Defective medical device expert witnesses analyze product design, manufacturing, labeling, and post-market performance to assess whether devices met safety and quality standards. They are often biomedical engineers, regulatory specialists, or clinicians who evaluate device failures, risk management, human factors, and compliance with FDA and industry requirements.
Medical Device Product Development Expert Witness
Medical Device Product Development Expert Witness
- Review Fee
- $600/hr
- Deposition Fee
- $600/hr
- Court Fee
- $600/hr
This expert has experience in Medical devices since 1992. Design experience since 1986. Areas of expertise include full life cycle product development of medical devices from conception through development including manufacturing, bench testing, verification, validation, packaging, labeling, clinical trials, regulatory approval, marketing, and sales training. Granted 28 patents (others pending), 7 awards, designs published by Life Magazine, was recognized as one of 100 notable people in the medical device industry by the Medical Device & Diagnostic Industry (MD&DI) publication in June 2008. This expert recently served as chairman of the Medical Device & Manufacturing Conference in 2014.
President, A medical device development consultancy in NH
Master of Science (MS), North Carolina A&T State University
Dover,
New Hampshire