Software Interface Design for Medical Devices: Enhancing Patient Outcomes and Minimizing Device Recalls

When it comes to medical devices, best practices for software interface design are not an option. They're an absolute necessity. This truth has been recognized by international standards organizations, successful medical device manufacturers, and key regulatory bodies, including the Food and Drug Administration. To shed light on effective medical device design, we'll explore:

• The role of poor design in medical errors
• Software design as a cause of device recalls
• Relevant international standards and FDA regulations
• The emergence of software as a medical device (SaMD)
• Best practices to follow when designing the interface for your next medical device