This document provides guidance on the development, implementation and maintenance of a risk management system for medical devices according to ISO 14971:2019.
The risk management process can be part of a quality management system, for example one that is based on ISO 13485:2016, but this is not required by ISO 14971:2019. Some requirements in ISO 13485:2016 (Clause 7 on product realization and 8.2.1 on feedback during monitoring and measurement) are related to risk management and can be fulfilled by applying ISO 14971:2019. See also the ISO Handbook: ISO 13485:2016 — Medical devices — A practical guide.
Status: PublishedPublication date: 2020-06
Edition: 2Number of pages: 87
Technical Committee: ISO/TC 210 Quality management and corresponding general aspects for medical devices
Buy this standard
|std 1 208||PDF + ePub|
|std 2 250||PDF + ePub + Redline|
|std 3 208||Paper|