MatrixALM/QMS
Medical Devices documentation management
MatrixALM/QMS launched on January 30, 2020 with 2 votes. The site was still online in September 2026, 6 years on.
What it does
MatrixALM helps medical devices companies manage their technical documentation to ease generation of documents for CE marking or FDA 510(k). MatrixQMS helps managing the procedures and risks per ISO13485. Both products exclusively for medical devices!
Matrix One integrates requirements management, design control, eQMS, eIFU, cloud connectivity, and AI-powered compliance tools to help life science organizations build, launch, and support better and safer products
Matrix One brings together every element of regulated product development, from design control to post-market documentation, in one secure, cloud-based system. Whether you're managing requirements, quality events, eIFUs, or device connectivity, our AI-enabled solutions ecosystem keep your teams aligned and your compliance effortless. The best design control software for medical devices companies. The all-in-one cloud connectivity solution for medical device companies. Manage all the laboratory activities in one platform in a seamless and GxP compliant way. “With workflow automation we can import thousands of test cases from our third-party provider 95% faster than if we were performing the…from matrixone.health
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Matrix Requirements Medical2016 · matrixone.health · ▲5Keep your medical device documentation organized





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