Overview
Whether you are an embedded software developer or an engineer 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, parts of the documentation required by IEC 62304 are automatically generated for regulatory compliance.
But how does Model-Based Design work in practice? And how do you get started? Join this webinar to learn the best practices for improving software quality while reducing development time and costs.
Highlights
- Requirements management and system architecture design
- Automated unit and system level testing with test report generation
- IEC 62304 supported workflow for FDA/MDR regulatory compliance
About the Presenter
Dr. Visa Suomi is the Medical Devices Industry Manager at MathWorks. He has over 10 years of international experience in the life sciences and healthcare sector, with an interdisciplinary background from the medical technology industry, academia, and clinical research. He holds a doctoral degree (DPhil in Healthcare Innovation) from the University of Oxford, UK, with the focus on translating academic and clinical research into commercial applications.
