IEC 81001-5-1:2021
2021-12
Abstract
This document defines the LIFE CYCLE requirements for development and maintenance of HEALTH SOFTWARE needed to support conformance to IEC 62443-4-1 – taking the specific needs for HEALTH SOFTWARE into account. The set of PROCESSES, ACTIVITIES, and TASKS described in this document establishes a common framework for secure HEALTH SOFTWARE LIFE CYCLE PROCESSES.
The purpose is to increase the CYBERSECURITY of HEALTH SOFTWARE by establishing certain ACTIVITIES and TASKS in the HEALTH SOFTWARE LIFE CYCLE PROCESSES and also by increasing the SECURITY of SOFTWARE LIFE CYCLE PROCESSES themselves.
It is important to maintain an appropriate balance of the key properties SAFETY, effectiveness and SECURITY as discussed in ISO 81001-1.
This document excludes specification of ACCOMPANYING DOCUMENTATION contents.
Buy together
Medical devices - the basics
This bundle combines essential ISO standards to provide a robust framework for quality management and risk management in the medical device industry.
- ISO 13485:2016
- ISO 13485:2016 A practical guide
- ISO 14971:2019
- ISO/TR 24971:2020
General information
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Status: PublishedPublication date: 2021-12Stage: International Standard published [60.60]
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Edition: 1
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Technical Committee :ISO/TC 215
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