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

Office    651.430.7150
Mobile   651.393.6487

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).


Submissions made to FDA and other regulatory bodies


Miles hiked through the mountains in the U.S. and abroad


I have a decade’s worth of practical experience in a variety of areas. From assisting development teams, to supporting IDE studies, auditing advertising & promotional materials, and submitting adverse event reports, I help our clients get their products to the market, and keep them there.


Practice Areas:

  • Regulatory
  • Quality
  • Ad Promo Review