ISO/TR 80002-2:2017 Medical device software — Part 2: Validation of software for medical device quality systems

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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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Status: Active ChangeNumber: 1 InternationalClassificationCodeOfStandards: 11.040.01 TechnicalCommittee: ISO/TC 210 ActivatedDate: 13.06.2017 PagesCount: 84 Language: en

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