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ISO/TR 80002-2:2017

Medical device software -- Part 2: Validation of software for medical device quality systems

General information
Valid from 13.06.2017
Directives or regulations
None
Standard history
Status
Date
Type
Name
13.06.2017
Main
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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