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prEN ISO 14627 Viešoji apklausa

Komentavimo iki data 2025-10-07

Techninė keramika (modernioji keramika, modernioji techninė keramika). Silicio nitrido medžiagų, iš kurių gaminami riedėjimo guolių rutuliukai, atsparumo įtrūkiams bandymo įspaudžiant kambario temperatūroje metodas (ISO 14627:2012)

This International Standard describes a test method that covers the determination of fracture resistance of silicon nitride bearing balls at room temperature by the indentation fracture (IF) method, as specified in ISO 26602. This International Standard is intended for use with monolithic silicon nitride ceramics for bearing balls. It does not include other ceramic materials. This International Standard is for material comparison and quality assurance. Indentation fracture resistance, KI, IFR as defined in this International Standard is not to be equated to fracture toughness determined using other test methods such as KIsc and KIpb.

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prEN ISO/IEC 27019 Viešoji apklausa

Komentavimo iki data 2025-10-19

Informacijos saugumas, kibernetinis saugumas ir privatumo apsauga. Informacijos saugumo kontrolės priemonės, skirtos energetikos sektoriui (ISO/IEC 27019:2024)

This document provides information security controls for the energy utility industry, based on ISO/IEC 27002:2022, for controlling and monitoring the production or generation, transmission, storage and distribution of electric power, gas, oil and heat, and for the control of associated supporting processes.

Skaityti, komentuoti projektą Peržiūrėti metaduomenis

ISO/DIS 24952 Viešoji apklausa

Komentavimo iki data 2025-11-16

Biotechnologija. Biobankai. Bendrieji reikalavimai (pusiau) automatizuotai laikymo ir paėmimo įrangai

This document specifies general requirements for (semi-)automated storage and retrieval equipment for biobanking, including their design, customization and installation, (semi-)automated storage and retrieval functions, performance, personnel, facility environment, operation and maintenance. This document specifies consumable and software systems for (semi-)automated storage and retrieval equipment for biobanking. This document is applicable to manufacturers of (semi-)automated storage and retrieval equipment, as well as to biobanks that use or operate such equipment. This document is applicable to manufactures of consumables of (semi-)automated storage and retrieval equipment.

Skaityti, komentuoti projektą Peržiūrėti metaduomenis

prEN 18223 Archyvuotas

Komentavimo iki data 2025-09-02

Skaitmeninis gaminio pasas. Sistemų sąveikumas

The scope of this document includes: — the semantic description of a product, including its properties where relevant and the semantic aspects to represent the product lifecycle; — a common information model allowing for the implementation of data dictionary systems; — metadata models and formats to be used in exchange and representation, allowing for the integration of dictionaries; — rules on how to systematically use such metadata models when developing product group specific data models and dictionaries; — technical and organizational interoperability. This document follows the approach of standard interoperability layers and proposes the following aspects in this regard.

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prEN ISO 19157-3 Archyvuotas

Komentavimo iki data 2025-09-16

Geografinė informacija. Duomenų kokybė. 3 dalis. Duomenų kokybės matų registras (ISO/DIS 19157-3:2025)

This International Standard specifies the process of establishing, maintaining and publishing a register of data quality measures in compliance with ISO 19135-1:2015. It identifies and describes the components and content structure of a register for data quality measures, and the registration and maintenance procedure. This International Standard also specifies the required machine-readable (XML, Geospatial-API) implementation of the register and the procedure of accessing and use of the register.

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prEN ISO 10325 Viešoji apklausa

Komentavimo iki data 2025-10-12

Pluoštiniai lynai. Didžiamodulis polietilenas. 8 vijų pintiniai lynai, 12 vijų pintiniai lynai ir dengtieji lynai (ISO/DIS 10325:2025)

This document specifies requirements for 8-strand braided ropes, for 12-strand braided ropes, and for covered rope constructions for general purpose made of high modulus polyethylene (HMPE), and gives rules for their designation. Many different types and grades of HMPE fibre exist which are commonly used to produce rope products. This document does not cover all variations in strength or product performance. The rope manufacturer is consulted to ensure the intended design meets the requirements of the application.

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prEN 2243-7 Viešoji apklausa

Komentavimo iki data 2025-10-21

Aerospace series - Structural adhesives - Test methods - Part 7: Determination of the flow of adhesive film

Skaityti, komentuoti projektą Peržiūrėti metaduomenis

prEN ISO/ASTM 52922 Naujas

Komentavimo iki data 2025-11-18

Adityvioji gamyba. Projektavimas. Metalų prilydymas naudojant kryptinį energijos šaltinį (ISO/ASTM DIS 52922:2025)

This document specifies the features of Directed Energy Deposition (DED) and provides detailed design recommendations. This document also provides a state-of-the-art review of design guidelines associated with the use of DED by bringing together relevant knowledge about this process and by extending the scope of ISO/ASTM 52910.

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prEN 18219 Archyvuotas

Komentavimo iki data 2025-09-02

Skaitmeninis gaminio pasas. Unikalieji identifikatoriai

This document defines the principles and specifies the requirements and guidelines for unique product identifiers, unique economic operator identifiers, and unique facility identifiers used in digital product passports. It covers the following areas: a) global uniqueness; b) persistence; c) syntax; d) semantics; e) interoperability; f) openness. This document accommodates unique product identifiers at three granularity levels of specificity: model, batch, or individual item, to support various operational needs. This document describes identification (ID) schemes that use issuing agencies, self-issuing systems, or a combination of both.

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ISO/DIS 23494-2 Archyvuotas

Komentavimo iki data 2025-09-15

Biotechnologija. Kilmės informacijos modelis, taikomas biologinei medžiagai ir duomenims. 2 dalis. Bendrasis kilmės informacijos modelis

This document specifies a common model for generating, maintaining, and provisioning provenance information on objects, such as biological material and data. This document also specifies requirements for provenance information serialization to achieve its interoperability. The provenance information covers any information relevant to the traceability, quality and fitness for purpose of the biological material and data generated throughout the life cycle of the biological material from collection to analysis, including data originating from analytical procedures applied to the biological material and further processing of the data. This document is applicable to organizations, authorities and industries that are: a) acquiring, collecting, processing, testing, analyzing, storing, or distributing biological material in biotechnology and biomedicine (e.g., biobanks, laboratories, biomedical research as well as biotechnological development or production); b) generating, collecting, analyzing, processing, or storing data on and related to biological material (e.g., biobanks, laboratories, developers, manufacturers, or other institutions and commercial organizations in biotechnology or biomedicine); c) generating, collecting, analyzing, processing, or storing data or digital objects in biotechnology and biomedicine (e.g., in vitro/in vivo/in silico diagnostics developers and manufacturers, or other institutions and commercial organizations in the domain). d) Manufacturing devices or software for the afore mentioned tasks or providing facilities for these tasks. This document is also applicable to providers of services related to provenance information management (e.g., provenance information generation, storage, provision, or validation). Customers, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies, and others can use this document in confirming or recognizing the competence of the aforementioned parties. This document does not apply to biological material and data used for medical diagnosis and therapy. NOTE 1 This document can be applied by organizations performing laboratory or research activities as well as other activities in biotechnology and biomedicine. NOTE 2 International, national, or regional regulations or requirements can also apply to specific topics covered in this document.

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