CEN - European Committee for Standardization

This document specifies the required characteristics of a light weight coaxial cable, 50 Ω, type KX for use in aircraft electrical systems at operating temperature between −55 °C and 200 °C and specially for high frequency up to 6 GHz. Nevertheless, if needed, −65 °C is also acceptable as shown by rapid change of temperature test.

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.

This document covers the design of any rigid PET packaging that does not fall within the definition of a PET bottle as outlined in Part 4 of this document, with respect to compatibility of the design with the state-of-the-art collection, sorting and recycling processes and useability of the recyclates in an application.
Packaging constituents and packaging components made of materials other than PET are also covered by this document as they need to be evaluated on compatibility with PET polymer recycling.

This Technical Specification (TS) series provide a generic framework for the establishment of requirements and their evaluation methodology for biometric products. The requirements depend on the biometric mode considered, and are adapted to each scenario, through the definition of a variety of application profiles (APs). In addition, this TS series provides the definition of the individual tests that can be applied to a biometric product.
This document specifies the context for the evaluation of biometric products within the context of the European Union, as well as the general requirements for such evaluation. This will be defined in a biometric mode-independent point of view, as well as not being biased by the particular application which is the target of the biometric product to be assessed.
This first part defines the following items:
-   biometric evaluation process;
-   biometric evaluation phases;
-   how to define each particular biometric test;
-   how to define the profiling for a particular application.
NOTE 1   Future parts of the CEN/TS series are planned to address the specifics of each biometric mode. For each of these modalities, this document specifies application-independent tests, as well as a set of APs, that detail the applicable tests, the evaluation parameters, and the passing criteria.
NOTE 2   Regarding biometrics for public sector applications, see also BSI TR 03121 [7] which can apply.
NOTE 3   For an overview of sectors addressed in the Cybersecurity Act, see Regulation (EU) 2019/881.

This document specifies the fuel quality classes and specifications of graded firewood. This document applies only to firewood produced from the following raw materials (see ISO 17225-1:2021, Table 1):
1.1.1 Whole trees without roots;
1.1.3 Stemwood;
1.1.4 Logging residues (thick branches, tops, etc.);
1.2.1 Chemically untreated by-products

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 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 covers the design of any flexible packaging with the main body of the packaging unit predominantly made of PE or PP and the design of separate components predominantly made of flexible PE or flexible PP, with respect to compatibility of the design with state-of-the-art collection, sorting and recycling processes and useability of the recyclates.
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 specifies the requirements relating to:
Steel GX5CrNiCuNb16-4 (1.4525)
Homogenized
Solution treated and precipitation hardened
Investment casting
De ≤ 50 mm
Rm ≥ 900 MPa
for aerospace applications.
ASD-STAN designation FE-CM3801
Material number 1.4525

This document provides a framework and principles for design for recycling documents for assessing the identification of the level of compatibility of plastic-packaging feature with the applicable collection, sorting and recycling processes, describing the level of compatibility.
This document covers any packaging predominantly made of plastic and separate components predominantly made of plastic. It aims to provide a consistent approach for the guidelines and protocols for each polymer and format.

This document describes the transaction information requirements of the transactions used in the collaborations described in EN 17016-1:2024. For each transaction are specified the transaction business requirements, the transaction information data model containing definitions of terms, usage descriptions and cardinality of the information elements and the transaction business rules.
This document describes the following transactions:
1)   Order;
2)   Order Change;
3)   Order Cancellation;
4)   Order Response Simple
5)   Order Confirmation;
6)   Order Rejection;
7)   Order Response;
8)   Order Change Confirmation;
9)   Order Change Rejection;
10)   Order Cancellation Confirmation;
11)   Order Cancellation Rejection;
12)   Order Agreement.
How to claim compliance to a transaction is specified in Clause 6.
How to claim conformance to a transaction is also specified in Clause 6.

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 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 specifies the characteristics of general-purpose eddy current instruments and provides methods for their evaluation and verification.
This document can be completed by an application document specifying acceptance criteria for the characteristics of the eddy current instrument.
Where accessories are used, these are characterized using the principles of this document (e.g. additional external amplifiers).

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 gives guidance on the procedure for the bioaccumulation of substances liable to cause atmospheric pollution. This is done by using the grass species Lolium multiflorum ssp. italicum designated hereafter as Italian rye-grass. It is an active biomonitoring approach insofar as the plants used are first cultivated in set conditions before being exposed at the monitoring locations in the field. The plants then record any pollution events that occur while they are being exposed, allowing such events to be accurately dated.
The document specifies a method for identification and localization of one or more single pollution sources and the tracking of their "plume" on a local or regional scale. The method described also offers a tool to monitor sites in the long term by the repeated application of a clearly defined procedure and to describe the local or regional air pollution situation.
The method described in this document is applicable to solid and gaseous substances deposited on plants, where they can accumulate on their surface or in their tissues. These substances include sulphur, chloride, fluoride and especially metals as well as low volatile organic and halo-organic compounds such as polycyclic aromatic hydrocarbons (PAH), polychlorinated biphenyls (PCB), polybrominated diphenyl ethers (PBDE), polychlorinated dibenzo dioxins (PCDD) and polychlorinated dibenzo furans (PCDF). It is as well possible to verify pesticides which are used in plant protection products. The range of potential substances can be expanded according to the task at hand and the capabilities of conducting trace analyses and assessment.
The method described in this document allows spatial and temporal comparisons and allows for screening, thus providing a first indication of risk. The results of grass culture studies can suggest risks to biota (e.g. via the food chain) which require further investigation.
The method described in this document does not replace physico-chemical methods of direct measurement or modelling of air pollutants and cannot be replaced by them for its part; it complements them by indicating biological effects.
Potential areas of deployment are:
-   permit procedures related to air pollution legislation;
-   preservation of evidence related to the code for protection from pollution;
-   monitoring of emission sources and performance control;
-   assessment of local-scale emission transport;
-   evidence of causation, e.g. related to environmental liability;
-   air quality maintenance plans/strategies;
-   long-term monitoring of ecological effects of atmospheric depositions;
-   detection and assessment of local, regional, and countrywide effects of atmospheric depositions;
-   assessment of risks for humans and/or animals via the food chain.
This document is of interest to those involved in environmental monitoring.

This document specifies the required characteristics of a light weight coaxial cable, 50 Ω, type KW for use in aircraft electrical systems at operating temperature between −55 °C and 180 °C and specially for high frequency up to 6 GHz. Nevertheless, if needed, −65 °C is also acceptable as shown by rapid change of temperature test.

The CEN/TS 18212 series specifies a generic framework for the establishment of requirements and their evaluation methodology for biometric products. The requirements depend on the biometric mode considered, and are adapted to each scenario, through the definition of a variety of application profiles (APs).
This series of standards are expected to provide the evaluation methodology, the individual tests, and the APs (with their particular requirements).
This document specifies:
-   tests for evaluating the interoperability of all biometric input data (received or read);
-   test for evaluating the interoperability of all biometric output data (stored or transmitted);
-   test for evaluating the interoperability of all exchange of information between the TOE and external components or devices.
NOTE 1   Additional parts are provided covering the specifics of each biometric mode. For each of these modalities, application-independent tests are defined, as well as a set of APs, that detail the applicable tests, the evaluation parameters, and the passing criteria.
The Technical Specifications within this series can be taken by any certification body and/or sector, to define and evaluate the requirements for their biometric products within their selected applications.
NOTE 2   Regarding biometrics for public sector applications, see also BSI TR 03121 [2] which can apply.
NOTE 3   For an overview of sectors addressed in the Cybersecurity Act, see Regulation (EU) 2019/881.
NOTE 4   This part defines all potential tests that could be applicable when evaluating the interoperability of a biometric product. It will be the relevant AP, the one that will specify which of these tests are applicable.

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 specifies the requirements for an environmental management system that an organization can use to enhance its environmental performance. It is intended for use by an organization seeking to manage its environmental responsibilities in a systematic manner that contributes to the environmental pillar of sustainability.
This document helps an organization to achieve the intended outcomes of its environmental management system, which provide value for the environment, the organization itself and interested parties. The intended outcomes of an environmental management system include:
enhancing environmental performance;
meeting compliance obligations;
achieving environmental objectives.
This document is applicable to any organization, regardless of size, type or nature, and applies to the environmental aspects of its activities, products and services that the organization determines it can either control or influence considering a life cycle perspective. This document does not state specific environmental performance criteria.
This document can be used in whole or in part to systematically improve environmental management. Claims of conformity to this document, however, are not acceptable unless all its requirements are incorporated into an organization’s environmental management system and fulfilled without exclusion.

This document provides testing procedures and requirements on the evaluation processes for the sortability of plastic packaging with regard to compatibility of the design with state-of-the-art collecting and sorting processes for the plastic used.
This document covers any packaging predominantly made of plastic and separate packaging components predominantly made of plastic, both in case they undergo sorting processes.

This document specifies a process for a medical laboratory to identify and manage the risks to patients, laboratory workers and service providers that are associated with medical laboratory examinations. The process includes identifying, estimating, evaluating, controlling and monitoring the risks.
The requirements of this document are applicable to all aspects of the examinations and services of a medical laboratory, including the pre-examination, examination, and post-examination aspects including accurate transmission of examination results into the electronic medical record, as well as other technical and management processes described in ISO 15189.
This document does not specify acceptable levels of risk.
This document does not apply to risks from post-examination clinical decisions made by healthcare providers.
This document complements the management of risks affecting medical laboratory enterprises that are addressed by ISO 31000, such as business, economic, legal, and regulatory risks.

This document covers the design of any bottle with the main body of the packaging unit predominantly made of PET and the design of separate components predominantly made of PET, 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 PET are also covered by this document as they need to be evaluated on compatibility with PET polymer recycling.

This standard provides a comprehensive set of procedures for verifying the correct implementation of each capability claimed on a BACnet PICS including:
support of each claimed BACnet service, either as an initiator, executor, or both,
support of each claimed BACnet object-type, including both required properties and each claimed optional property,
(support of the BACnet network layer protocol,
support of each claimed data link option, and
support of all claimed special functionality.

This document provides requirements for the evaluation process of any rigid PET packaging that does not fall within the definition of a PET bottle as outlined in Part 4 of this document, with respect to compatibility of the design with state-of-the-art collection, 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 PET are also covered by this document as they need to be evaluated on compatibility with PET polymer recycling.

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 specifies the characteristics of grooved pins with one-third-length centre oval grooves (with closed ends), in steel and stainless steel, and with a nominal diameter from 1 mm to 25 mm.
These grooved pins are designed to fulfil the main following functions:
relative rotation of the assembled parts, and
positioning or guiding,
with an easy installation (due to its symmetrical shape) and a medium level of pull-out resistance (due to the elastic fit behaviour of the pin).
The general requirements (including functional principles for grooved pins and assembly) are specified in ISO 13669.

This document specifies concepts used in the field of cloud computing. These concepts expand upon the cloud computing vocabulary defined in ISO/IEC 22123-1 and provide a foundation for other documents that are associated with cloud computing.

ISO/IEC 22123-1:2023 defines terms used in the field of cloud computing.

This document specifies a test method and the minimum requirements for bactericidal and yeasticidal and/or fungicidal and/or tuberculocidal and/or mycobactericidal activity of chemical disinfectant products that form a homogeneous, physically stable preparation when diluted with hard water - or in the case of ready-to-use products - with water.
This document is applicable to products that are used in the medical area for disinfecting non-porous surfaces including surfaces of medical devices by wiping or mopping - regardless if they are covered by the Medical Device Regulation [7] or not.
Due to the new methods of application of surface disinfectants like pre-impregnated wipes this document was established to cover the different application methods.
FprEN 16615 is applicable for four methods of application of products for wiping and/or mopping:
a)   soaking any non-specified wipe or mop with product;
b)   spraying the product on any non-specified wipe and / or mop or a specified wipe or mop;
c)   impregnation of specified wipes or mops by the user with the product according to the manufacturer’s recommendation;
d)   pre-impregnation of specified wipes or mop by the manufacturer as ready-to-use wipes or mops.
In all types of application, the water control is done with the standard wipe (5.3.2.17.1), because it is a process or method control.
This document does not apply to products that are sprayed on or flooding surfaces, without wiping in the contact time. In this case, the methods of phase 2/ stage 2 without mechanical action apply.
The test-surface (5.3.2.16) was selected as standard surface to cover all non-porous surfaces. This document does not apply to the testing of the influence of different surfaces.
This document is applicable to areas and situations where disinfection is medically indicated. Such indications occur in patient care, for example:
-   in hospitals, in community medical facilities and in dental institutions;
-   in clinics of schools, of kindergartens and of nursing homes;
and can occur in the workplace and in the home. It can also include services such as laundries and kitchens supplying products directly for the patients.
NOTE   This method corresponds to a phase 2, step 2 test.
EN 14885 specifies in detail the relationship of the various tests to one another and to “use recommendations”.

This document specifies a procedure for the determination of the dimensional changes and distortion out of plane likely to take place when textile floor coverings and tiles are subjected to varied water and heat conditions.
The method is applicable to all textile floor coverings and textile floor coverings in tile form.

This document describes a standardized methodology and framework for the development and representation of an ontology that supports a global, open-source approach to implementing the ISO standards on the identification of medicinal products (IDMP) (ISO 11615, ISO/TS 20443, ISO/TS 20451, ISO 11238; ISO/TS 19844, ISO 11239, ISO/TS 20440, and ISO 11240). Realization of the full potential of IDMP requires fully self-describing data. For this purpose, this document describes a methodology and framework that complements the existing conceptual and logical models in the ISO documents on IDMP with an IDMP ontology that enables deep, semantic interoperability based on findable, accessible, interoperable and reusable (FAIR) data principles. This methodology and framework enhance the usage of the IDMP data model as the foundation of medicinal product identification and will ultimately enable collaboration towards drug safety and overall operational efficiency.
This document also describes a methodology for the agile adaptation of the ISO documents on IDMP in connection with cross-jurisdictional IDMP-related legislation and initiatives. This document is intended to be complementary to and independent from formal regulatory guidance. Thus, it enables cross-jurisdictional consistency and supports stakeholders in their regional implementations of IDMP standards. This document does not mandate any specific ontology as an implementation tool, nor is it an instructional guideline on how to build ontologies, which is out of scope of this document.
This document includes key use cases described in the ISO documents on IDMP ISO 11615, ISO 11238 and ISO/TS 19844, as well as further use cases arising from the comprehensive deployment of the ISO documents on IDMP via an ontological framework. Thus, an ontology that represents the IDMP standards aims to cover the complete collection of ISO standards on IDMP regarding key interoperability issues that implementing stakeholders are facing.

This document specifies quality requirements for the chart, test procedure and acceptance level for near, far, and colour vision acuity of NDT personnel. Information for grey scale perception and low contrast can be found in the annexes. This document also specifies the qualification requirements for personnel permitted to carry out the test.
This document is only applicable to vision acuity under defined conditions similar to those encountered during routine NDT inspection. This document does not address an individual’s overall visual acuity and users are advised to consider the need for a general eye examination by specialist medical personnel to ensure general vision acuity.

NOTE 1        There is guidance or rationale for this Clause in A.2.1.
This document specifies the requirements for information supplied by the manufacturer for a medical device or an accessory, as defined in 3.1. This document includes the generally applicable requirements for identification and labels on a medical device or accessory, the packaging, marking of a medical device or accessory, and accompanying information. This document does not specify the means by which the information is to be supplied.
NOTE 2        Some authorities having jurisdiction impose different requirements for the identification, marking and documentation of a medical device or accessory.
Specific requirements of medical device product standards or group standards take precedence over requirements of this document.

This document specifies the cloud computing reference architecture (CCRA).

This document provides general product category rules (PCR) for Type III environmental declarations for wood and wood-based products, including wood-based panels, for use in construction and related construction and in-service processes.
This document complements the core rules for the product category of construction products as defined in EN 15804 and is intended to be used in conjunction with EN 15804.
This document does not cover the assessment of social and economic performances at product level.
The core PCR:
—   define the parameters to be declared and the way in which they are collated and reported;
—   describe which stages of a product’s life cycle are considered in the EPD and which processes are to be included in the life cycle stages;
—   define rules for the development of scenarios;
—   include the rules for calculating the life cycle inventory and the life cycle impact assessment underlying the EPD, including the specification of the data quality to be applied;
—   include the rules for reporting predetermined, environmental and health information, that is not covered by LCA for a product, construction process and construction service where necessary;
—   define the conditions under which construction products can be compared based on the information provided by EPD.
For the EPD of construction services, the same rules and requirements apply as for the EPD of construction products.
Additionally, to the common parts of EN 15804, this document for wood and wood-based products:
—   defines the system boundaries;
—   defines the rules for modelling and assessment of material-specific characteristics such as carbon content and net calorific value of wood;
—   defines allocation procedures for multi-output processes along the wood chain;
—   defines allocation procedures for reuse, recycling and energy recovery;
—   includes the rules for calculating the life cycle inventory and the life cycle impact assessment underlying the EPD, including the assessment of carbon and net calorific value of wood;
—   provides guidance/specific rules for the determination of the reference service life (RSL).

This document specifies a general method of test for determining the oil absorption value of a sample of pigment or extender. The oil absorption value is usually required to be compared with the value determined at the same time on an agreed sample of the product.

This document specifies requirements and test methods for durability, strength, security and functionality of sliding closing devices (SCDs) for windows and door height windows.
This document does not specifically cover the handles used in handle-operated SCDs or the sash fasteners used in cam-operated SCDs, requirements and test methods for which are given in EN 13126 2, EN 13126 3 and EN 13126 14, respectively.
The performance tests incorporated in this document are considered to be reproducible and as such will provide a consistent and objective assessment of the performance of these products throughout CEN Member States.

This document specifies a method [1] for the quantitative determination of saxitoxin (STX), decarbamoyl saxitoxin (dcSTX), neosaxitoxin (NEO), decarbamoyl neosaxitoxin (dcNEO), gonyautoxin 1 and 4 (GTX1,4; sum of isomers), gonyautoxin 2 and 3 (GTX2,3; sum of isomers), gonyautoxin 5 (GTX5), gonyautoxin 6 (GTX6), decarbamoyl gonyautoxin 2 and 3 (dcGTX2,3; sum of isomers), N-sulfocarbamoyl gonyautoxin 2 and 3 (C1,2; sum of isomers) and N-sulfocarbamoyl gonyautoxin 1 and 4 (C3,4; sum of isomers) in (raw) mussels, oysters, scallops and clams. Laboratory experience has shown that this document can also be applied to other marine invertebrates [2], [3] and processed products of those species, however, no complete interlaboratory validation study according to ISO 5725-2 [21] has been carried out so far. The method described was validated in an interlaboratory study [4], [5] and was also verified in a European Union Reference Laboratory for Marine Biotoxins (EURLMB)-performance test aiming the total toxicity of the samples [6]. Toxins which were not available in the first interlaboratory study [4], [5] as dcGTX2,3 and dcNEO were validated in two additional interlaboratory studies [7], [8]. The lowest validated levels [4], [5], [8], are given as mass fraction of toxin (free base) in µg/kg shellfish tissue and also as µmol/kg shellfish tissue and are listed in Table 1.
[Table 1 - Lowest validated levels]
A quantitative determination of GTX6 was not included in the first interlaboratory study but several laboratories detected this toxin directly after solid phase extraction with ion-exchange (SPE-COOH) clean-up and reported a mass fraction (free base) of 30 µg/kg or higher in certain samples. For that reason, the present method is applicable to quantify GTX6 directly, depending on the availability of the standard substance. Whenever GTX6 standard is not commercially available, it is possible to determine GTX6 after hydrolysis of Fraction 2 of the SPE-COOH clean-up, described in 7.4, as NEO. The indirect quantification of GTX6 was validated in two additional interlaboratory studies [7], [8]. A study to compare direct and indirect GTX6 quantification was conducted at the EURLMB [16].
A quantitative determination of C3,4 was included in the first interlaboratory study. The present method is applicable to quantify C3,4 directly, depending on the availability of the standard substance. If no standard substances are available, C3,4 can only be quantified as GTX1,4 if the same hydrolysis protocol used for GTX6 (7.4) is applied to Fraction 1 of the SPE-COOH clean-up [10]. A study to compare direct and indirect C3,4 quantification was conducted at the EURLMB [16].

This document describes a test method for the determination of the flash point of chemicals, lube oils, fuels including aviation turbine fuel, diesel fuel, diesel/biodiesel blends and related products. The precision of this method has been determined over the range of 24,5 °C to 229,5 °C.
NOTE            Apparatus can determine the flash point at higher or lower temperatures than the precision range, however the precision has not been determined.

This document is applicable to flushing valves for WCs and valves for urinals, with automatic hydraulic closure, intended for:
—   WC pans EN 997;
—   single flush urinals EN 13407;
—   siphon acting urinals EN 13407.
It does not apply to no-contact detection valves.
It is intended to specify:
—   marking and identification, physico-chemical, dimensional, leaktightness, pressure behaviour, hydraulic, mechanical endurance and acoustic characteristics of flushing valves for WCs and urinals with automatic closure;
—   test methods used to verify these characteristics;
—   and to determine requirements for the atmospheric interrupter which shall be an integral part of the WC flushing valve.
It is applicable in the following pressure and temperature conditions (see Table 1):
[Table 1 — Conditions of use for tapware]
NOTE   Although this document limits the pressure for WC DN25 and WC DN32 valves till 0,25 MPa (2,5 bar), some European countries have legislation and recommendations for higher pressures.
Health and quality requirements in accordance to European and national legislation for final materials in contact with water intended for human consumption are not covered by this document.

This document specifies a gradient column method for the determination of the density of non-cellular moulded or extruded plastics or pellets in void-free form.

This document gives guidance on the use of regrinds and recycled materials for thermoplastic parts for aerospace use.
This document does not apply to reinforced thermoplastic materials, such as short fibre-reinforced plastics, due to their distinct processing characteristics, material degradation concerns, and stringent aerospace performance requirements.
The intended manufacturing processes for these virgin/regrind blends include standard thermoplastic methods such as injection moulding, extrusion, and blow moulding, among others as appropriate to the application.

Building on the consolidated definitions of NbS, this document establishes a terminology to support the development of an agreed vocabulary, forming the basis of the standardisation process.

This document specifies general construction, performance and material requirements for PN 10 thermostatic mixing valves (TMV) and includes test methods for the verification of mixed water temperature performance at the point of use below 45 °C. This does not exclude the selection of higher temperatures where available. When these devices are used to provide anti-scald protection for children, elderly and disabled persons the mixed water temperature shall be set at a suitable temperature (body temperature - 38 °C). In particular children are at risk to scalding at lower temperatures than adults. This does not obviate the need for supervision of young children.
It applies to valves intended for use on sanitary appliances in kitchens, washrooms (incl. all rooms with sanitary tapware, e.g. toilet and cloakrooms) and bathrooms operating under the conditions specified in Table 1.
This document allows TMVs to supply a single outlet or a small number of outlets in a “domestic” application (e.g. one valve, controlling a shower, bath, basin and/or, bidet), excluding valves specifically designed for supplying a large number of outlets (i.e. for institutional use).
The tests described are type tests (laboratory tests) and not quality control tests carried out during manufacture.
Table 1 - Conditions of use

This document provides requirements on identification and labelling of medicinal products from the point of manufacturing of packaged medicinal product to the point of dispensing the product.
This document outlines commonly accepted international practices for automatic identification and data capture (AIDC) barcoding solutions for applications and applies to manufacturers, distributors, healthcare facilities and all parties involved in labelling and distribution of packaged medicinal products. These users can, however, consider the coding interoperability requirements for other AIDC technologies, e.g. radio frequency identification (RFID); that technology is not addressed in this document except as for information.

This document specifies requirements for the selection, installation, validation, and operation of continuous measuring devices CMDs as follows:
1)   Selection: defining the user requirements, the purposes of the required measurements, associated data quality requirements, and choice of CMDs.
2)   Installation: verifying a complete and correct delivery of the procured CMD and verifying a correctly functioning on-site installation, operation and communication of the CMD.
3)   Validation: verifying that the correctly installed CMD meets all of the original defined user requirements.
4)   Operation: implementing operating and maintenance procedures, processing of data and document traceability.
The overall objective is to obtain representative and reliable measurements when using CMDs to monitor water quality.
This document is applicable to CMDs for monitoring physical and chemical parameters in different types of water.

This document specifies a test method for estimating the transfer of mineral oil saturated hydrocarbons (MOSH) and mineral oil aromatic hydrocarbons (MOAH) from food contact materials containing recycled pulp.
This test method is applicable for examining the extent of migration from paper and board equipped with a barrier or other technical solutions to reduce the amount of migration.
This test method is also applicable to paper and board made from virgin fibres.