Washington
Mr. Bradley W. Probst has 28 years of experience in the field of Biomedical Engineering. He earned his BS in Mechanical Engineering from the University of Louisiana at Lafayette and his MS in Biomedical Engineering from Tulane University. Formerly, this expert held roles as a Mechanical/Project Engineer at Wink Engineering, LLC, and as a Research Assistant at Tulane University. Currently, he...
Washington
This Washington-based expert has over 20 years of experience in chemistry and medical device research, specializing in polymer synthesis, polymer characterization, analytical chemistry, medical device design and intellectual property management. He received his BES in chemistry and photographic sciences from St. Cloud State University before earning his PhD in polymer chemistry from the...
Specialties:
Washington
Dr. Allan F. Tencer has 40 years of experience in Mechanical Engineering and Biomechanics. He earned his BEng, MEng, and Ph.D. in Mechanical Engineering from McGill University. Formerly, this expert served as the Director of the Biomechanics Laboratory at Harborview Medical Center. He also served as an Adjunct Professor of Mechanical Engineering and as a Professor of Orthopedic Surgery at the...
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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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