My Story

I am a human factors expert with nearly a decade of experience in medical device development. During that time I have built human factors procedures from scratch, created project documentation for several successful regulatory submissions (e.g., 510k, IDE, etc.), and helped steer project teams to make safer, more usable products. 

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With my PhD in human factors and cognitive science, I've leveraged my education to help teams design products in view of the expectations and limitations of the user. 

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I've served on committees to review and update guidance documents (e.g. HE75) and enjoy staying on the cutting edge of the human factors research to not only see what is current best practice but anticipate future trends in design and regulation.

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