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Coverity White Paper

Test Your Software Code, Manage Safety Risks, Control Compliance

As devices and software are becoming more complex, are you prepared for this ever-changing landscape of software compliance standards?  Learn now how Coverity can help you to control the quality of your code and manage the potential safety risks associated with product failure. 

Three Steps to Improving your Software Quality: Define, Test and Control

Our latest whitepaper entitled, “Governance, Risk, and Compliance: Medical Device Software Validation,” provides an understanding on how to establish a three-step solution that will assist you in the regulatory process while building long-term best practices into your software development cycle. 

This whitepaper is a must-read for anyone developing medical devices based on complex software code.


Did you happen to see last week’s New York Times front page headline, “Study of Medical Device Rules is Attacked, Unseen?” The article was one of many that highlighted the latest study from the Institute of Medicine calling for a tougher FDA approval process on a wide variety of software-driven medical devices. 

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