LDRA targets medical device design with IEC 62304 compliance

Tool suite now provides requirements traceability and compliance across complete software lifecycle with the integration of IEC 62304; the standard for software design of medical products, into its automated software verification, source code analysis and test tools. (11 hours ago)

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One Response to “LDRA targets medical device design with IEC 62304 compliance”

  1. Jane Bower says:

    This article talks about different software-based medical devices and the degree of patient risk if it fails to perform. The EC 62304 is a compliance program that assigns risk potentials to medical devices, A through C, and then classifies individual risk standards for each device depending on how dangerous it’s malfunction would be to the patient.