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sklademVydáno: 2020-07-22
PD CEN ISO/TR 24971:2020
Medical devices. Guidance on the application of ISO 14971
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| Označení normy: | PD CEN ISO/TR 24971:2020 |
| Počet stran: | 96 |
| Vydáno: | 2020-07-22 |
| ISBN: | 978 0 580 52399 1 |
| Status: | Corrigendum |
Popis
PD CEN ISO/TR 24971:2020
This standard PD CEN ISO/TR 24971:2020 Medical devices. Guidance on the application of ISO 14971 is classified in these ICS categories:
- 11.040.01 Medical equipment in general
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].