Toimialayhteisöt

 

This document specifies a method for the determination of pH of a solution of ammonium nitrate fertilizer of high nitrogen content. This document is applicable to the fertilizing products blends where a blend is a mix of at least two of the following components: fertilizers, liming materials, soil improvers, growing media, inhibitors, plant biostimulants, and where the following category: inorganic fertilizers is the highest % in the blend by mass or volume, or in the case of liquid form by dry mass. If inorganic fertilizer is not the highest % in the blend, the European Standard for the highest % of the blend applies. In case a fertilizing product blend is composed of components in equal quantity, the user decides which standard to apply. Variations in analytical methods for fertilizing product blends can lead to differing results as some components or matrix interactions can affect the outcome. Validation procedures have shown that developed standard methods are robust and reliable across diverse product compositions, but possible interferences and unexpected results when analysing fertilizing product blends are possible.

 

This document specifies a method for the determination of the copper content in ammonium nitrate fertilizers of high nitrogen content. This document is applicable to the fertilizing products blends where a blend is a mix of at least two of the following components: fertilizers, liming materials, soil improvers, growing media, inhibitors, plant biostimulants, and where the following category: inorganic fertilizers is the highest % in the blend by mass or volume, or in the case of liquid form by dry mass. If inorganic fertilizer is not the highest % in the blend, the European Standard for the highest % of the blend applies. In case a fertilizing product blend is composed of components in equal quantity, the user decides which standard to apply. Variations in analytical methods for fertilizing product blends can lead to differing results as some components or matrix interactions can affect the outcome. Validation procedures have shown that developed standard methods are robust and reliable across diverse product compositions, but possible interferences and unexpected results when analysing fertilizing product blends are possible.

 

This document specifies a method for the determination of the chloride content in ammonium nitrate fertilizers of high nitrogen content. This document is applicable to the fertilizing products blends where a blend is a mix of at least two of the following components: fertilizers, liming materials, soil improvers, growing media, inhibitors, plant biostimulants, and where the following category: inorganic fertilizers is the highest % in the blend by mass or volume, or in the case of liquid form by dry mass. If inorganic fertilizer is not the highest % in the blend, the European Standard for the highest % of the blend applies. In case a fertilizing product blend is composed of components in equal quantity, the user decides which standard to apply. Variations in analytical methods for fertilizing product blends can lead to differing results as some components or matrix interactions can affect the outcome. Validation procedures have shown that developed standard methods are robust and reliable across diverse product compositions, but possible interferences and unexpected results when analysing fertilizing product blends are possible.

 

This document is applicable to liming materials, which contain oxides, hydroxides, carbonates or silicates of the nutrients calcium (Ca) or magnesium (Mg) and the function of which is to correct soil acidity. This document is applicable to the fertilizing products blends where a blend is a mix of at least two of the following components fertilizers, liming materials, soil improvers, growing media, inhibitors, plant biostimulants and where the following category liming materials is the highest % in the blend by mass or volume, or in the case of liquid form by dry mass. If liming materials is not the highest % in the blend, the European Standard for the highest % of the blend applies. In case a fertilizing product blend is composed of components in equal quantity, the user decides which standard to apply. Variations in analytical methods for fertilizing product blends can lead to differing results as some components or matrix interactions can affect the outcome. Validation procedures have shown that developed standard methods are robust and reliable across diverse product compositions, but possible interferences and unexpected results when analysing fertilizing product blends are possible. In case of chromium VI determination, in a fertilizing product blend containing organic matter, the European Standard for liming materials and inorganic fertilizers is not applicable. This document specifies references to the methods for the determination of the following physical and chemical properties and specific contaminants in liming materials: — determination of the cadmium content; — determination of the chromium VI content; — determination of the mercury content; — determination of the nickel content; — determination of the lead content; — determination of the arsenic content; — determination of the total chromium content; — determination of neutralizing value; — determination of the reactivity; — determination of the grain size/granulometry; — determination of the total CaO content; — determination of the total MgO content; — determination of the dry matter content; — determination of the copper and zinc content; — determination of the phosphonates content. — determination of the chloride content; — determination of quantity (indicated by mass or volume).

 

This document specifies a common framework for audit trails for electronic health records (EHR), in terms of audit trigger events and audit data, to keep the complete set of personal health information auditable across information systems and domains. It is applicable to systems processing personal health information that create a secure audit record each time a user reads, creates, updates, or archives personal health information via the system. NOTE       Such audit records at a minimum uniquely identify the user, uniquely identify the subject of care, identify the function performed by the user (record creation, read, update, etc.), and record the date and time at which the function was performed. This document covers only actions performed on the EHR, which are governed by the access policy for the domain where the electronic health record resides. It does not deal with any personal health information from the electronic health record, other than identifiers, the audit record only containing links to EHR segments as defined by the governing access policy. It does not cover the specification and use of audit logs for system management and system security purposes, such as the detection of performance problems, application flaw, or support for a reconstruction of data, which are dealt with by general computer security standards such as ISO/IEC 15408 (all parts)[9]. Annex A gives examples of audit scenarios. Annex B gives an overview of audit log services.

 

This document outlines the concepts and principles for information management at a stage of maturity described as "building information modelling (BIM) according to the ISO 19650 series". This document provides recommendations for a framework to manage information including exchanging, recording, versioning and organizing for all actors. This document is applicable to the whole life cycle of any built asset, including strategic planning, initial design, engineering, development, documentation and construction, day-to-day operation, maintenance, refurbishment, repair and end-of-life. This document can be adapted to assets or projects of any scale and complexity, so as not to hamper the flexibility and versatility that characterize the large range of potential procurement strategies and so as to address the cost of implementing this document.

 

This document specifies requirements for information management, in the form of a management process, within the context of the delivery phase of assets and the exchanges of information within it, using building information modelling. This document can be applied to all types of assets and by all types and sizes of organizations, regardless of the chosen procurement strategy.

 

The classification method in this part of ISO 4433 is used to determine the chemical resistance of pipes, fittings and valve components made of PVC-U, PVC-HI, PVC-M, PVC-A, PVC-O and PVC-C designed for the transport of chemicals in the absence of pressure and stresses, such as earth loads and dynamic internal stresses. To determine chemical resistance, the method uses the change in mass and changes in tensile properties that result from storing test pieces, taken from such pipes, fittings and valve components, in chemicals. The test is performed in accordance with ISO 4433-1. This part of ISO 4433 is also applicable to PVC-U, PVC-HI, PVC-M, PVC-A, PVC-O and PVC-C sheets, as appropriate.

 

The method of classification given in this part of ISO 4433 serves to determine the chemical resistance of polyolefin pipes, fittings and valve components designed for the conveyance of chemicals in the absence of pressure and stress such as earth loads, dynamic internal stresses. To determine the chemical resistance, the method uses the change in mass and the changes in tensile properties which result from the storage of test pieces, taken from such pipes, fittings and valve components, in chemicals. The test is carried out in accordance with ISO/DIS 4433-1. This part of ISO 4433 is also applicable to polyolefin sheets as appropriate.

 

This part of ISO 4433 specifies a method for carrying out a preliminary evaluation of the behaviour of thermoplastics pipes, fittings, sheets and valve components in relation to the chemicals transported. This method provides information on the suitability of pipes, fittings, sheets and valve components for transporting chemicals in the absence of pressure or stresses such as earth loads, dynamic stresses and internal stresses. NOTE An additional indication about test method to evaluate the compatibility of plastic materials against liquids, gases, their mixtures or multiphase fluids is reported in ISO 23936-1[11]. A full procedure for carrying out the test is also reported in ISO 175, which is devoted to plastics in general, and not specifically to thermoplastics pipes, fittings, sheets and valve components. Fatigue resistance, permeability, resistance to rapid gas decompression are not taken into account in this document.

 

This part of ISO 15534 specifies current requirements for human body measurements (anthropometric data) that are required by ISO 15534-1 and ISO 15534-2 for the calculation of access-opening dimensions as applied to machinery. The anthropometric data originates from static measurements of nude people and does not consider body movements, clothing, equipment, machinery-operating conditions, or environmental conditions. The data are based on information from anthropometric surveys representative of worldwide population groups, including both men and women, as specified in ISO 7250–3. Measurements are provided, as required by ISO 15534-1 and ISO 15534-2, for the 5th, 95th, and 99th percentiles of the relevant population group worldwide.

 

This part of ISO 15534 specifies the dimensions of openings for access into machinery as defined in EN ISO 12100. It provides the dimensions to which the values given in ISO 15534-3 are applicable. Values for additional space requirements are given in Annex A. This part of ISO 15534 has been prepared primarily for non-mobile machinery; there may be additional specific requirements for mobile machinery. Dimensions for access openings are based on the values for the 95th percentile, whereas reach distances are based on the values for the 5th percentile, in each case the least favourable body dimension of the expected user population being used as a basis. The same considerations apply to the location of access openings. The anthropometric data provided in ISO 15534-3 originate from static measurements of nude persons and do not consider body movements, clothing, equipment, machinery-operating conditions, or environmental conditions. This part of ISO 15534 shows how to combine the anthropometric data with suitable allowances to account for these factors. Situations where people are to be prevented from reaching a hazard are dealt with in ISO 13857.

 

This part of ISO 15534 specifies the dimensions of openings for whole-body access into machinery as defined in ISO 12100. It provides the dimensions to which the values given in ISO 15534-3 are applicable. Values for additional space requirements are given in Annex A. This part of ISO 15534 has been prepared primarily for non-mobile machinery; however, there may be additional specific requirements for mobile machinery. Dimensions for passages are based on the values for either the 95th or the 99th percentiles of the expected user population. Values for the 99th percentile apply to emergency egress routes. The anthropometric data provided in ISO 15534-3 originate from static measurements of nude persons and do not take into account body movements, clothing, equipment, machinery-operating conditions, or environmental conditions. This part of ISO 15534 illustrates how to combine the anthropometric data with suitable allowances to account for these factors. Situations where people are to be prevented from reaching a hazard are addressed in ISO 13857 - Safety distances to prevent hazard zones being reached by upper and lower limbs.

 

This document defines the design, safety and operation characteristics of gaseous hydrogen land vehicle (GHLV) refuelling connectors. GHLV refuelling connectors consist of the following components, as applicable: — receptacle and protective cap (mounted on vehicle); — nozzle; — communication hardware. This document is applicable to refuelling connectors which have nominal working pressures or hydrogen service levels up to 70 MPa and having flow capacities greater than 120 g/s. This document is not applicable to refuelling connectors dispensing blends of hydrogen with natural gas.

 

The method of classification given in this part of ISO 4433 serves to determine the chemical resistance of PVDF and ECTFE pipes, fittings and valve components designed for the conveyance of fluids in the absence of pressure and stress (e.g. due to earth loads or traffic loads, dynamic or internal stresses). To determine the chemical resistance, the method uses the change in mass and the changes in tensile properties which result from the storage of test pieces in chemicals. The storage test is carried out in accordance with ISO/DIS 4433-1. This part of ISO 4433 is also applicable to PVDF and ECTFE sheets as appropriate

 

This document specifies how to perform hardness measurements at other then surrounding or standard laboratory temperatures. This procedure is ment for measurements at lower temperatures as well as those at elevated temperatures. In the annex a test based on hardness measurements for determining the progressive stiffening of rubber with time, caused by crystallization is given

 

This document defines methods for the measurement of periodic, random and transient mechanical vibration, as well as vibration containing regular or occasional shocks. It indicates the principal factors that combine to determine the degree to which a vibration exposure will be acceptable. Informative Annex B, Annex C, and Annex D indicate current opinion and provide guidance on the possible effects of vibration on health, comfort and perception and motion sickness. The frequency range considered is 0,5 Hz to 80 Hz for health, comfort and perception 0,1 Hz to 0,5 Hz for motion sickness. Although the potential effects on human performance are not covered, most of the guidance on whole-body vibration measurement also applies to this area. This document also defines the principles of preferred methods of mounting transducers for determining human exposure. It does not apply to the evaluation of extreme-magnitude single shocks such as those that occur in vehicle accidents. This document is applicable to motions transmitted to the human body as a whole through the supporting surfaces: the feet of a standing person, the buttocks, back and feet of a seated person or the supporting area of a recumbent person. This type of vibration is found in vehicles, in machinery, in buildings and in the vicinity of working machinery. As mentioned, this document does not address the effects of vibration transmitted directly to the limbs (e.g. by power tools, hand-operated vehicle controls and steering wheels).

 

This document specifies a common framework for audit trails for electronic health records (EHR), in terms of audit trigger events and audit data, to keep the complete set of personal health information auditable across information systems and domains. It is applicable to systems processing personal health information that create a secure audit record each time a user reads, creates, updates, or archives personal health information via the system. NOTE Such audit records at a minimum uniquely identify the user, uniquely identify the subject of care, identify the function performed by the user (record creation, read, update, etc.), and record the date and time at which the function was performed. This document covers only actions performed on the EHR, which are governed by the access policy for the domain where the electronic health record resides. It does not deal with any personal health information from the electronic health record, other than identifiers, the audit record only containing links to EHR segments as defined by the governing access policy. It does not cover the specification and use of audit logs for system management and system security purposes, such as the detection of performance problems, application flaw, or support for a reconstruction of data, which are dealt with by general computer security standards such as ISO/IEC 15408 [2] all parts. Annex A gives examples of audit scenarios. Annex B gives an overview of audit log services.

 

Tämä kansallinen standardi sisältää toimivuusvaatimukset sairaaloiden tai vastaavien hoitoyksiköiden potilaiden tai asukkaiden käyttöön tarkoitetuille pussilakanoille, lakanalle ja tyynyliinalle. Standardissa määritellään materiaalien oleelliset ominaisuudet ja minimi vaatimustaso sekä annetaan oleelliset tuotteiden mitat.

Huom. standardiehdotuksen taulukossa 5 on virhe. Oikeat mitat ovat: 
Leveys 160 cm (toleranssi 150...165 cm) x pituus 290 cm (toleranssi 280...300 cm).
Virhe korjataan ennen standardin vahvistamista SFS-standardiksi.