ISO/TR 80002-2:2017
Current
The latest, up-to-date edition.
Medical device software — Part 2: Validation of software for medical device quality systems
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
English
06-13-2017
ISO/TR 80002-2:2017 applies to any software used in device design, testing, component acceptance, manufacturing, labelling, packaging, distribution and complaint handling or to automate any other aspect of a medical device quality system as described in ISO 13485.
ISO/TR 80002-2:2017 applies to
- software used in the quality management system,
- software used in production and service provision, and
- software used for the monitoring and measurement of requirements.
It does not apply to
- software used as a component, part or accessory of a medical device, or
- software that is itself a medical device.
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