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.

Trusted by 200+ SxMD & Medical Device Companies

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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Matrix ALM
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