Bring safe products to market faster.
Support rapid SxMD growth with a certified software platform for ISO 13485 and ISO 27001 that empowers design and quality teams.
Supercharge intelligent collaboration
Enable seamless alignment between teams and navigate the regulatory landscape with confidence.
Accelerate medical device regulatory approval
Connect your design control and quality management in a central location for complete traceability to make it easy to perform gap & risk analysis and generate compliant documentation.
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Drive commercialization success
Meet FDA and MDR regulatory standards with an easy-to-use, flexible software platform that supports the full product lifecycle from ideation to market launch.
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Bridge the gap between teams and workflows
Break down data barriers by integrating your team's tools to help you fast track compliant, quality development without compromising agile workflows.
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Mitigate and reduce risk across the product lifecycle
Proactively manage risk throughout the entire lifecycle by linking design controls and quality management to easily prove risk control during audits.
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Hear from our customers
“Our demo accounts from Matrix Requirements grew into fully fledged production deployments of MatrixALM and MatrixQMS almost immediately.”
Rutger Flink, CEO and Founder, PulmoTech
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