Full Description 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[24], 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[25].
ISO/TR 24971:2020 Plus Redline history
2020ISO/TR 24971:2020 Medical devices -- Guidance on the application of ISO 14971
2013ISO/TR 24971:2013 Medical devices - Guidance on the application of ISO 14971