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prEN 50463-3:2025 Public enquiry
Comment end date 2026-01-02
Railway applications - Energy measurement on board trains - Part 3: Data handling

EN 50463-3 covers the requirements applicable to the Data Handling System (DHS) of an Energy Measurement System (EMS). EN 50463-3 also includes the basic requirements for the Data Collecting System (DCS) on-ground, relating to the acquisition and storage and export of Compiled Energy Billing Data (CEBD).

EN 62841-4-2:2019/prA2:2025 Public enquiry
Comment end date 2026-01-28
Amendment 2 - Electric motor-operated hand-held tools, transportable tools and lawn and garden machinery - Safety - Part 4-2: Particular requirements for hedge trimmers
prEN ISO 29981 Public enquiry
Comment end date 2026-01-27
Milk products - Enumeration of bifidobacteria - Colony-count technique (ISO 29981:2024)

This document specifies a method for the selective enumeration of bifidobacteria in milk products by using a colony-count technique at 37 °C under anaerobic conditions. The method is applicable to milk products, such as fermented (e.g. yoghurts) and non-fermented milks (e.g. pasteurized milks, skim milks, whey protein concentrates), milk powders and formulae (e.g. infant formulae, follow-up formulae for older infants, products for young children) where these microorganisms are present and viable, in combination with other lactic acid bacteria or alone. The method is also applicable to starter and probiotic cultures. For proposed quality criteria of dairy products, see, for example, CXS 243-2003. Bifidobacteria used in milk products usually belong to the following species (e.g. References [7] and [10]): — Bifidobacterium adolescentis; — B. animalis subsp. animalis; — B. animalis subsp. lactis; — B. bifidum; — B. breve; — B. longum subsp. infantis; — B. longum subsp. longum.

EN 17240:2024/prA1 Public enquiry
Comment end date 2025-12-21
Intelligent transport systems - ESafety - ECall end to end conformance testing for IMS packet switched based systems

This document defines the key actors in the eCall chain of service provision using IMS over packet switched networks (such as LTE/4G) as: 1) In-vehicle system (3.20) (IVS)/vehicle, 2) Mobile network Operator (MNO), 3) Public safety answering point (3.27) (PSAP), and to provide conformance tests for actor groups 1) - 3). NOTE 1 Conformance tests are not appropriate nor required for vehicle occupants (3.36), although they are the recipient of the service. NOTE 2 Third party eCall systems (TPS eCall) are not within the scope of this deliverable. This is because the core TPS-eCall (3.32) standard (EN 16102) does not specify the communications link between the vehicle and the TPS service provider (3.29). NOTE 3 These conformance tests are based an the appropriate conformance tests from EN 16454 which was published before Internet Protocol multimedia Systems (IMS) packet switched networks were available. This deliverable therefore replicates the appropriate tests from EN 16454 (and acknowledge their source); adapt and revise Conformance Test Protocols (CTP) from EN 16454 to an IMS paradigm; or provide new additional tests that are required for the IMS paradigm. Some 14 112-eCall (Pan European eCall) tests provided in EN 16454 are specific to GSM/UMTS circuit switched communications and not appropriate for the IMS paradigm and are therefore excluded from this deliverable. This document therefore provides a suite of ALL conformance tests for IVS equipment, MNO's, and PSAPS, required to ensure and demonstrate compliance to CEN/TS 17184. NOTE 4 Because in the event of non-viability or non-existence of an IMS supporting network at any particular time/location, IMS-eCall systems revert to CS networked eCall systems eCall via GSM/UMTS, IVS and PSAPs need to support, and prove compliance to both IMS and CS switched networks. The Scope covers conformance testing (and approval) of new engineering developments, products and systems, and does not imply testing associated with individual installations in vehicles or locations.

ISO/DIS 20387 Public enquiry
Comment end date 2026-01-05
Biotechnology — Biobanking — General requirements for biobanks

This document specifies general requirements for the competence, impartiality and consistent operation of biobanks including quality control requirements to ensure that collections of biological material and associated data are of appropriate quality. This document is applicable to all organizations performing biobanking. This can include biobanking of biological material: a) from multicellular organisms (e.g. human, animal, fungus and plant); b) from microorganisms; c) derived from sources such as environmental samples (e.g. soil, sediment, water, air). Biobank users, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies, and others can also use this document in confirming or recognizing the competence of biobanks. This document does not apply to biological material intended for therapeutic use. NOTE 1 International, national or regional regulations or requirements can also apply to specific topics covered in this document. NOTE 2 For entities handling human materials procured and used for diagnostic and treatment purposes, ISO 15189 and other clinical standards are intended to apply first and foremost.

prEN IEC 60335-2-6:2025/prAA:2025 Public enquiry
Comment end date 2026-01-28
Household and similar electrical appliances - Safety - Part 2-6: Particular requirements for stationary cooking ranges, hobs, ovens and similar appliances

This European standard deals with the safety of stationary electric cooking appliances, such as cooking ranges, hobs, and ovens, for household use, their rated voltage being not more than 250 V for single-phase appliances connected between one phase and neutral, and 480 V for other appliances including direct current (DC) supplied appliances and battery-operated appliances

ISO/DIS 30439 Public enquiry
Comment end date 2025-12-20
Human Resource Management — Safe Handling of Data

This standard establishes guidelines for organizations in the safe handling of HRM data. This standard pertains to data derived for, from, or used within HRM activities and processes. This standard applies to both for- and non-profit organizations of any size and applies in all sectors and geographies. This standard covers the safe handling of HRM data, in any format, whether collected, maintained, or used by a Human Resources department or an alternative party such as third parties, vendors, or non-HR departments (e.g., Finance, Operations, etc.). This standard concerns only the safe handling of HRM data; characteristics of the HRM data itself such as the quality, reliability, and validity are not within the scope of this standard (See ISO/FDIS 30435:2023 Workforce Data Quality). This standard includes the safe handling of data related to any individual for whom information (regardless of format) is utilized as part of the HRM data life cycle. This may include past and present employees, contractors, directors/board members, applicants, and formerly or indirectly associated individuals. It does not include privacy for customers, suppliers, or other third parties when the data exists outside of HRM (See ISO 27001 and 27002 for data privacy standards non-specific to HRM data and ISO 38505 IT Governance for standards related to data governance in general). In addition to the safe handling recommendations for HRM data included within this standard, other standards may provide additional guidance and actions recommended for the general management and protection of certain types of HRM data. For example, ISO 10667 (Assessment service delivery - Procedures and methods to assess people in work and organizational setting) focuses on the systematic method and procedure for ascertaining or measuring work‑related knowledge, skills, abilities, performance, or other characteristics of an individual or group of individuals provides suggestions for ensuring assessment participants' data protection and appropriate use of personal data.

prEN IEC 60335-2-11:2025 Public enquiry
Comment end date 2026-01-21
Household and similar electrical appliances - Safety - Part 2-11: Particular requirements for tumble dryers

This European Standard deals with the safety of electric tumble dryers intended for household and similar purposes. The rated voltage being not more than 250 V for single-phase appliances and 480 V for other appliances.

prEN IEC 60335-2-111:2025 Public enquiry
Comment end date 2026-01-28
Household and similar electrical appliances - Safety - Part 2-111: Particular requirements for electric ondol mattress with a non-flexible heated part

This European Standard deals with the safety of electric ondol-mattresses for household and similar purposes, their rated voltage being not more than 250 V including direct current (DC) supplied appliances and battery-operated appliances. This standard also applies to control units supplied with the appliance

prEN IEC 63171-1:2025 Public enquiry
Comment end date 2025-12-17
Connectors for electrical and electronic equipment - Part 1: Detail specification for 2-way, shielded or unshielded, free and fixed connectors - Mechanical mating information, pin assignment and additional requirements for Type 1 (copper LC style)

This part of IEC 63171 covers two-way, shielded or unshielded, free and fixed connectors known as Type 1, for balanced single-pair data transmission with frequencies up to 600 MHz and with current carrying capacity up to 2,0 A at 60 °C. It specifies the common dimensions, and provides the mechanical, electrical, signal integrity, and environmental characteristics, the reliability specifications and corresponding tests for these connectors

prEN IEC 62841-3-17:2025/prAA:2025 Public enquiry
Comment end date 2025-12-24
Electric motor-operated hand-held tools, transportable tools and lawn and garden machinery - Safety - Part 3-17: Particular requirements for transportable table masonry saws
prEN 1651 Public enquiry
Comment end date 2026-01-20
Paragliding equipment - Harnesses - Safety requirements and strength tests

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

prEN IEC 60335-2-82:2025/prAA:2025 Public enquiry
Comment end date 2026-01-28
Household and similar electrical appliances - Safety - Part 2-82: Particular requirements for amusement machines and personal service machines

This European standard deals with the safety of electric commercial amusement machines and personal service machines, their rated voltage being not more than 250 V for single-phase appliances and 480 V for other appliances, including direct current (DC) supplied appliances and battery-operated appliances

prEN IEC 62973-3:2025 Public enquiry
Comment end date 2025-12-17
Railway applications - Rolling stock - Batteries for auxiliary power supply systems - Part 3: Lead acid batteries

The part 3 of IEC 62973 shall be transferred to a EN IEC by this NWIP. Later, in a second step, by a further NWIP, common modifications to the EN IEC version will be added. The scope of the original IEC version remains unchanged for the endorsement as EN IEC.

prEN ISO 10318-2 Public enquiry
Comment end date 2025-12-21
Geosynthetics - Part 2: Symbols and pictograms (ISO/DIS 10318-2:2025)

The intent of ISO 10318-2:2015 is to define property symbols, graphical symbols, and pictograms used in EN and ISO geosynthetics standards. Definitions of particular or specific symbols and pictograms terms not included in this this part of ISO 10318 can be found in the International Standards describing appropriate test methods.

EN 62817:2015/prA2:2025 Public enquiry
Comment end date 2026-01-21
Amendment 2 - Photovoltaic systems - Design qualification of solar trackers
prEN ISO 9308-4 Public enquiry
Comment end date 2026-01-27
Water quality - Enumeration of Escherichia coli and coliform bacteria - Part 4: Membrane filtration method for Escherichia coli in water with high levels of background bacteria (ISO/DIS 9308-4:2025)

This document describes a highly specific method for the enumeration of Escherichia coli (E. coli) in water. The method is based on membrane filtration followed by culture at 44 °C on chromogenic agar medium containing an ingredient for the detection of the enzyme β-glucuronidase, and calculation of the number of target organisms in the sample[5,6,13]. Because of the high specificity of the method, this document is suitable for waters with high levels of background bacteria, such as surface waters including bathing water and wastewater provided that they contain little particulate or colloidal matter relative to the E. coli concentration. The method can be used for fresh water and, with an adaptation, for marine water. E. coli strains which do not grow at 44 °C and those that are β-glucuronidase negative, such as E. coli O157, will not be detected as E. coli by this method. This method is not applicable to the enumeration and detection of coliform bacteria other than E. coli.

prEN IEC 63524:2025 Archived
Comment end date 2025-12-10
Artificial Intelligence enabled Medical Devices - Computer assisted analysis software for pulmonary images - Algorithm performance test methods
prEN 18256 Public enquiry
Comment end date 2025-12-16
Digestate - Determination of the residual biogas potential

This document specifies a method for the determination of the residual biogas potential in digestate in an anaerobic environment.

prEN IEC 63440:2025 Public enquiry
Comment end date 2025-12-31
Ultrasonics - Measurement of temperature rise produced by medical ultrasonic equipment
prEN ISO 11616 Public enquiry
Comment end date 2026-01-15
Health informatics - Identification of medicinal products - Data elements and structures for unique identification and exchange of regulated pharmaceutical product information (ISO/DIS 11616:2025)

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

prEN 12896-7 Public enquiry
Comment end date 2026-02-01
Public transport - Reference data model - Part 7: Driver management

1.1 General Scope of the Standard The main objective of the present standard is to present the Reference Data Model for Public Transport, based on: - the Reference Data Model, EN 12896, known as Transmodel V5.1; - EN 28701:2012, Intelligent transport systems - Public transport - Identification of Fixed Objects in Public Transport (IFOPT), although note that this particular standard has been withdrawn as it is now included within Parts 1 and 2 of this European Standard (EN 12896-1:2016 and EN 12896-2:2016) following their successful publication; incorporating the requirements of: - EN 15531-1 to -3 and CEN/TS 15531-4 and -5: Public transport - Service interface for real-time information relating to public transport operations (SIRI); - CEN/TS 16614-1 and -2: Public transport - Network and Timetable Exchange (NeTEx), in particular the specific needs for long distance train operation. Particular attention is drawn to the data model structure and methodology: - the data model is described in a modular form in order to facilitate the understanding and the use of the model; - the data model is entirely described in UML. The following functional domains are considered: - Network Description: routes, lines, journey patterns, timing patterns, service patterns, scheduled stop points and stop places; - Timing Information and Vehicle Scheduling (runtimes, vehicle journeys, day type-related vehicle schedules); - Passenger Information (planned and real-time); - Fare Management (fare structure, sales, validation, control); - Operations Monitoring and Control: operating day-related data, vehicle follow-up, control actions; - Driver Management: - Driver Scheduling (day-type related driver schedules), - Rostering (ordering of driver duties into sequences according to some chosen methods), - Driving Personnel Disposition (assignment of logical drivers to physical drivers and recording of driver performance); - Management Information and Statistics (including data dedicated to service performance indicators). The data modules dedicated to cover most functions of the above domains will be specified. Several concepts are shared by the different functional domains. This data domain is called "Common Concepts". 1.2 Functional Domain Description The different functional domains (enumerated above) taken into account in the present document, and of which the data have been represented as the reference model, are described in EN 12896-1, Public transport - Reference data model - Part 1: Common concepts. 1.3 Particular Scope of this Document The present document entitled Public transport - Reference data model - Part 7: Driver management incorporates the following data packages: - Driver Scheduling; Rostering; - Personnel Disposition; - Driver Control Actions. This document itself is composed of the following parts: - Main document (normative) presenting the data model for the concepts shared by the different domains covered by Transmodel, - Annex A (normative), containing the data dictionary, i.e. the list of all the concepts and attribute tables present in the main document together with the definitions, - Annex B (normative), providing a complement to EN 12896-1:2016, particularly useful for Parts 4 to 8 of the Public Transport Reference Data Model; and - Annex C (informative), indicating the data model evolutions.

prEN ISO 8537 New
Comment end date 2026-02-10
Sterile single-use syringes, with or without needle, for insulin (ISO/DIS 8537:2025)

ISO 8537:2016 specifies requirements and test methods for empty, sterile, single-use syringes, with or without needles, made of plastic materials and intended solely for the injection of insulin, with which the syringes are filled by the end user. This International Standard covers syringes intended for single-use only in humans and with insulins of various concentrations. The insulin syringes specified in this International Standard are intended for use (i.e. insulin injection) immediately after filling and are not intended to contain insulin for extended periods of time. ISO 8537:2016 excludes single-use syringes made of glass, syringes for use with power-driven syringe pumps, syringes that are pre-filled by the manufacturer, and syringes intended to be stored after filling (e.g. in a kit intended for filling by a pharmacist).

prEN ISO 17228 New
Comment end date 2025-12-11
Leather - Tests for colour fastness - Change in colour with accelerated ageing (ISO/DIS 17228:2025)

ISO 17228:2015 specifies various ageing procedures to obtain an indication of the changes that could occur when leather is exposed to a certain environment for a prolonged time. Over time, the surface colour of leather and the leather itself change due to ageing and to the action of the surroundings on the leather. The test conditions to be used depend on the type of leather and its intended use. This procedure can also be used to age specimens for the test of dimensional change according to ISO 17130.

prEN 18213-2 Public enquiry
Comment end date 2025-12-16
District heating and district cooling pipes - Bonded single and twin pipe systems for directly buried hot and cold water networks - Part 2: Qualification testing of PE-Welder

This document specifies the methods of examining the knowledge and skill set of the PE-welder required to carry out on-site joint casing connections on thermally insulated single and twin pipe systems for directly buried hot and cold water networks according to and .The application of these specified methods specifications ensures that the examination is carried out according to a standardised examining procedure. This document applies to the following processes: - preparatory works for joint casing assembly; - assembling and testing the elements for surveillance systems; For special surveillance systems it can be important to have additional training.preparatory works for joint casing system installation; - assembling weldable joint casing system;executing hot gas welding and hot gas extrusion weldingverifying joint tightness (leakage testing); - thermally insulating the joint casing (PUR foaming or half-shell); - sealing fill & vent openings (weldable plugs); - assessing overall installation quality of the completed joint connection (non-destructive).

Total records found: 271
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