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.
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We do not use cookies to:
try to identify you as a person
send you spam
do any kind of marketing activities
The cookies are set and evaluated by these third-party tools:
Google Analytics (to create anonymous usage statistics of our website)
Google reCAPTCHA (to avoid that you need to fill out captchas when submitting forms)
Slaask (to add the possibility for you to chat with us using slack)
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