Accelerate development throughout the product lifecycle.
Fast track development with an agile approach to managing highly regulated medical device documentation, risk, V&V, and development.
Unify your data, design, and teams
Bridge the gap between RA/QA and Developer teams with a software platform that gives visibility across projects, teams, and tasks in one place.
Quickly generate reusable and auto-updating documents like design control documentation, test reports, traceability matrices, ISO 14971 risk assessments and more.
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Streamline V&V and keep teams aligned across platforms by integrating IT tools with robust native integrations and access to our REST API for added support.
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Build a clear audit trail and demonstrate your risk-based approach to development in your next audit with end-to-end traceability across your design and development tools.
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Give RA/QA teams the information they need without adding to your workload in one centralized software SxMD platform and drive strong alignment.
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Develop faster and with confidence with IEC 62304 compliant workflows that alert you of missing or suspect items that need attention to ensure teams are working by the books.
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Quickly track and trace changes at any item level. Set up automatic alerts and workflows when there are changes that need to be reviewed and approved aligned with ISO 13485.
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Hear from our customers
“The integration between MatrixALM and GitLab makes it simpler for our developers to determine what each specification requires, and for designers to understand if and how a specification has been implemented – boosting the overall efficiency of our development process by 15%”
Nathalie Bosschaerts, Product Development Manager, Gabi SmartCare
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