MEET THE TEAM
Thomas Lawson, PhD,
Regulatory Affairs and Quality Assurance Consultant
Over 30 years of experience in regulatory affairs and quality assurance, in both start-up and Fortune 500 companies, involving writing over 50 regulatory filings for commercialization of medical devices in 15 countries, authoring over thirty-five 510(k) submissions, establishing quality systems in 7 start-ups, and gaining CE marking for 12 devices. PhD in pathology from the University of California, Berkeley.