Skip to main content
Back

ISO 10012:2026

Quality management — Requirements for measurement management systems

General information

Valid from 12.02.2026
Directives or regulations
None

Standard history

Status
Date
Type
Name
12.02.2026
Main
14.04.2003
Main
This document specifies the requirements for a measurement management system when an organization:

needs to demonstrate its ability to consistently ensure confidence in validity and reliability of measurement results and thereby to provide a consistent level of measurement quality for an organization’s products and services;
aims to rely on reliable and valid measurement results useful to enhance customer satisfaction and effectively apply its measurement management system processes;
implements processes for a measurement management system that enhance conformity with customer, statutory and regulatory requirements.

All the requirements of this document are generic. This document is applicable to any organization, regardless of its type or size, or the products and services it provides. This includes organizations manufacturing products and providing engineering services (except for calibration and test services included within the scope of ISO/IEC 17025).
This document is not intended to substitute requirements for, or to add requirements to, the general requirements for the competence of testing and calibration laboratories specified in ISO/IEC 17025.
NOTE For organizations that operate internal testing and calibration laboratories, the competence of those functions can be evaluated in accordance with ISO/IEC 17025.

Required fields are indicated with *

*
*
*
PDF
261.44 € incl tax
Paper
261.44 € incl tax
Standard monitoring

Customers who bought this item also bought

Main + amendment

EVS-EN ISO 15223-1:2021+A1:2025

Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021 + ISO 15223 1:2021/Amd 1:2025)
Newest version Valid from 01.12.2025
Main

EVS-EN ISO 10993-1:2026

Biological evaluation of medical devices - Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process (ISO 10993-1:2025)
Newest version Valid from 15.01.2026