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The downside of the FDA’s hands-off approach to regulating medical device software is that organizations have to constantly reinvent the wheel to define their own processes and static analysis rule selection criteria.

Other heavily-regulated embedded software industries, such as automotive, can lean on well-defined standards, such as MISRA, to ensure the security, safety, and reliability of their applications.

In this on-demand webinar, we'll explore how adopting MISRA software development standards can help you overcome the challenges associated with the FDA's "Least Burdensome" approach.

Session takeaways:

  • The costs associated with defining FDA-specific development process
  • Examples from MISRA and how they might apply to medical device software
  • How MISRA differs from other safety-critical standards, such as DO-178

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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.