This testifying expert witness has over 15 years of experience designing embedded hardware and firmware for medical instruments.  He is an expert in FDA QSR, ISO 13485, and the IEC 60601 regulatory process.  This expert is a published author and has testified in many U.S. District Courts and the U.S. International Trade Commission.

Areas of Expertise

  • Embedded system design for safety-critical systems
  • System architecture of electronic subsystems for medical products
  • Regulatory processes for medical device design

Education

B.S. in Computer Engineering