Theodore Thompson J.D., R.A.C., Associate Attorney

Theo specializes in quality and regulatory affairs. He has experience in regulatory submissions to FDA, EU Notified Bodies and Health Canada. Before joining Gardner Law, Theo worked at Medtronic as a Senior Regulatory Affairs Specialist where he worked on submissions, including cybersecurity-specific submissions to FDA, license renewals, and annual registrations. He also worked as an FDA and EU Medical Device Reporting Specialist. Prior to Medtronic Theo worked as a project attorney for Robins, Kaplan, Miller, & Ciresi, LLP and Nichols Kastor, PLLP. Theo has also received the Regulatory Affairs Certification (RAC), the HealthCare Information Security and Privacy Practitioner (HCISPP) certification, and is a Certified Medical Device Auditor (CMDA).