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Matrix Requirements offers a pre-configured Tool Validation Project to its customers

01-Jul-2015 -

According to FDA regulations (Part 820.70) any software used in the production of medical devices must be validated. To simplify this task Matrix Requirements developed a specific project template. The white paper below summarizes the regulatory requirements and proposes a method to do this using MatrixALM.
Please contact us if you want to know more about this free offer.

Download White Paper


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