My goal is to help companies create affordable healthcare solutions that improve patient outcomes or prevent disease. I am an experienced professional in the development and regulatory approval of medical devices through the entire product life-cycle.

I understand the regulatory requirements, and how to create compliant processes that add business value. I have experience in process improvement and training from R&D, business performance, and Quality perspectives.

My medical device experience includes external defibrillators and pacemakers, multi-parameter patient monitors, medical software, sterilizable accessories, ultrasound surgical devices, and electrical stimulation equipment.

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