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).