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Matrix Requirements offers ALM and QMS software for medical device firms, ensuring compliance with ISO 13485 and ISO 27001. It enables traceability of requirements, tests, and risks, while integrating with tools like Jira and GitHub—helping teams develop safe products faster and meet global regulations.
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Comprehensive Compliance Support:
Matrix Requirements offers robust support for regulatory standards like ISO 13485 and FDA 21 CFR Part 820, providing built-in risk and CAPA modules that require minimal adjustment to suit business needs.
Seamless Integration with Development Tools:
The platform integrates effectively with tools such as Jira, facilitating agile workflows and enhancing collaboration between engineering and quality teams.
User-Friendly Interface:
Users find the software easy to navigate, with intuitive features that streamline documentation, requirements management, and planning within the ALM module.
Limited Reporting Capabilities:
Some users have noted that the reporting package for data analysis could be improved to allow for better analysis within Matrix.
Basic Table Functions:
Internal table functions could be enhanced to allow for features like autofill and freezing of column and row headers, which are currently lacking.
Complex Setup Process:
A few users have mentioned that the initial setup and configuration can be complex, requiring a steep learning curve to fully utilize all features.
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