Toimialayhteisöt

 

 

This document specifies methods for evaluating the stability and buoyancy of intact (i.e. undamaged) craft. The flotation characteristics of craft susceptible to swamping are also encompassed. The evaluation of stability and buoyancy properties using this document will enable the craft to be assigned to a design category (A, B, C or D) appropriate to its stability and buoyancy characteristics. This document is principally applicable to small craft propelled primarily by sail (even if fitted with an auxiliary engine) of 2,5 m up to and including 24 m hull length. In relation to habitable multihulls, this document includes assessment of susceptibility to inversion, definition of viable means of escape and requirements for inverted flotation. This document excludes: — inflatable and rigid-inflatable craft covered by the ISO 6185 series; — aquatic toys; — gondolas and pedalos; — surfboards including sailing surfboards; and — hydrofoils and foil stabilized craft when not operating in the displacement mode. NOTE Displacement mode means that the craft is only supported by hydrostatic forces. This document does not include or evaluate the effects on stability of towing, fishing, or lifting operations or dynamic stability of high speed craft, which can be separately considered if appropriate. It only considers normal operation of the craft, but unattended craft issues are out of scope

 

This document provides examples of specifications, defines evaluation methodologies and requirements for labelling methods for recycled man-made fibres in the supply chain,including relevant supporting information. Recycling technologies covered will include physical, mechanical, and chemical recycling methods applied within the supply chain, together with associated supporting information.

 

This document specifies the design, minimum safety requirements, and inspection and testing procedures for liquefied hydrogen (LH2) marine transfer arms intended for use at onshore LH2 terminals handling LH2 carriers. It also covers the minimum requirements for safe LH2 transfer between ship and shore. Although the requirements for power/control systems are covered, this document does not include all of the details for the design and fabrication of standard parts and fittings associated with transfer arms. This document is mainly focused on hard pipe type transfer systems; hose type transfer systems are not described in detail in the general description of this document. However, hose type transfer systems can also be considered as reasonable vacuum insulated technology for the design of transfer arms for liquefied hydrogen.

 

This document establishes a vocabulary for high-pressure pipes and end-connections in fuel injection systems for diesel (compression-ignition) engines. The terms defined in this document are required precisely for high-pressure pipes and end-connections in fuel injection systems. Terms and definitions relating to other fuel injection equipment are found in the other parts of the ISO 7876 series. NOTE When the word “fuel” is used in the terms listed it can be omitted providing there can be no misunderstanding.

 

This document specifies process and quality requirements for the biobanking of mammalian (including human) cell lines. It describes requirements for the fundamental procedures of the biobank handling cell lines, such as establishment, reception, identification, propagation, preservation, storage, quality control, and distribution of cell lines. This document can be used by organizations performing biobanking activities with mammalian cell lines used for research and development, biobank users, organizations and schemes using peer-assessment and accreditation bodies. This document does not apply to biological material intended for therapeutic use. NOTE International, national or regional regulations or requirements can also apply to specific topics covered in this document.

 

This International Standard specifies the functional requirements and principles for design, operation and requalification of pipelines in the petroleum and natural gas industries using reliability-based limit state methods as permitted by ISO 13623. Reliability-based limit state methods provide a systematic way to predict pipeline safety in design and operation. This International Standard supplements ISO 13623 and can be used in cases where ISO 13623 does not provide specific guidance and where limit states methods can be applied, such as, but not limited to, — qualification of new concepts, e.g. when new technology is applied or for design scenarios where industry experience is limited, — re-qualification of the pipeline due to a changed design basis, such as service-life extension or change of the transported fluid, which can include reduced or increased uncertainties due to improved integrity monitoring and operational experience or limited information on pipeline properties relevant to the new service — collapse under external pressure in deep water, — extreme loads, such as seismic loads (e.g. at a fault crossing), ice loads (e.g. by impact from ice keels), — situations where strain-based criteria can be appropriate. This document applies to rigid metallic pipelines on-land and offshore used in oil and gas industries including lower carbon energy.

 

This document specifies a test method for determining the watertightness under dynamic pressure of curtain walling, as defined in iso:proj:73332ISO 22497:2021 , including fixed and openable infills as shown in Figure 1 , assembled for normal use and installed as in practice. This document is applicable to areas subject to driving rain and strong wind, including typhoons, hurricanes, and cyclones. This document does not apply to the joints between curtain walling perimeter frame and the building construction as shown in Figure 2 .

 

This document defines the set of requirements for the architecture of a system that processes, manages and communicates electronic health record (EHR) information: an EHR architecture. The requirements are formulated to ensure that these EHRs are faithful to the needs of healthcare delivery, are clinically valid and reliable, are ethically sound, meet prevailing legal requirements, support good clinical practice and facilitate data analysis for a multitude of purposes. This document does not specify the full set of requirements that need to be met by an EHR system for direct patient care or for other use cases, but the requirements defined by this International Standard do contribute to the governance of EHR information within such systems.

 

This document specifies requirements for the biobanking of human and mouse pluripotent stem cells (PSCs), including the collection of biological source material and associated data, establishment, expansion, characterization, quality control (QC), maintenance, preservation, storage, thawing, disposal, distribution and transport. This document is applicable to all organizations performing biobanking with human and mouse PSCs used for research and development. This document does not apply to cell lines used for in vivo application in humans, clinical applications or therapeutic use. NOTE International, national or regional regulations or requirements, or multiple of them, can also apply to specific topics covered in this document.

 

This document describes a field method for measuring the surface profile produced by any of the abrasive blast-cleaning procedures given in ISO 8504-2:2019 [1] . The method uses replica tape and a suitable gauge for measuring the roughness of a surface before the application of paint or another protective coating. The method is applicable within the range of profile heights cited for a given grade (or thickness) of replica tape. The commercial grades currently available permit measurement of average peak-to-valley profiles of 12 µm to 150 µm. The method is valid for surfaces that have been cleaned with abrasives.

 

ISO 8503-5:2017 describes a field method for measuring the surface profile produced by any of the abrasive blast-cleaning procedures given in ISO 8504-2. The method uses replica tape and a suitable gauge for measuring, on site, the roughness of a surface before the application of paint or another protective coating. The method is applicable within the range of profile heights cited for a given grade (or thickness) of replica tape. The commercial grades currently available permit measurement of average peak-to-valley profiles of 20 µm to 115 µm. The method is valid for surfaces that have been cleaned with abrasives.

 

This document specifies the requirements and corresponding test methods for a biocompatible and bio-inert ceramic bone-substitute material based on yttriastabilized tetragonal zirconia (yttria tetragonal zirconia polycrystal, Y-TZP) for use as a material for surgical implants.

 

ISO 16708:2006 specifies the functional requirements and principles for design, operation and re-qualification of pipelines in the petroleum and natural gas industries using reliability based limit state methods as permitted by ISO 13623. Reliability-based limit state methods provide a systematic way to predict pipeline safety in design and operation. ISO 16708:2006 supplements ISO 13623 and can be used in cases where ISO 13623 does not provide specific guidance and where limit states methods can be applied, such as, but not limited to - qualification of new concepts, e.g. when new technology is applied or for design scenarios where industry experience is limited, - re-qualification of the pipeline due to a changed design basis, such as service-life extension, which can include reduced uncertainties due to improved integrity monitoring and operational experience, - collapse under external pressure in deep water, - extreme loads, such as seismic loads (e.g. at a fault crossing), ice loads (e.g. by impact from ice keels), - situations where strain-based criteria can be appropriate. ISO 16708:2006 applies to rigid metallic pipelines on-land and offshore used in the petroleum and natural gas industries.

 

This document specifies a method for the determination of extractable metals in leather using extraction with an acid artificial-perspiration solution and subsequent determination with inductively coupled plasma optical emission spectrometry (ICP-OES), inductively coupled plasma mass spectrometry (ICP-MS), atomic absorption spectrometry (AAS) or spectrometry of atomic fluorescence (SFA). This method determines extractable metals in leather; it is not compound-specific or specific to the oxidation state of the metals. This method is especially suitable for determining the extractable chromium in chromium-tanned leathers.

 

This document specifies requirements for the production and quality control of immunomagnetic beads. This document also gives general quality attributes for immunomagnetic beads, together with common methods for evaluating these quality attributes for end-use. This document is applicable to the research and development of immunomagnetic beads, and to the application field of immunomagnetic beads, e.g., cell sorting, protein purification, and microbial separation. NOTE For manufacturing of cell-based therapeutic products, users can refer to applicable standards such as ISO 20399 [1].

 

This document specifies requirements for the biobanking of bacteria and archaea. It includes management of microbial material associated data as well as biosafety and biosecurity requirements. This document is applicable to all organizations performing biobanking with bacteria and archaea used for research and development. This document does not apply to processing methods for microbial materials intended for food/feed production, laboratories undertaking food/feed analysis or therapeutic use. NOTE International, national or regional regulations or requirements, or multiple of them, can also apply to specific topics covered in this document.

 

This document provides requirements for the biobanking of helminths as parasitic resources including the collection, safeguarding, classification, proliferation, preservation, storage and distribution of helminths. This document sets requirements for the quality of helminths and their associated data, the data collection, and safety management when handling the helminths as a source of human disease infection. This document is applicable to all organizations performing biobanking with helminths used for research and development. NOTE International, national or regional regulations or requirements, or multiple of them, can also apply to specific topics covered in this document.

 

This document specifies a method for the determination of chemical components of titanium (Ti), vanadium (V), tungsten (W), molybdenum (Mo), silicon (Si), and aluminium (Al) in selective catalytic reduction (SCR) catalyst and intermediates by wavelength dispersive X-ray Fluorescence spectrometer (WD-XRF).

 

This document specifies the method for the digestion of different plant biostimulants with aqua regia to enable a subsequent determination of arsenic (As), cadmium (Cd), copper (Cu), chromium (Cr), mercury (Hg), nickel (Ni), lead (Pb) and zinc (Zn). The method can be also applied for determination of other elements. The method is applicable for all solid and/or liquid plant biostimulants. This document is applicable to the blends of fertilizing products where a blend is a mix of at least two of the following component EU fertilising products categories: Fertilizers, Liming Materials, Soil Improvers, Growing Media, Inhibitors, Plant Biostimulants, and where the following category Plant Biostimulants is the highest % in the blend by mass or volume, or in the case of liquid form by dry mass. If Plant Biostimulants is not the highest % in the blend, the this Standard for the highest % of the blend applies. In case a blend of fertilizing products is composed of components in equal quantity or in case the component EU fertilising products used for the blend have identical formulations11 An example of such a blend is a product with two claimed functions consisting of a non-microbial plant biostimulant and an organic fertilizer composed of 1 kg/kg of plant biostimulant from seaweed., the user decides which standard to apply. The digests are suitable for analysis using ISO 37701-2:2026(ICP-AES) and ISO 37701-3:2026(Hg analysis). NOTE Alternatively, inductively coupled plasma mass spectrometry (ICP-MS) can be used for the determination of the elements in the aqua regia digests if the user proves that the method gives the same results.