Standartų projektų sąrašas

prEN ISO 463 Viešoji apklausa

Komentavimo iki data 2026-03-03

Geometrinės gaminio specifikacijos (GPS). Matmenų matavimo įtaisai. Indikatorių projektinės ir metrologinės charakteristikos (ISO/DIS 463:2025)

ISO 463:2006 specifies the most important design and metrological characteristics of mechanical dial gauges.

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prEN IEC 60953-1:2025 Viešoji apklausa

Komentavimo iki data 2026-01-14

Garo turbinų priimamųjų šiluminių bandymų taisyklės. 1 dalis. Tikslusis didelių kondensacinių garo turbinų bandymo metodas

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prEN IEC 60068-2-64:2025 Viešoji apklausa

Komentavimo iki data 2026-01-30

Aplinkos poveikio bandymai. 2-64 dalis. Bandymai. Fh bandymas. Plačiajuostė atsitiktinė vibracija ir nurodyma

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prEN 13796-1 Viešoji apklausa

Komentavimo iki data 2026-01-29

Lynų kelio įrenginių, suprojektuotų žmonėms vežti, saugos reikalavimai. Vežtuvai. 1 dalis. Griebtuvai, važiuoklės, vidiniai stabdžiai, kabinos, krėslai, vagonėliai, techninės priežiūros vežtuvai, vilktuvai

This European Standard specifies the safety requirements applicable to carriers for cableway installations designed to carry persons. It is applicable to the various types of installations and takes into account their environment. It includes requirements relating to the prevention of accidents and the protection of workers. It does not apply to installations for the transportation of goods or to inclined lifts.

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prEN ISO 18969 Viešoji apklausa

Komentavimo iki data 2026-02-24

Klinikinis medicinos priemonių įvertinimas (ISO/DIS 18969:2025)

This document specifies terminology, principles and a process for the clinical evaluation of medical devices. The process described in this document aims to assist manufacturers of medical devices to estimate the clinical risks associated with a medical device and evaluate the acceptability of those risks in the light of the clinical benefits achieved when the device is used as intended. The requirements of this document are applicable throughout the life cycle of a medical device. The process described in this document applies to the assessment of risks and benefits from clinical data obtained from the use of medical devices in humans. This document specifies general requirements intended to — verify the safety of medical devices when used in accordance with their instructions for use; — verify that the clinical performance or effectiveness of a medical device meet the claims of the manufacturer in relation to its intended use; — verify that there is sufficient clinical evidence to demonstrate the achievement of a positive benefit/risk balance when a medical device is used in the intended patient population in accordance with its intended use; — ensure the scientific conduct of a clinical evaluation and the credibility of conclusions drawn on the safety and performance of a medical device; — define the responsibilities of the manufacturer and those conducting or contributing to a clinical evaluation; and — assist manufacturers, clinicians, regulatory authorities and other bodies involved in the conformity assessment of medical devices. Note 1 This standard can be used for regulatory purposes. Note 2 This document does not apply to in vitro diagnostic medical devices. However, there may be situations, dependent on the device and national or regional requirements, where sections and/or requirements of this document might be applicable.

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prEN ISO/ASTM 52961 Viešoji apklausa

Komentavimo iki data 2026-03-03

Adityvioji gamyba naudojant polimerus. Aplinka, sveikata ir sauga. Bendrieji polimerų naudojimo atliekant medžiagų ekstruziją principai (ISO/ASTM DIS 52961:2025)

This document provides guidance and requirements for risk assessment and implementation of prevention and protection measures relating to material extrusion-based additive manufacturing with polymer materials. The risks covered by this document concern all sub-processes composing the manufacturing process, including the management of waste. This document does not specify requirements for the design of machinery and equipment used for additive manufacturing.

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prEN 15383 Viešoji apklausa

Komentavimo iki data 2026-02-17

Nuotakyno plastikinių vamzdžių sistemos. Termoreaktyvieji stiklo plastikai poliesterinių dervų pagrindu. Šuliniai ir apžiūros šulinėliai

This document applies to: a) manholes, when made from glass-reinforced thermosetting plastics (GRP) based on polyester resin (UP); b) inspection chambers, when made from glass-reinforced thermosetting plastics (GRP) based on polyester resin (UP) which are intended to be used with inverts which are at a depth not exceeding 2 m. These products are intended to be used within a drain or sewer system operating without pressure or occasionally at a head of pressure up to 1 bar. It applies to products, and their joints, intended for use in buried installations and to be installed by open-trench techniques. The units have a circular shape with nominal sizes as specified in EN ISO 23856. The intended use of these products is to provide access to, buried drain or sewer systems for the conveyance of waste water at temperatures up to 50 °C, without pressure or occasionally at a head of pressure up to 1 bar, outside buildings and installed in areas subjected to vehicle and/or pedestrian traffic. It specifies definitions including symbols, requirements and characteristics of manholes, inspection chambers, joints, materials, test methods and marking. NOTE It is the responsibility of the purchaser or specifier to make the appropriate selections, taking into account their particular requirements and any relevant national regulations and installation practices or codes.

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prEN IEC 63466-2:2025 Archyvuotas

Komentavimo iki data 2025-12-31

Plyšiniai bangolaidžiai. 2 dalis. Elipsinių plyšinių bangolaidžių atskiroji specifikacija

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prEN 3475-203 Viešoji apklausa

Komentavimo iki data 2026-01-29

Orlaiviai ir erdvėlaiviai. Orlaiviuose naudojami elektros kabeliai. Bandymo metodai. 203 dalis. Matmenys

This document specifies a method of measuring the dimensions of conductors and cables. It is used together with EN 3475-100.

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prEN IEC 60115-8-10:2025 Viešoji apklausa

Komentavimo iki data 2026-02-06

Pastovieji varžai, naudojami elektroninėje įrangoje. 8-10 dalis. Lentelinė detalioji specifikacija. Spausdintinių plokščių paviršiuje montuojami mažos galios sluoksniniai varžai, priskiriami klasifikaciniam G lygiui ir skirti bendrosios paskirties elektroninei įrangai

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prEN ISO 14001 Viešoji apklausa

Komentavimo iki data 2026-02-19

Aplinkos apsaugos vadybos sistemos. Reikalavimai ir naudojimo gairės (ISO/FDIS 14001:2026)

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 and 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.

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prEN 301 843-8 V1.0.0 (2025-12) Viešoji apklausa

Komentavimo iki data 2026-03-08

Jūrinės radijo ryšio įrangos ir paslaugų elektromagnetinio suderinamumo (EMS) standartas. Elektromagnetinio suderinamumo darnusis standartas. 8 dalis. Radijo švyturių ir vietos nustatymo įtaisų specialiosios sąlygos

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prEN 50463-5:2025 Archyvuotas

Komentavimo iki data 2026-01-02

Geležinkelio taikmenys. Energijos matavimas traukiniuose. 5 dalis. Atitikties vertinimas

EN 50463-5 specifies the conformity assessment arrangements for newly manufactured EMS installed on a traction unit. This includes the integration conformity assessment and installation conformity assessment. In addition, EN 50463-5 also specifies the conformity assessment procedures for device and ancillary component replacement (e.g. due to damage in service), and periodic check to verify the EMS conformity assessment remains valid.

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prEN 489-2 Viešoji apklausa

Komentavimo iki data 2026-01-13

Centralizuoto šilumos tiekimo vamzdžiai. Gamyklinės lanksčiųjų vamzdžių sistemos. Jungčių apvalkalų sistemos

This document specifies requirements and test methods for joint casing systems for factory made flexible pipe systems with a plastic service pipe in accordance with standard series EN 15632 1 to -3, EN 17878 1 to -3 or EN 17414 1 to -3, as applicable. Requirements of joint casing systems for EN 15632-4 are not covered by this document, but by EN 489 1.

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prEN 12896-7 Viešoji apklausa

Komentavimo iki data 2026-02-01

Viešasis transportas. Pamatinių duomenų modelis. 7 dalis. Vairuotojų darbo valdymas

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.

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prEN ISO 8537 Viešoji apklausa

Komentavimo iki data 2026-02-10

Vienkartiniai sterilūs insulino švirkštai su adatomis arba be jų (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).

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prEN ISO 16440 Viešoji apklausa

Komentavimo iki data 2026-02-26

Naftos ir gamtinių dujų pramonė. Transportavimo vamzdynais sistemos. Vamzdynų su plieniniais gaubtais projektavimas, įrengimas ir priežiūra (ISO/DIS 16440:2025)

ISO 16440:2016 specifies requirements, including corrosion protection, for the design, fabrication, installation and maintenance of steel-cased pipelines for pipeline transportation systems in the petroleum and natural gas industries in accordance with ISO 13623. NOTE 1 Steel casings can be used for mechanical protection of pipelines at crossings, such as at roads and railways and the installation of a casing at a highway, railway, or other crossing can be required by the permitting agency or pipeline operator. NOTE 2 This document does not imply that utilization of casings is mandatory or necessary. NOTE 3 This document does not imply that cased crossings, whether electrically isolated or electrically shorted, contribute to corrosion of a carrier pipe within a cased crossing. However, cased crossings can adversely affect the integrity of the carrier pipe by shielding cathodic protection (CP) current to the carrier pipe or reducing the CP effectiveness on the carrier pipe in the vicinity of the casing. Their use is not recommended unless required by load considerations, unstable soil conditions, or when their use is dictated by sound engineering practices.

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prEN 50463-3:2025 Archyvuotas

Komentavimo iki data 2026-01-02

Geležinkelio taikmenys. Energijos matavimas traukiniuose. 3 dalis. Duomenų apdorojimas

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).

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prEN ISO 11616 Viešoji apklausa

Komentavimo iki data 2026-01-15

Sveikatos informatika. Vaistų identifikavimas. Duomenų elementai ir struktūros, skirti unikaliam identifikavimui ir reglamentuotos informacijos apie farmacinius gaminius mainams (ISO 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.

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prEN 12896-6 Viešoji apklausa

Komentavimo iki data 2026-02-01

Viešasis transportas. Pamatinių duomenų modelis. 6 dalis. Informacija keleiviams

The document incorporates the following main data packages: - Trip Description; - Passenger Information Queries. It is composed of the following parts: - main document representing the data model for the concepts shared by the different fare domains covered by Transmodel (normative); - Annex A, containing the data dictionary and attribute tables, i.e. the list of all the concepts presented in the main document together with the definitions (normative); - Annex B presenting the model evolution (informative). - Annex C, providing details of the significant technical changes between this document and EN 12896 6:2019 (informative).

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ISO/IEC DIS 11770-4 Viešoji apklausa

Komentavimo iki data 2026-02-09

Informacijos saugumas. Raktų tvarkyba. 4 dalis. Mechanizmai, pagrįsti lengvai atskleidžiamais slaptažodžiais

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prEN 17151-2 Viešoji apklausa

Komentavimo iki data 2026-02-24

Plastikinių vamzdžių sistemos, skirtos paviršinio vandens beslėgiam požeminiam perdavimui ir laikymui. 2 dalis. Bandymo metodas talpyklų valkšnumo elgsenai nustatyti

This document specifies a test method for determining the compressive creep behaviour of boxes made of thermoplastic materials intended for use in a modular system for non-pressure underground conveyance and storage of surface water.

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prEN IEC 61439-6:2025 Archyvuotas

Komentavimo iki data 2025-12-31

Žemosios įtampos perjungimo ir valdymo įrenginių sąrankos. 6 dalis. Surenkamųjų šynų sistemos

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EN IEC 61591:2023/prA1:2025 Viešoji apklausa

Komentavimo iki data 2026-01-16

Siurbiamieji garų šalintuvai. Eksploatacinių charakteristikų matavimo metodai

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prEN ISO 9626 Viešoji apklausa

Komentavimo iki data 2026-01-29

Medicinos įtaisų gamybai naudojami nerūdijančiojo plieno adatų vamzdeliai. Reikalavimai ir bandymo metodai (ISO 9626:2025)

ISO 9626:2016 applies to rigid stainless steel needle tubing suitable for use in the manufacture of hypodermic needles and other medical devices primarily for human use. It provides requirements and test methods for the tubes manufactured for needles as component used in medical devices. Additional performance testing on the tube aspect may be required when the component is incorporated in the ready-to-use device. It specifies the dimensions and mechanical properties of steel tubing of designated metric sizes 3,4 mm (10 Gauge) to 0,18 mm (34 Gauge). It does not apply to flexible stainless steel tubing because the mechanical properties differ from those specified for rigid tubing in ISO 9626:2016. However, manufacturers and purchasers of flexible tubing are encouraged to adopt the dimensional specifications given in ISO 9626:2016.

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