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ISO/IEC GUIDE 63:2019

ISO/IEC GUIDE 63:2019 Guide to the development and inclusion of aspects of safety in International Standards for medical devices

Summary

This document provides requirements and recommendations to writers of medical device standards on the inclusion of aspects related to safety in International Standards, based on well-established risk management concepts and methodology.

This document is applicable to any aspect related to the safety of people, property, the environment, or a combination of these.

In this document, the term "product" includes a medical device or a system consisting of one or more medical devices, possibly combined with non-medical devices.

Technical characteristics

Publisher International Organization for Standardization (ISO) / International Electrotechnical Commission (IEC)
Publication Date 08/12/2019
Edition 3.0
Page Count 26
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