Principal
CurrentMr. Terman concentrates his practice in medical device law, FDA regulatory issues, and litigation. While at Olsson Frank Weeda Terman Bode Matz PC, he has represented over 200 corporations, individuals and associations in civil, criminal and regulatory matters. Mr. Terman's expertise covers all areas of medical device law including the Quality System Regulation, Medical Device Reporting, IDE, 510(k) and PMA submissions. He has helped companies respond to FDA inspectional observations, Warning Letters and recalls, as well as civil penalty actions, injunctions, clinical disqualifications and criminal prosecutions.