In Software as a Medical Device (SaMD) and Software in a Medical Device (SiMD), the practice of managing requirements is crucial.
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As technology continues to integrate deeper into the healthcare landscape, the complexity and regulatory scrutiny of medical software also increase.
Requirements Management ensures that these technologies not only meet specific clinical needs but also comply with stringent regulatory standards that govern their safety, reliability, and effectiveness.
Learn more about Requirements Management in Medical Devices here:
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