Medical Devices Expert Witnesses in Vermont

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Medical Devices expert witnesses practice in a variety of fields, including product design, regulatory compliance, and clinical use. Some of the most common specialties include biomedical engineering, FDA regulatory affairs, human factors, and device failure analysis. They can opine on the effects of design defects, misuse, labeling errors, and adverse events on patient safety and outcomes.

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Average Medical Devices Expert Witnesses Court Fees

Review Fee

Deposition Fee

Court Fee

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  • Review Fee $150/hr
    Deposition Fee $375/hr
    Court Fee $500/hr

    This highly qualified expert has almost 30 years of experience as a perfusionist. He received a B.S. in Biology from Nazareth College of Rochester and a M.S. in Education from the State University of New York in Albany. He is board certified in Cardiovascular Perfusion and has been elected as a Fellow to the American Academy of Cardiovascular Perfusion where he previously served as President. He has published many articles on various perfusion methods and currently serves as Associate Professor and Clinical Coordinator in the Department of Cardiovascular Perfusion at a medical university in New York.

    Associate Professor, A Medical University in NY

    Master of Science (MS), State University of New York at Albany

    Baldwinsville,

    New York

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  • Review Fee $300/hr

    This highly qualified expert is the current director of the Office of Technology Transfer and Licensing at a major college in Massachusetts. He previously served as assistant director in the Office of Technology Transfer at Cold Spring Harbor Laboratory in New York and was an assistant professor in Virginia Commonwealth University. He has 10+ years of biomedical science research experience and a broad background combining experience in the life sciences, business, and patent law. He is a long time member of the Association of University Technology Managers and the Licensing Executives Society. He was among the first to earn a Certified Licensing Professional credential, and now serves as a current CLP Exam Development Committee member and AUTM International Professional Development Committee member. He is also a Registered Technology Transfer Professional. As a United States Patent and Trademark Office Registered Patent Agent, he has extensive experience in patent application and prosecution. He holds a PhD in molecular biology from Nankai University in China and an MBA from the University of Richmond. He is also the President and Board Chairman of the World Association of Chinese Technology Managers (WACTM).

    Director, Major College

    Master of Business Administration (MBA), University of Richmond

    Chestnut Hill,

    Massachusetts

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  • Review Fee $400/hr

    This expert received his undergraduate and doctoral degrees in Biomedical Engineering from Iowa State University. He has worked for and consulted with leading medical device, pharmaceutical & biotechnology companies ranging in size from start-ups to Fortune 100 companies. He also works on a regular basis for the FDA, Health Canada, the US & European Patent Offices, the Centers for Medicare and Medicaid Services, and other regulatory agencies around the world. As an internationally recognized expert, he presents frequently on cutting-edge medical technologies and conducts seminars for medical device, pharmaceutical and biotechnology companies.

    Adjunct Professor, A top university in DC and a medical school in PA

    Doctor of Philosophy (PhD), Iowa State University

    Carlsbad,

    Massachusetts

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  • Review Fee $350/hr
    Deposition Fee $500/hr

    This Boston based expert earned his Bachelor's of Science degree in electrical engineering from Tufts University. He began his career in medical device design at Siemens Medical Systems, thereafter serving as the Director of Engineering for Aspect Medical Systems, the developer of the world's first anesthesia monitor, which is now in 90% of operating rooms worldwide, and has served at least 200 million patients. He serves on the scientific advisory boards of several medical device firms including Safe-Op Surgical, a manufacturer of intraoperative nerve monitors.

    President, A technical consulting company to the medical device industry

    Bachelor of Science (BS), Tufts University

    Framingham,

    Massachusetts

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  • 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

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Related Specialties

What Can a Medical Devices Expert Witness Opine On?

Device Design

Creating functional medical device prototypes.

Regulatory Submission

Preparing documents for regulatory approval.

Quality Assurance Testing

Ensuring device safety and efficacy.

Clinical Evaluation

Assessing device performance in clinical settings.

User Training

Educating users on device operation.

Post-Market Surveillance

Monitoring device performance after launch.

FAQs for Medical Devices Expert Witnesses

What is the role of a medical devices expert witness?

A medical devices expert witness is a qualified specialist who explains device design, safety, and standards in legal cases. They assist by reviewing records, testing devices, writing reports, and testifying to clarify complex technical issues.

What types of cases can a medical device expert witness opine on?

A medical device expert witness opines on product defects, FDA compliance, labeling, adverse events, device failures, recalls, design, testing, manufacturing, and post‑market surveillance.

How can a medical devices expert witness strengthen product liability claims?

A medical devices expert witness strengthens product liability claims by explaining device design, testing, standards compliance, and causation in clear, evidence-based testimony.

What qualifications should attorneys prioritize in a medical devices expert witness?

Attorneys should prioritize a medical devices expert witness with advanced clinical or engineering credentials, device-specific experience, regulatory knowledge, and strong testifying history.

How does a medical devices expert witness evaluate device design compliance?

A medical devices expert witness evaluates device design compliance by reviewing design controls, risk management, testing data, regulatory standards, and documentation against FDA and ISO requirements.

What is Expert Institute’s process for selecting medical devices expert witnesses?

Expert Institute delivers a tailored approach to connect you with top-tier experts. We identify actively practicing professionals who meet your exact criteria for specialty, experience, litigation background, fee structure, credentials, location, and more.

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