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Average Medical Devices Expert Witnesses Court Fees
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Deposition Fee
Court Fee
This expert has over 15 years of experience in the medical device industry as a quality engineer, quality systems and complaint investigator with emphasis on cardiovascular devices. A Certified Quality Engineer and Biomedical Auditor, his expertise includes managing quality systems, design and development of new product lines, product risk management and complaint investigations. He currently serves as Principal quality management systems and business Consultant for an independent consulting firm in both medical device and other industries. His understanding of medical device firm operations and intimate familiarity with medical device requirements in both the US and other geographies make him an ideal expert to provide advice in determining both legal and regulatory requirements for medical device firms as well as users (clinicians).
President and Principal Consultant, An Independent Consultancy in MN
Master of Business Administration (MBA), Argosy University
Minnesota
This highler qualified expert has two decades of experience in basic and applied reserach in the thermal sciences. He has published well over 100 scientific papers dealing with biological heat transfer, burn injuries, and medical devices, among others. He has consulted for many companies in the medical device field and has presented well over 100 technical presentations at conferences and meetings. He is a Full Professor at a major Minnesota University.
Doctor of Philosophy (PhD)
Minnesota
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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.