Compudu

Bridging AI Prototypes to Production-Ready Medical Devices

AI Productionization

Transform prototype algorithms into robust, scalable systems with clean code, automated testing, and maintainable architecture.

Navigate FDA, CE Marking, and ISO 13485 compliance with structured development processes and documentation support.

Design workflows to bridge gaps between data scientists, engineers, and regulatory teams.

Expertise, Network and Proven Track Record

7+ years implementing AI in regulated environments (Philips, Biogen, MoCA Cognition).

Partner with a network of regulatory experts and clinical advisors to fill knowledge gaps.

Successfully shipped medical devices and AI tools from prototype to production.

This is how it works

Align on your goals and regulatory requirements.

Review prototypes, codebase, and documentation.

Build a phased plan for production and compliance.

Hands-on coding, process design, or team training.

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