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ISO

ISO 8573-1:2010

En Vigor
2010-04-06
Compressed air — Part 1: Contaminants and purity classes
ISO

ISO/IEC 29100:2024

En Vigor
2024-02-16
Information technology — Security techniques — Privacy framework
ISO

ISO 15223-1:2021/Amd 1:2025

En Vigor
2025-03-03
Medical devices — Symbols to be used with information to be supplied by the manufacturer — Part 1: General requirements — Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specific
ISO

ISO 14155:2026

En Vigor
2026-03-23
Clinical investigation of medical devices for human subjects — Good clinical practice
ISO

ISO 11352:2025

En Vigor
2025-09-01
Water quality — Estimation of measurement uncertainty based on validation and quality control data
ISO

ISO/IEC 19790:2025

En Vigor
2025-02-26
Information security, cybersecurity and privacy protection — Security requirements for cryptographic modules
ISO

ISO 10993-17:2023/Amd 1:2025

En Vigor
2025-11-18
Biological evaluation of medical devices — Part 17: Toxicological risk assessment of medical device constituents — Amendment 1
ISO

ISO 50001:2018

En Vigor
2018-08-20
Energy management systems — Requirements with guidance for use
ISO

ISO 10993-7:2026

En Vigor
2026-04-20
Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals
ISO

ISO 13485:2016

En Vigor
2016-02-25
Medical devices — Quality management systems — Requirements for regulatory purposes
ISO

ISO/IEC 5055:2021

En Vigor
2021-03-30
Information technology — Software measurement — Software quality measurement — Automated source code quality measures
ISO

ISO/IEC 7810:2019

En Vigor
2019-12-18
Identification cards — Physical characteristics
ISO

ISO 59010:2024

En Vigor
2024-05-22
Circular economy — Guidance on the transition of business models and value networks
ISO

ISO 11137-1:2025

En Vigor
2025-04-02
Sterilization of health care products — Radiation — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
ISO

ISO 16140-3:2021/Amd 1:2025

En Vigor
2025-08-15
Microbiology of the food chain — Method validation — Part 3: Protocol for the verification of reference methods and validated alternative methods in a single laboratory — Amendment 1: Protocol for verification of validated identification methods of microorganisms
ISO

ISO/IEC 30141:2024

En Vigor
2024-08-27
Internet of Things (IoT) — Reference architecture
ISO

ISO/IEC 33001:2015

En Vigor
2015-02-27
Information technology — Process assessment — Concepts and terminology
ISO

ISO/TS 37008:2023

En Vigor
2023-07-28
Internal investigations of organizations — Guidance
ISO

IWA 48:2024

En Vigor
2024-11-14
Framework for implementing environmental, social and governance (ESG) principles
ISO

ISO 10012:2026

En Vigor
2026-02-12
Quality management — Requirements for measurement management systems