Whether you are a software developer, an engineer, or a R&D manager designing a medical device, software quality is critical for patient safety.
Model-Based Design incorporates verification and validation into the software development workflow. As a result, the software is comprehensively tested and verified before you integrate it into a medical device. In addition, most of the documentation required by the IEC 62304 standard are automatically generated for regulatory compliance.
But how does Model-Based Design work in practice? And how do you get started?
Read this white paper to learn:
- The basics of Model-Based Design for medical devices
- Case studies from the leading medical device companies
- Tips and best practices for getting started