Minnesota
Dr. Mark W. Kroll has 52 years of experience in Electrical and Biomedical Engineering. He earned his BS in Mathematics from the University of Minnesota, his MS and PhD in Electrical Engineering from the University of Minnesota - College of Science and Engineering, and his MBA from the University of St. Thomas. Formerly, this expert served as the Senior Vice President and Chief Technology Officer...
Minnesota
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...
Specialties:
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...
Specialties:
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A medical device expert witness provides specialized knowledge about the design, manufacturing, and usage of medical devices. They can testify on issues like product defects, patent infringement, or improper use.
Cases involving personal injury due to defective devices, malpractice claims related to incorrect device usage, patent disputes, and regulatory compliance issues often require a medical device expert witness.
They can provide insight into whether the device was designed or manufactured properly, if it met industry standards, and if instructions for use were clear and accurate.
Yes, experts may specialize in specific types of devices such as orthopedic implants, cardiovascular devices, diagnostic equipment, or prosthetics.
An expert familiar with FDA regulations can provide crucial testimony on whether a device met regulatory standards and if any violations could have contributed to harm.
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