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ISO 15195:2018/DAmd 1 Public enquiry
Comment end date 2026-09-24
Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement procedures — Amendment 1
ISO/DIS 6575 Public enquiry
Comment end date 2026-09-19
Fenugreek, whole or ground (powdered) — Specification
ISO 20109:2025/DAmd 1 Public enquiry
Comment end date 2026-09-12
Simultaneous interpreting — Equipment — Requirements — Amendment 1
ISO/IEC DIS 27007 Public enquiry
Comment end date 2026-09-01
Information security, cybersecurity and privacy protection — Guidelines for information security management systems auditing
ISO/IEC DIS 27004 Public enquiry
Comment end date 2026-09-01
Information technology — Security techniques — Information security management — Monitoring, measurement, analysis and evaluation
ISO/DIS 9002 Public enquiry
Comment end date 2026-08-24
Quality management systems — Guidelines for the application of ISO 9001

This document provides guidance on the intent of the requirements in ISO/DIS 9001 ISO 9001:2026, with examples of possible steps an organization can take to meet the requirements. It does not add to, subtract from, or in any way modify those requirements. This document does not prescribe mandatory approaches to implementation or provide any preferred method of interpretation.

ISO/DIS 5565-1.2 Public enquiry
Comment end date 2026-08-04
Vanilla (Vanilla planifolia Andrews, syn. Vanilla fragrans Ames, and Vanilla x tahitensis JW Moore) — Part 1: Specification
ISO/IEC DIS 25093-1 Public enquiry
Comment end date 2026-08-17
Cybersecurity — Confidential computing — Part 1: Overview and concepts
ISO/IEC DIS 10267 Public enquiry
Comment end date 2026-08-16
Information technology — Data usage — Methods to quantify the amount of personal information in a dataset
ISO/DIS 20228 Public enquiry
Comment end date 2026-08-13
Interpreting services — Legal interpreting — Requirements
ISO/DIS 13682-1 Public enquiry
Comment end date 2026-08-15
Laser and laser related equipment — Determination of the properties of ultrashort laser pulses — Part 1: Vocabulary and symbols
ISO/DIS 13682-2 Public enquiry
Comment end date 2026-08-15
Laser and laser related equipment — Determination of the properties of ultrashort laser pulses — Part 2: Autocorrelation measurement method
ISO/IEC DIS 25330-1 Public enquiry
Comment end date 2026-08-07
Information security — Oblivious transfer — Part 1: General
ISO/DIS 25459 Public enquiry
Comment end date 2026-08-09
In vitro diagnostic medical devices — Requirements for determining commutability of certified reference materials used as secondary calibrators or trueness controls
ISO/IEC DIS 27555 Public enquiry
Comment end date 2026-08-05
Information security, cybersecurity and privacy protection — Guidelines on personally identifiable information deletion
ISO/DIS 23565 Archived
Comment end date 2026-07-31
Biotechnology — Bioprocessing — General requirements and considerations for equipment systems used in the manufacturing of cellular therapeutic products

This document specifies minimum requirements and general considerations for equipment, consisting of hardware, software and consumables, used in the manufacturing of cellular therapeutic products. This includes equipment for processing cellular therapeutic products starting from cell isolation/selection, expansion, washing, volume reduction, final formulation and preparation prior to cryopreservation for storage of cellular therapeutic products. This document provides guidance on the design, use and maintenance of equipment and equipment systems to both equipment suppliers and equipment users including aspects such as the target parties, i.e. equipment supplier or equipment user, and the phase of the involved task, i.e. design, use, or maintenance. This document is applicable to any unit operation system, that is intended to be used, either alone or in combination, for the manufacture of cellular therapeutic products by meeting equipment user requirements. It is applicable to equipment used for the purpose of monitoring the equipment status. This document does not apply to: — processing equipment for cellular therapeutic products used at the point of care; — equipment used for analytical purposes; — biosafety cabinets, general cell culture equipment (such as CO2 incubators, etc.); — software to control multiple equipment systems or multiple unit operations.

ISO/DIS 25608 Archived
Comment end date 2026-07-25
Healthcare organization management — Smart hospitals — RTLS for portable devices

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