Normas ISO
Filtrar:
ISO
ISO 22002-6:2025
En Vigor
2025-07-29
Prerequisite programmes on food safety — Part 6: Feed and animal food production
ISO
ISO 21001:2025
En Vigor
2025-07-07
Educational organizations — Management systems for educational
organizations — Requirements with guidance for use
ISO
ISO 2768-1:1989
En Vigor
1989-11-02
General tolerances — Part 1: Tolerances for linear and angular
dimensions without individual tolerance indications
ISO
ISO 22002-5:2025
En Vigor
2025-07-29
Prerequisite programmes on food safety — Part 5: Transport and storage
ISO
ISO/IEC 27002:2022
En Vigor
2022-02-15
Information security, cybersecurity and privacy protection — Information
security controls
ISO
ISO
ISO/IEC 29100:2024
En Vigor
2024-02-16
Information technology — Security techniques — Privacy framework
ISO
ISO 22000:2018/Amd 1:2024
En Vigor
2024-02-23
Food safety management systems — Requirements for any organization in
the food chain — Amendment 1: Climate action changes
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 14155:2026
En Vigor
2026-03-23
Clinical investigation of medical devices for human subjects — Good
clinical practice
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 29201:2012
En Vigor
2012-01-24
Water quality — The variability of test results and the uncertainty of
measurement of microbiological enumeration methods
ISO
ISO 10993-7:2026
En Vigor
2026-04-20
Biological evaluation of medical devices — Part 7: Ethylene oxide
sterilization residuals
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
