MIDI specializes in developing intelligent, safe, and compliant SaMD and Medical Device solutions powered by AI and ML. Our team combines data scientists, engineers, clinicians, and regulatory specialists to advance patient care with streamlined workflows.
Every program begins in an AGILE-SCRUM sandbox, then advances beyond proof-of-concept into safe, reproducible, and regulatory-ready solutions. With built-in alignment to FDA, EU MDR/IVDR, ISO 13485, ISO 14971, and IEC 62304, our solutions are structured to scale with the needs of our clients
If you’re attending BECKERS HEALTHCARE conference and would like to discuss MIDI’s process for scaling innovation through Design, Engineering, Human Factors, Regulatory Strategy, and Commercialization, you can reach Chris directly; christopherm@midipd.com
Let’s explore how MIDI can help you shape your commercialization future.
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