When you work with me, you work directly with me from the initial kickoff through project closeout. We discuss the project together, define the scope, and all communication and updates come straight from me. You'll get my years of medical device design and human factors experience throughout the entire engagement — not just at the proposal stage.

I stay personally involved and accountable for every project. I keep my practice intentionally lean, which means less overhead, fewer layers between decisions and action, and no pressure to fit a project into the capabilities of a large internal team. The work is driven by what your project needs, not by who happens to be on payroll.

When additional expertise or capacity is needed, I bring in experienced specialists with full transparency, ensuring you always know who is contributing and why. The result is a flexible team tailored to the project, with a single point of contact and accountability throughout.

Over the past twenty plus years, I've helped develop medical devices through every stage of development — from early user research and clinical observation through concept development, CAD, usability testing, and design for manufacturing. I've spent time in operating rooms, clinics, and patient care environments learning firsthand how devices are actually used, then translating those insights into products that are safer, easier to use, and better aligned with clinical workflows.

My experience includes cardiology, patient monitoring, drug delivery, surgical devices, and home healthcare products, along with work in human factors and FDA-focused usability engineering. Over time, that experience has given me a practical understanding of how devices fit into clinical workflows, what matters most to healthcare providers and patients, and where design decisions can have the greatest impact.