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ISO/CD TS 23485

Medical devices — Quality management systems — Guideline for the application of ISO 13485:2016 ISO/CD TS 23485

General information

30.99   CD approved for registration as DIS   Jul 16, 2026

ISO

ISO/TC 210 Quality management and corresponding general aspects for medical devices

Technical Specification

Scope

This document provides guidance on the intent of the requirements in ISO 13485:2016, 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.

The document does not prescribe mandatory approaches to implementation or provide any preferred method of interpretation.

Life cycle

NOW

IN_DEVELOPMENT
ISO/CD TS 23485
30.99 CD approved for registration as DIS
Jul 16, 2026




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