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This document specifies the determination of fluoroquinolone residue content in meat, fish and their products by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method. This document is applicable to the determination of enrofloxacin, ciprofloxacin, norfloxacin, ofloxacin and pefloxacin residues in meat, fish and their products, including livestock and poultry.

This document specifies a test method for estimating the magnitude of radiosonde temperature sensor warming, induced by direct solar radiation, based on variations in air pressure, temperature, ventilation speed, tilt angle of its supporting sensor boom, and light illumination angle on the boom through a laboratory evaluation. This document provides the following: technical requirements for a laboratory setup to measure the effect of direct solar radiation on radiosonde temperature measurement under simulated sounding conditions; a test procedure for estimating radiosonde temperature measurement errors due to direct solar radiation in the air pressure range of 3 hPa to 1 000 hPa, temperature range1) of −70 °C to 50 °C, ventilation speed range of 3 m∙s−1 to 7 m∙s−1 at a specified irradiance (e.g. 1 000 or higher), sensor boom tilt range2) from 0° to 45° with respect to the air ventilation direction and the range of light illumination3) angle from 0° to 90° with respect to the sensor boom plane; a method to evaluate uncertainty in the results under the test conditions.

This document specifies, with reference to ISO 230-1 and ISO 230-2, geometric tests and tests for checking the accuracy and repeatability of positioning of numerically controlled axes for general purpose, normal accuracy, bridge-type milling machines with a fixed bridge (portal type). This document also specifies the applicable tolerances corresponding to the above-mentioned tests. This document is applicable to machines with moving tables and fixed double columns. It does not include single-column (open sided) machines and those with fixed tables and moving columns. This document deals only with the verification of the accuracy of the machine. It does not apply to the testing of the machine operation (vibration, abnormal noise, stick-slip motion of components, etc.) nor to machine characteristics (such as speeds, feeds, etc.), which are generally checked before testing the accuracy. This document provides the terminology used for the principal components of the machine and the designation of the axes with reference to ISO 841.

This document specifies a liquid chromatography tandem mass spectrometry (LC-MS/MS) method for the determination of marker residues of nicarbazin (4,4-dinitrocarbanilide) in chicken tissue and eggs. This document is applicable to the determination of marker residues of nicarbazin (4,4-dinitrocarbanilide) in chicken tissue (including muscle, liver and kidney) and eggs.

This document specifies a procedure for determining whether a perceptible sensory difference or similarity exists between samples of two products. The method is a forced-choice procedure. The method is applicable whether a difference exists in a single sensory attribute or in several attributes. The method is statistically less efficient than the triangle test (described in ISO 4120) but is easier to perform by the assessors. The method is applicable even when the nature of the difference is unknown (i.e. it determines neither the size nor the direction of difference between samples, nor is there any indication of the attribute(s) responsible for the difference). The method is applicable only if the products are fairly homogeneous. The method is effective for: determining that either: a perceptible difference results (duo-trio testing for difference); or a meaningful perceptible difference does not result (duo-trio testing for similarity) when, for example, a change is made in ingredients, processing, packaging, handling or storage; selecting, training and monitoring assessors. Two forms of the method are described: the constant-reference technique, used when one product is familiar to the assessors (e.g. a sample from regular production); the balanced-reference technique, used when one product is not more familiar than the other.

This document provides requirements for the evaluation process for bottles predominantly made of PET with respect to compatibility of the design with recycling processes.
Packaging components and ancillary elements made of other materials than PET are also covered by this document as they need to be evaluated for compatibility with the recycling processes.

This document provides requirements for the evaluation process of any flexible packaging with the main body of the packaging unit predominantly made of PE or PP and for the evaluation process of separate components predominantly made of flexible PE or flexible PP, with respect to compatibility of the design with state-of-the-art collecting, sorting and recycling processes, and the characterization of the output(s) compared to a reference material.
Packaging constituents and packaging components made of other materials than PE and PP are also covered by this document as they need to be evaluated on compatibility with PE or PP polymer recycling.

IEC 61512-1:2026 applies to systems, specifications, and their use for implementing batch and related procedure-oriented manufacturing controls in the process industries. This document establishes a reference model framework for procedure-oriented control, defines terms to help explain the model relationships and usage, and describes general criteria for evaluating conformance. This follows the principle of separation between recipe procedural elements and equipment procedural elements enabling operations to define recipes without the need of changes in equipment procedures.
This second edition cancels and replaces the first edition published in 1997. This edition constitutes a technical revision.
This edition includes the following significant technical changes with respect to the previous edition:
a) Models and text are modified to provide more detail and clarity. Key clarifications are:
1) Two types of equipment modules are defined: generic and recipe-aware. All recipe-aware equipment modules contain procedural control and can be used as phases in the recipe.
2) Execution of all procedural control contained directly in units is part of the Unit Supervision activity.
3) The relationships between types of recipes, recipe components, and equipment control are more fully described and illustrated.
4) Entity relationship diagrams have been replaced with more intuitive UML instance diagrams, except for the equipment entity model.
5) The transition diagram for the procedural states example has been updated with a more intuitive and complete UML state diagram.
6) References to other standards in the series and to IEC 62264 are included to provide direction for further clarification of selected topics.
7) Activity names are capitalised to help prevent confusion with similar terms, such as their underlying functions.
b) Previous Clauses 4 through 6 (now Clauses 4 through 8) were rearranged to provide a clearer top-down organisation of the document. Key changes are:
1) Removing the lower levels of the physical (role-based equipment) model (see 4.4.2) to eliminate redundancy because their groupings are defined by the associated functionality in the equipment entity model and are not meaningful for batch control without those associations.
2) Describing equipment control and the equipment entity model immediately after the physical (role-based equipment) model and describing each level as completely as possible without excessive use of forward references (see 4.4.3).
3) Combining the descriptions of basic, procedural, and coordination control with their usage in each type of equipment entity, providing a single consolidated discussion of each type of control (see Clause 5)
4) Additional considerations to support application of the models have been grouped in Clause 7 to clarify their supporting relationship to the core models.
c) Clause 9 was added to define completeness, compliance, and conformance in relation to this document.
d) Annex B was added to provide a more expansive procedural state reference model. The model found in Clause 7 can be considered a collapsed version of this more general model.
e) Annex C was added to clarify a number of points concerning the models, their application, and the new Clause 9 on conformance and compliance.
f) Annex E was added to more fully describe the changes in this update to IEC 61512-1:1997.

This document covers the design of any rigid packaging with the main body of the packaging unit predominantly made of PS or XPS and the design of separate components predominantly made of rigid PS or XPS with respect to compatibility of the design with state-of-the-art collecting, sorting and recycling processes and useability of the recyclates in an application.
Packaging constituents and packaging components made of other materials than PS and XPS are also covered by this document as they need to be evaluated on compatibility with PS or XPS polymer recycling.

This document specifies good clinical practice (GCP) for the design, conduct, recording and reporting of clinical investigations carried out in human subjects to assess the clinical performance or effectiveness and safety of medical devices.
For post-market clinical investigations, the principles set forth in this document are intended to be followed as far as relevant, considering the nature of the clinical investigation (see Annex I).
This document specifies the general requirements intended to
protect the rights, safety and well-being of human subjects, users or other persons,
ensure the scientific conduct of the clinical investigation and the credibility of the clinical investigation results,
define the responsibilities of the sponsor and principal investigator, and
assist sponsors, investigators, ethics committees, regulatory authorities and other bodies involved in the conformity assessment of medical devices.
Other standards or national requirements can also apply to the investigational device(s) under consideration or the clinical investigation(s).
NOTE            For Software as a Medical Device (SaMD), where appropriate, demonstration of the analytical validity (the SaMD’s output is accurate for a given input), the scientific validity (the SaMD’s output is associated to the intended clinical condition/physiological state), and clinical performance (the SaMD’s output yields a clinically meaningful association to the target use) of the SaMD, the requirements of this document apply as far as relevant (see Reference [5]). Justifications for exemptions from this document can consider the uniqueness of indirect contact between subjects and the SaMD.
This document does not apply to in vitro diagnostic medical devices. However, there can be situations, dependent on the device and national or regional requirements, where users of this document can consider whether either specific sections or requirements of this document, or both, can be applicable.

IEC 61788-15:2026 describes measurements of the intrinsic surface impedance (Zs) of HTS films at microwave frequencies by a modified two-resonance mode dielectric resonator method. The object of measurement is to obtain the temperature dependence of the intrinsic Zs at the resonant frequency f0.
The frequency and thickness range and the measurement resolution for the Zs of HTS films are as follows:
- frequency: up to 40 GHz;
- film thickness: greater than 50 nm;
- measurement resolution: 0,01 mΩ at 10 GHz.
It is crucial that the Zs data at the measured frequency, and that scaled to 10 GHz be reported for comparison, assuming the f2 rule for the intrinsic surface resistance, Rs (f < 40 GHz), and the f rule for the intrinsic surface reactance, Xs. This second edition cancels and replaces the first edition published in 2011. This edition constitutes a technical revision.
This edition includes the following significant technical changes with respect to the previous edition:
- informative Annex B, combined relative standard uncertainty in the intrinsic surface impedance is added;
- the terms, ‘precision and accuracy’, are replaced with uncertainty;
- results from a round robin test are added.

This document specifies requirements and test methods for male condoms made from natural rubber latex.
This document does not specify requirements related to any medicinal substances applied to or delivered by the condom.
NOTE            The safety and effectiveness of any medicinal substance are assessed according to national and regional regulations.

This document provides guidelines for the use of hydrogen in its gaseous and liquid forms as well as its storage in either of these or other forms (hydrides). This document identifies the basic safety concerns, hazards and risks, and describes the properties of hydrogen that are relevant to safety. Detailed safety requirements associated with specific hydrogen applications are treated in separate International Standards.
“Hydrogen” in this document means protium (the most common isotope of hydrogen) (1H), not deuterium (2H) or tritium (3H).

This document applies to the basic safety and essential performance of pulse oximeter equipment intended for use on humans, hereafter referred to as ME equipment. This includes any part necessary for normal use, including the pulse oximeter monitor, pulse oximeter probe, and probe cable extender.
These requirements apply to pulse oximeter equipment, including pulse oximeter monitors, pulse oximeter probes and probe cable extenders regardless of their origin (i.e. including remanufactured products).
The intended use of pulse oximeter equipment includes, but is not limited to, the estimation of arterial oxygen haemoglobin saturation and pulse rate of patients in professional healthcare institutions as well as patients in the home healthcare environment and the emergency medical services environment.
If a clause or subclause is specifically intended to be applicable to ME equipment only, or to ME systems only, the title and content of that clause or subclause says so. If that is not the case, the clause or subclause applies both to ME equipment and to ME systems, as relevant.
Hazards inherent in the intended physiological function of ME equipment or ME systems within the scope of this document are not covered by specific requirements in this document except in 201.11.1.2.2, IEC 60601-1:2005+AMD1:2012+AMD2:2020, 7.2.13 and 8.4.1.
NOTE 2        See also IEC 60601-1:2005+AMD1:2012+AMD2:2020, 4.2.
This document can also be applied to ME equipment and their accessories used for compensation or alleviation of disease, injury, or disability.
This document is not applicable to pulse oximeter equipment intended for use in laboratory research applications nor to oximeters that require a blood sample from the patient.
This document is not applicable to pulse oximeter equipment intended solely for foetal use.
This document is not applicable to remote or slave (secondary) equipment that displays SpO2 values that are located outside of the patient environment.
NOTE 3        ME equipment that provides selection between diagnostic and monitoring functions is expected to meet the appropriate requirements of this document when configured for that function.
This document is applicable to pulse oximeter equipment intended for use under extreme or uncontrolled environmental conditions outside the hospital environment or physician’s office, such as in ambulances and air transport. Additional standards can apply to pulse oximeter equipment for those environments of use.
This document is a particular standard in the IEC 60601-1 and ISO and IEC 80601 series of standards.

This document applies to the basic safety and essential performance of a humidifier, also hereafter referred to as ME equipment, in combination with its accessories, the combination also hereafter referred to as ME system.
This document is also applicable to those accessories intended by their manufacturer to be connected to a humidifier where the characteristics of those accessories can affect the basic safety or essential performance of the humidifier.
EXAMPLE 1           Heated breathing tubes (heated-wire breathing tubes) or ME equipment intended to control these heated breathing tubes (heated breathing tube controllers).
NOTE 2        Heated breathing tubes and their controllers are ME equipment and are subject to the requirements of IEC 60601‑1.
NOTE 3        ISO 5367 specifies other safety and performance requirements for breathing tubes.
This document includes requirements for the different medical uses of humidification, such as invasive ventilation, non-invasive ventilation, nasal high-flow therapy, and obstructive sleep apnoea therapy, as well as humidification therapy for tracheostomy patients.
NOTE 4        A humidifier can be integrated into other equipment. When this is the case, the requirements of the other equipment also apply to the humidifier.
EXAMPLE 2           Heated humidifier incorporated into a critical care ventilator where ISO 80601‑2-12 also applies.
EXAMPLE 3           Heated humidifier incorporated into a homecare ventilator for dependent patients where ISO 80601‑2‑72 also applies.
EXAMPLE 4           Heated humidifier incorporated into sleep apnoea therapy equipment where ISO 80601‑2‑70 also applies.
EXAMPLE 5           Heated humidifier incorporated into ventilatory support equipment where either ISO 80601-2-79 or ISO 80601-2-80 also apply.
EXAMPLE 6           Heated humidifier incorporated into respiratory high-flow therapy equipment where ISO 80601‑2‑90 also applies.
This document also includes requirements for an active HME (heat and moisture exchanger), ME equipment which actively adds heat and moisture to increase the humidity level of the gas delivered from the HME to the patient. This document is not applicable to a passive HME, which returns a portion of the expired moisture and heat of the patient to the respiratory tract during inspiration without adding heat or moisture.
NOTE 5        ISO 9360‑1 and ISO 9360‑2 specify safety and performance requirements for a passive HME.
NOTE 6        If a clause or subclause is specifically intended to be applicable to ME equipment only, or to ME systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME equipment and to ME systems, as relevant.
Hazards inherent in the intended physiological function of ME equipment or ME systems within the scope of this document are not covered by specific requirements in this document except in IEC 60601‑1:2005+AMD1:2012+AMD2:2020, 7.2.13 and 8.4.1.
NOTE 7        Additional information can be found in IEC 60601‑1:2005+AMD1:2012+AMD2:2020, 4.2.
This document does not specify the requirements for cold pass-over or cold bubble-through humidification devices, the requirements for which are given in ISO 20789.
This document is not applicable to equipment commonly referred to as “room humidifiers” or humidifiers used in heating, ventilation and air conditioning systems, or humidifiers incorporated into infant incubators to humidify the chamber

This document specifies both a procedure for preliminary examination of a single sample as received for testing, and a procedure for preparing a test sample by blending and reduction of a series of samples representative of a consignment or a bulk delivery of fluid fertilizer.
NOTE            This document complements the corresponding standard for solid fertilizers (ISO 14820-2).

IEC 61439-8:2026 specifies requirements for the design and verification of low voltage switchgear and controlgear assemblies for use in photovoltaic installations.
PVAs have the following characteristics:
- assemblies used for the combination of electrical energy in DC systems for which the input and output voltage does not exceed 1 500 V DC;
- assemblies supplied from an AC network where the voltage does not exceed 1 000 V AC for auxiliary and control purposes;
- stationary assemblies with an enclosure;
- assemblies intended for operation by authorised persons (see IEC 61439 1:2020, 3.7.17), but can be located in an area accessible to ordinary persons (see IEC 61439 1:2020, 3.7.16);
- suitable for indoor or outdoor installation.
This document identifies definitions, specifies the service conditions, details the construction requirements, defines the technical characteristics, and provides verifications for PVAs. PVAs can also include control or signalling devices, or both, associated with the distribution of electrical energy. This document applies to all PVAs whether they are designed and manufactured on a one-off basis or fully standardized and manufactured in quantity. Either the manufacture or assembly, or both, can be carried out by an entity other than the original manufacturer (see IEC 61439 1:2020, 3.10.1).
This document does not apply to:
- individual devices, for example, circuit-breakers, fuse switches and self-contained components such as, motor starters, switch mode power supplies (SMPS), uninterruptable power supplies (UPS), basic drive modules (BDM), complete drive modules (CDM), adjustable speed power drives systems (PDS), stand-alone energy storage systems (battery and capacitor systems), other electronic equipment which comply with their relevant product standards, such as junction boxes of photovoltaic modules. This document describes their integration into a PVA or an empty enclosure used as a part of a PVA;
- photovoltaic power conversion equipment (PCE) incorporating DC combination sub-systems, covered by the IEC 62109 series.
Some applications, such as either explosive atmospheres or functional safety, or both, can be subject to the requirements of other standards or local installation rules in addition to those specified in the IEC 61439 series. This document does not apply to the specific types of assemblies covered by other parts of the IEC 61439 series.

This document specifies the calculation method, based on Life Cycle Assessment (LCA) and other quantified environmental information, to assess the environmental performance of a building and its site, during whole life cycle, based on a building life cycle model. It also establishes a system for the reporting and communication of the outcome of the assessment.
The document gives:
-   the description of the object of assessment based on the functional equivalent;
-   the system boundary that applies at the building level;
-   calculation rules and procedure to be used to compile and assess the life cycle inventory and life cycle environmental impacts of buildings;
-   the list of indicators and procedures for the calculation of these indicators;
-   demand for information concerning building generated energy reporting;
-   the requirements for the data necessary for the calculation;
-   provides recommendations on how to assess aspects at the local environment level; and
-   the requirements for presentation of the results in reporting and communication.
The approach to the assessment covers all stages of the building life cycle and is based on data obtained from Environmental Product Declarations (EPD) and their "information modules" (EN 15804:2012+A2:2019), generic data according to EN 15941 and other data and information necessary and relevant for carrying out the assessment. The assessment includes all building related construction products, processes and services, used over the life cycle of the building.
The document is applicable to new, existing buildings and buildings undergoing refurbishment or any other kind of activity to extend its service life. Environmental impacts and aspects that are not related to the building are outside the scope of this standard. Methodologies for and approaches to the interpretation and the making of value judgments of the results of the assessment are outside the scope of this document.
The document also provides the methodological basis and assessment rules to support the achievement of environment related macro-objectives in Europe and instruments such as the European reporting framework Level(s).
NOTE   More information on the European reporting framework Level(s)can be found at Level(s) (europa.eu).
Informative Annexes B and C provide non-LCA information covering environmental aspects at the local environment level and additional information on end-of-life scenarios.

This document describes a digital twin system for monitoring and managing the robotic multilayer and multipass gas-shielded metal arc welding process.

This document applies to the basic safety and essential performance of respiratory high-flow therapy equipment, as defined in ‎201.3.262, hereafter also referred to as ME equipment or ME system, in combination with its accessories:
intended for use with patients who can breathe spontaneously; and
intended for patients who would benefit from improved alveolar gas exchange; and who would benefit from receiving high-flow humidified respiratory gases, which can include a patient whose upper airway is bypassed.
EXAMPLE 1 Patients with Type 1 Respiratory Failure who exhibit a reduction in arterial blood oxygenation.
EXAMPLE 2 Patients who would benefit from reduced work of breathing, as needed in Type 2 Respiratory Failure, where arterial carbon dioxide is high.
EXAMPLE 3 Patients requiring humidification to improve mucociliary clearance.
Respiratory high-flow therapy equipment is utilized in both professional healthcare facilities and the home healthcare environment. This standard specifically addresses respiratory high-flow therapy equipment for acute or infant care, predominantly found in hospitals. A separate document for long term high-flow therapy in the home healthcare environment is expected to be forthcoming.
Respiratory high-flow therapy equipment can be:
fully integrated ME equipment; or
a combination of separate items forming a ME system.
This document also applies to other types of respiratory equipment when that equipment includes a respiratory high-flow therapy mode.
NOTE 2  This document and ISO 80601-2-12 are applicable to a critical care ventilator with a high-flow therapy mode.
NOTE 3  This document and ISO 80601-2-72 are applicable to ventilator for ventilator-dependent patients in the home healthcare environment with a high-flow therapy mode.
NOTE 4  This document and ISO 80601-2-13 are applicable to an anaesthetic workstation with a high-flow therapy mode.
Respiratory high-flow therapy equipment can be transit-operable.
This document is also applicable to those accessories intended by their manufacturer to be connected to the respiratory high-flow therapy equipment, where the characteristics of those accessories can affect the basic safety or essential performance of the respiratory high-flow therapy equipment.
EXAMPLE 4         Breathing sets, connectors, humidifier, breathing system filter, external electrical power source, distributed alarm system, high-flow nasal cannula, tracheal tube, tracheostomy tube, face mask and supra-laryngeal airway.
NOTE 5        Accessories are assessed with the relevant clauses of this document when configured as part of respiratory high-flow therapy equipment.
If a clause or subclause is specifically intended to be applicable to ME equipment only, or to ME systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME equipment and to ME systems, as relevant.
Hazards inherent in the intended physiological function of ME equipment or ME systems within the scope of this document are not covered by specific requirements in this document except in the general standard, 7.2.13 and 8.4.1.
NOTE 6        Additional information can be found in the general standard, 4.2.
This document does not specify the requirements for:
ventilators or accessories for ventilator-dependent patients intended for critical care applications, which are given in ISO 80601‑2‑12;
ventilators or accessories intended for anaesthet

This document specifies methods for the enumeration of thermoresistant spores of thermophilic bacteria in heat-processed milk and dried milk products by using a colony-count technique at 55 °C after heating the sample at 106 °C or 100 °C. The applicability of this document is limited to heat-processed milk including pasteurized, ultra-high temperature (UHT) processed and sterilized milk; as well as dried whole milk, skim milk, buttermilk and whey products.

This document defines the term nonwovens and provides auxiliary terminology to distinguish nonwovens from other materials.

This document provides requirements for the evaluation process of any rigid packaging which has its main component, in weight, predominantly made of EPS, with respect to compatibility of the design with recycling processes.
Packaging constituents and packaging components made of other materials than EPS are also covered by this document as they need to be evaluated on compatibility with polymer recycling.
Unless otherwise stated, in the interests of better readability, ‘EPS packaging’ always includes ‘EPS white goods packaging and fish boxes’.

This document covers the design of any rigid packaging with the main body of the packaging unit predominantly made of PE or PP and the design of separate components predominantly made of rigid PE or rigid PP, with respect to compatibility of the design with state-of-the-art collection, sorting and recycling processes and useability of the recyclates in an application.
Packaging constituents and packaging components made of other materials than PE and PP are also covered by this document as they need to be evaluated on compatibility with PE or PP polymer recycling.

This document provides requirements for the evaluation process of any rigid packaging with the main body of the packaging unit predominantly made of PS or XPS and the design of separate components predominantly made of rigid PS or XPS, with respect to compatibility of the design with state-of-the-art collecting, sorting and recycling processes, and the characterization of the output(s) compared to a reference material.
Packaging constituents and packaging components made of other materials than PS and XPS are also covered by this document as they need to be evaluated on compatibility with PS or XPS polymer recycling.

This document specifies requirements for classification of covered electrodes and deposited metal in the as-welded condition and in the post-weld heat-treated condition for manual metal arc welding of high-strength steels with a minimum yield strength greater than 500 MPa or a minimum tensile strength greater than 570 MPa. This document is a combined specification providing a classification utilizing a system based on the yield strength and an average impact energy of 47 J of the all-weld metal, or utilizing a system based on the tensile strength and an average impact energy of 27 J of the all-weld metal. Clauses, subclauses and tables which carry the suffix “System A” are applicable only to covered electrodes classified under the system based on the yield strength and an average impact energy of 47 J of the all-weld metal given in this document. Clauses, subclauses and tables which carry the suffix “System B” are applicable only to covered electrodes classified under the system based on the tensile strength and an average impact energy of 27 J of the all-weld metal given in this document. Subclauses and tables which do not have either the suffix “System A” or the suffix “System B” are applicable to all covered electrodes classified under this document.

This document applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL BEDS as defined in 201.3.214, intended for ADULTS as defined in 201.3.222. Included in the scope are both electrical and non-electrical (manual) MEDICAL BEDS with or without adjustable functions. This document is applicable to either a BED-LIFT or a detachable MATTRESS SUPPORT PLATFORM or both. The combination of BED-LIFT or a detachable MATTRESS SUPPORT PLATFORM with a compatible non-MEDICAL BED as specified by the MANUFACTURER is also considered a MEDICAL BED. This document does not apply to: - MEDICAL BEDS for CHILDREN and ADULTS with atypical anatomies (ADULTS ranging outside the definition for ADULTS in 202.3.222) covered by IEC 80601-2-89; - SPECIALITY MATTRESS covered by ISO 20342 series; - devices for which the INTENDED USE is mainly for examination or transportation under medical supervision (e.g. stretcher, examination table); - all requirements for MEDICAL BEDS with special functionality. If a clause or subclause is specifically intended to be applicable to a MEDICAL BED only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to MEDICAL BED and to ME SYSTEMS, as relevant. HAZARDS inherent in the intended physiological function of MEDICAL BED or ME SYSTEMS within the scope of this document are not covered by specific requirements in this document except in 7.2.13 and 8.4.1 of IEC 60601-1:2005, IEC 60601-1:2005/AMD1:2012 and IEC 60601-1:2005/AMD2:2020.

This document covers the design of any rigid packaging which has its main component, in weight, predominantly made of EPS, with respect to compatibility of the design with state-of-the-art collecting, sorting, and recycling processes and useability of the recyclates in an application.
Packaging constituents and packaging components made of other materials than EPS are also covered by this document as they need to be evaluated on compatibility with polymer recycling.
Unless otherwise stated, in the interests of better readability, ‘EPS packaging’ always includes ‘EPS white goods packaging and fish boxes’.

This document gives guidance on the risk-based approach to follow for the design and operation of the LNG bunker transfer system, including the interface between the LNG bunkering supply facilities and receiving LNG fuelled vessels.
This document provides requirements and recommendations for the development of a bunkering site and facility and the LNG bunker transfer system, providing the minimum functional requirements qualified by a structured risk assessment approach taking into consideration LNG properties and behaviour, simultaneous operations and all parties involved in the operation.
This document is applicable to bunkering of both seagoing and inland trading vessels. It covers LNG bunkering from shore or ship, mobile to ship and ship to ship LNG supply scenarios, as described in Clause 4.

This document specifies requirements and guidelines for:
the design parameters to be provided to the heating, ventilation and air conditioning (HVAC) unit manufacturer by the rolling stock manufacturer (“Customer”) and the railway operator,
the test and inspection items, requirements and methods used by the HVAC unit manufacturer to verify that the HVAC unit conforms with the design parameters.
This document is applicable to HVAC units for the passenger area and driver’s cabs in urban (metro, tramway), suburban, regional and main line vehicles.

This document specifies requirements for high chromium white cast iron grit, as supplied for blast-cleaning processes. It specifies ranges of particle sizes, together with corresponding grade designations. Values are specified for hardness, density, defect/structural requirements, metallographic structure and chemical composition.
The requirements specified in this document apply to abrasives supplied in the new condition only. They do not apply to abrasives either during or after use.
High chromium white cast iron grits are used in both static and site blasting equipment. They are most often selected where there is a possibility for the recovery and re-use of the abrasive.
NOTE 1 Although this document has been developed for preparation of steelwork, these materials are predominantly used for non-ferrous substrates. The properties specified will generally be appropriate for use when preparing other material surfaces, or components, using blast-cleaning techniques, and can be used for applications where no subsequent coating is applied.
NOTE 2 Whenever dissimilar metals are used together, galvanic corrosion can occur.

This document specifies a framework introducing the approaches that can be applied to assess the risks linked to dermal exposure to chemical substances in the workplace. This document provides guidance on the different steps to be taken when performing qualitative and quantitative dermal exposure assessments.
This document is not applicable to inhalation, oral, ocular and mucous membranes exposure, biological agents, wet work and mechanical stressors.

The purpose of this document is to establish the machine-readable (linear, two-dimensional, and composite symbols) and human-readable content for direct marking and labelling of items, parts, and components. This document provides a means for items, parts and components to be marked, and read in either fixtured or hand-held scanning environments at any manufacturer’s facility and then read by customers purchasing items for subsequent manufacturing operations or for final end use. Intended applications include, but are not limited to, supply chain applications, e.g. inventory, distribution, manufacturing, quality control, acquisition, transportation, supply, repair and disposal.

ISO/IEC 30187:2026 specifies the evaluation indicators for IoT systems.
This document is applicable to the compilation of the evaluation indicators for IoT systems in specific industries.
NOTE The indicators identified in this document are typical indicators but are not a comprehensive list; and conversely, not every indicator listed applies to every IoT system.

This document specifies a method for the measurement of flame spread times of vertically oriented textile fabrics and industrial products in the form of single or multi-component textile fabrics (coated, quilted, multilayered, sandwich combinations, and similar combinations) when subjected to a small, defined flame.

This document specifies the requirements for pimento or allspice [Pimenta dioica (L.) Merr.], whole or ground. Recommendations relating to storage and transport conditions are given in Annex A.

This document specifies a test method for the determination of the brittle crack arrest temperature (CAT). This document is applicable to either ferritic or bainitic, or both steel base metals with a body-centred cubic (BCC) crystal lattice structure that exhibit ductile to brittle transition behaviour. The applicable materials are rolled steel plates. This document is intended for steels with a tensile strength of 950 MPa or less and a thickness greater than 6 mm but not exceeding 200 mm. The range of arrest temperatures is between − 196 °C and + 100 °C. This document also specifies the requirements for test method and test procedures when using the isothermal crack arrest test to judge valid test results under isothermal conditions and in order to determine the crack arrest temperature.

This document defines terms relating to sustainable development in communities, smart community infrastructure and related subjects.

This document provides the logical data structure of a mobile Vehicle Certificate (mVC) in conformity with ISO/IEC TS 23220-2 that serves as a confirmation of vehicle register data and confirmation of conformity with issuance requirements. Other documents related to vehicle administration, such as a document that proves ownership of a vehicle and is designed to be used for ownership transfer, are out of scope of this document.

This document: specifies the minimum requirements for the design of labels containing a linear bar code and two dimensional (2D) symbols on product packages to convey data between trading partners; provides guidance for the formatting on the label of data presented in a linear bar code, 2D symbols or human-readable form; provides specific recommendations regarding the choice of linear bar code and 2D symbologies, and specifies quality requirements and classes of bar code density; provides specific recommendations regarding both linear and 2D symbologies, which allow a broad choice for general use of scanning hardware (e.g. area imagers, linear imagers, single line laser scanners, and raster laser scanners); makes recommendations as to label placement, size and the inclusion of free text and any appropriate graphics. This document supports item identification and supply chain processes, at the product package level, such as inventory control, picking, and point of use. NOTE 1 ISO 15394[2] supports the distribution and transportation business processes, so aiding the tracing and tracking of unique shipments. NOTE 2 ISO 28219 addresses the direct part marking. The purpose of this document is to establish the machine readable (e.g. bar code) and human-readable data content of labels applied to product packages. Intended applications include, but are not limited to, inventory, warehouse management, maintenance and point of purchase. While guidance is provided, specific label dimensions or marking areas and the location of the information are not defined in this document. Before implementing this specification, suppliers and manufacturers are advised to review and mutually agree on these details with their trading partners. This document does not supersede or replace any applicable safety or regulatory marking or labelling requirements. It is intended to satisfy the product package requirements of numerous applications and industry groups. As such, it is applicable to a wide range of industries, each of which has specific implementation guidelines. This document is also applicable to any other labelling requirements.

This document specifies the definitions of Zhacai (pickled and squeezed vegetables) and its requirements, including sensory, physical and chemical, contaminants, microorganisms, packaging, labelling, storage and transport. It also describes the corresponding test methods. This document is only applicable to Zhacai.

This document establishes a model-free approach for the isoconversional kinetic analysis of chemical reactions and phase transitions. The isoconversional principle is based on the assumption that the reaction rate at a given conversion depends solely on the temperature, i.e. is independent on the scan rate. This document establishes a method for the determination of the activation energy as a function of the conversion of the reaction or transition. The method is applicable to dynamic and isothermal temperature program measurements done by differential scanning calorimetry (DSC) or thermogravimetry (TG). It can be applicable to other measurement techniques, too, that enable the determination of conversion curves. The method is applicable to the prediction of the kinetic behaviour of reactions and transitions even in temperature regions that are not experimentally accessible. The method is not applicable in the glassy state of polymers.

This document defines the terms used in acoustic emission testing and forms a common basis for standards and general use.

This document specifies a method for the measurement of ease of ignition of vertically oriented textile fabrics and industrial products in the form of single or multi-component textile fabrics (coated, quilted, multilayered, sandwich constructions, and similar combinations), when subjected to a small, defined flame.

This document specifies certain characteristics of the essential oil of rockrose labdanum (Cistus ladanifer L.), with a view to facilitating the assessment of its quality.

This document specifies requirements and gives guidelines for designing accessible software for people with the widest range of physical, sensory and cognitive abilities, including those who are temporarily or situationally disabled, and the elderly. It addresses software considerations for accessibility that complement general design for usability as addressed by parts of the ISO 9241 series, especially ISO 9241-11 and ISO 9241-210.
This document is applicable to the accessibility of interactive systems. It addresses a wide range of software (e.g. home, mobile, office, web, learning support and library systems). It promotes the increased usability of systems for a wider range of users in the widest range of contexts of use.
This document does not apply to the behaviour of, or requirements for, assistive technologies (including assistive software), but it does address the use of assistive technologies as an integrated component of interactive systems.
It is intended for use by those responsible for the specification, design, development, evaluation and procurement of software platforms and software applications.

This document gives the sector specific requirements for the provision of private security services in the energy sector that are additional to the requirements of EN 17483-1.
This document specifies service requirements for quality in organization, processes, personnel and management of a security service provider and/or its independent branches and establishments under commercial law and trade as a provider with regard to security services in the energy sector.
This document defines quality criteria for the delivery of security services in the energy sector requested by public and private clients. This document is suitable for the selection, attribution, awarding and reviewing of the most suitable provider of security services in the energy sector.
NOTE 1 This document is the Part 4 of a series of standards on the provision of private security services for critical infrastructure. See Figure 2.
NOTE 2 It is important that the selection of a private security service provider always represents the best balance between quality and price. This document sets out the minimum requirements that providers are expected to comply with in order for this balance to be struck.
This document is not applicable to private security services in nuclear power plants.
A list of activities for Private Security Companies (PSC) in Critical Infrastructure Protection (CIP) in the energy sector comprises:
1. Perimeter Protection and Surveillance:
-  human - reception services, static guarding, patrols, dog-handler;
- technology – CCTV, unmanned vehicles (air/ground/sea); others;
- operation of a control/monitoring room;
- operation of an alarm monitoring centre;
- access Control and Management (turnstiles, barriers, authorization and badges).
2. Human and technology, e.g. use of screening and detection equipment for:
- vehicles;
- goods;
- visitors;
- staff;
- contractors;
3. Site security and mobile patrolling/ Static guarding activities required to secure a specific facility/area and mobile patrolling on-site and in buildings within the site;
4. Emergency response;
- alarm response;
- first aid response.

This document specifies the quality characteristics of liquid or gaseous hydrogen fuel dispensed at hydrogen refuelling stations for use in proton exchange membrane (PEM) fuel cell vehicle systems, and the corresponding quality assurance considerations for ensuring uniformity of the hydrogen fuel.