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The FDA recommends implementing a coding standard during medical device software development. In practice, this means running a static analysis tool to detect any problematic constructs that could lead to problems down the road. 

But if you think you can simply download an analyzer and go, you might consider that the FDA requires documented details associated with code quality activities.

What standard are you going to check against? What rules in the analyzer cover the standard? Which rules are you suppressing? The implementation of static analysis is enough to cause headaches, gastrointestinal discomfort, and other side-effects.

This webinar prescribes some static analysis implementation best practices to relieve your FDA compliance symptoms, including:

  • The benefits of static analysis and what to look for in an analyzer
  • How to automate static analysis execution
  • How to integrate static analysis within your software development processes.
  • How to reduce noise and stop wasting time manually triaging results

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ABOUT PARASOFT

Parasoft provides innovative tools that automate time-consuming testing tasks and provide management with intelligent analytics necessary to focus on what matters. Parasoft’s technologies reduce the time, effort, and cost of delivering secure, reliable, and compliant software, by integrating static and runtime analysis; unit, functional, and API testing; and service virtualization. Parasoft supports software organizations as they develop and deploy applications in the embedded, enterprise, and IoT markets. With developer testing tools, manager reporting/analytics, and executive dashboarding, Parasoft enables organizations to succeed in today’s most strategic development initiatives — agile, continuous testing, DevOps, and security.