Committee Draft
ISO/CD TS 23485
Medical devices — Quality management systems — Guideline for the application of ISO 13485:2016
Reference number
ISO/CD TS 23485
Edition 1
Committee Draft
ISO/CD TS 23485
90565
A draft is being reviewed by the committee.

Abstract

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.

General information

  •  : Under development
    : CD approved for registration as DIS [30.99]
  •  : 1
  • ISO/TC 210
  • RSS updates

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