is applicable to the determination of impurity metal ions such as aluminium (Al), calcium (Ca), cadmium (Cd), chromium (Cr), copper (Cu), iron (Fe), potassium(K), magnesium (Mg), sodium (Na), nickel (Ni), lead (Pb) and zinc (Zn) in lithium hexafluorophosphate (LiPF6). The method is suitable for mass concentrations of impurity metallic ions in LiPF6 below 10 mg/kg. The scope of this method may be extended to higher mass concentrations of impurity metallic ions in LiPF6 if it can be shown that additionally occurring interferences are considered and corrected for carefully. It is up to the user to demonstrate the fitness for purpose.

 

ISO 14644-15:2017 provides requirements and guidelines for assessing the chemical airborne cleanliness of equipment and materials which are foreseen to be used in cleanrooms and associated controlled environments which are linked to the ISO standard for cleanliness classes by chemical concentration (see ISO 14644-8). The following are outside the scope of ISO 14644-15:2017: - health and safety requirements; - compatibility with cleaning agents and techniques; - cleanability; - biocontamination; - specific requirements of equipment and materials for processes and products; - design details of equipment.

 

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 the product lifecycle to support pharmacovigilance, regulatory and other activities worldwide. In addition, ISO 11616:2017 is essential to ensure that pharmaceutical product information is assembled in a structured format with transmission between a diverse set of stakeholders for both regulatory and clinical (e.g. e-prescribing, clinical decision support) purposes. This ensures interoperability and compatibility for both the sender and the recipient. ISO 11616:2017 is not intended to be a scientific classification for pharmaceutical products. Rather, it is a formal association of particular data elements categorised in prescribed combinations and uniquely identified when levelling degrees of information are incomplete. This allows for Medicinal Products to be unequivocally identified on a global level. References to other normative IDMP and messaging standards for pharmaceutical product information are included in Clause 2, to be applied in the context of ISO 11616:2017. Medicinal products for veterinary use are out of scope of ISO 11616:2017.

 

 

This document specifies business requirements for processes intended to preserve digital data. NOTE Data are stored and maintained for the purpose of retrievability and usability during the required archiving period. In addition, for the purpose of some business requirements, data are authentically preserved and accessed. This document is intended to allow for different implementations based on a company’s specific business environment. This document is not intended to incorporate company specific requirements and does not dictate specific organizational structures within a company. This document does not specify a design or an implementation of an archive system. Actual implementations can distribute responsibilities or break out functionality differently. This document assumes that all requirements for configuration management of the product data are in place and therefore are not specifically described in this document.

 

This document is applicable only to harnesses for paragliders. The intermediate attachment system between the harness and the paraglider / the emergency parachute does not form part of this document. This document specifies safety requirements and test methods.

 

This document provides the performance specifications and requirements for wood-based panels used in continuously fully supported non-structural floating floors.