About Me
- Appointed regulatory and clinical research subject matter expert with the International Organization for Standardization (ISO). Vice Convenor of ISO TC212/WG3 which authors international standards for in-vitro diagnostic products and liaison for ISO TC194/WG4 for medical devices.
- Progressive leadership roles at Fortune 200 medical device companies building high-performing clinical organizations and lean work processes that deliver business results
- 30+ years of proven experience in large multinational corporations and start-up firms that realized the commercial release of new medical technology
- Delivered 500+ medical device and IVD clinical trials for novel medical products that improved healthcare