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Average Medical Device Expert Witnesses Court Fees
$350/hr
Review Fee
$400/hr
Deposition Fee
$425/hr
Court Fee
This highly qualified engineer earned his BS and MS in mechanical engineering from California Polytechnic State University. He went on to earn his PhD in mechanical engineering from the University of California, Berkeley. He has over 10 years of experience conducting failure analysis for various products including biomedical devices. He formerly served as Principal Mechanical Engineer at COR Innovations, Inc., a biomedical device start-up. In this role, he was responsible for designing multiple functioning prototypes and designing and fabricating numerous electromechanical bench top apparatus' for materials testing and validation. He went on to serve as Senior Staff R&D Engineer at Abbott Vascular Structural Heart, where his primary role was serving as technical lead for improvements in their MitraClip device. He currently serves as Chief Technology Officer and co-founder of a medical device company that is focused on treating vaginal atrophy in breast cancer survivors and post-menopausal women through a novel and hormone-free, energy based therapy.
Co-Founder and Chief Technology Officer, A medical device company in OR
Doctor of Philosophy (PhD), University of California, Berkeley
Portland,
Oregon
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 University of Southern California. He is active in his field as a member of the American Chemical Society, is a highly-published author on the topics of polymer chemistry and medical devices, and holds 65 patents that have enhanced the field of polymer chemistry. Previously, he has served as a polymer chemist and then a senior polymer chemist at Medtronic, an adjunct professor of polymer chemistry at the University of St. Thomas, and a senior scientist at DexCom Inc. He also formerly served as an associate professor and then a professor of chemistry, as well the assistant dean of the college of science and technology and the interim assistant vice president and dean of graduate studies at Bloomsburg University. Currently, he serves as the vice president of intellectual property at a technology research lab in WA.
Founder and Chief Executive Officer, An analytical firm in VA
Doctor of Philosophy (PhD), University of Southern California
Front Royal,
Washington
This highly-qualified expert has extensive experience in automated external defibrillator (AED) program design and compliance. He earned his BS in public affairs from the University of Oregon and his JD from the Lewis & Clark Northwestern School of Law. He is a member of the Oregon State Bar and an advisory board member of the Sudden Cardiac Arrest Foundation and the National Center for Early Defibrillation. He has been the founder of several firms, including Lazar Jensen Geobel, Fios, Inc., and AED Risk Insights, Inc. Currently, this expert is the founder and president of an AED program compliance company that develops and publishes national AED program design guidelines that describe industry standards for AED programs and the AED Law Center.
Founder and President, An AED program compliance company
Juris Doctor (JD), Lewis & Clark Northwestern School of Law
Oregon
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What Can a Medical Device Expert Witness Opine On?
Device Design
Creating innovative medical device solutions.
Prototyping
Building initial models for testing.
Regulatory Submission
Preparing documents for regulatory approval.
Clinical Trials
Testing devices on human subjects.
Quality Assurance
Ensuring device compliance and safety.
Post-Market Surveillance
Monitoring device performance after launch.
FAQs for Medical Device Expert Witnesses
What is a medical device expert witness?
A medical device expert witness is a qualified specialist who explains device design, safety, and standards in legal cases. They assist by reviewing records, analyzing failures, writing reports, and testifying to clarify complex medical device issues.
What types of cases may benefit from the testimony of a medical device expert witness?
Medical device expert witnesses support product liability, design defect, manufacturing defect, failure-to-warn, malpractice, FDA compliance, and device-related injury and wrongful death cases.
How can a medical device expert witness evaluate alleged design defects?
A medical device expert witness evaluates alleged design defects by reviewing design records, testing data, standards compliance, clinical use, and alternative safer designs.
What qualifications should a medical device expert witness possess for complex litigation?
A medical device expert witness should have advanced clinical or engineering credentials, device-specific experience, regulatory knowledge, and proven testimony in complex litigation cases.
How does a medical device expert witness assess compliance with FDA regulatory standards?
A medical device expert witness assesses compliance with FDA regulatory standards by reviewing design, testing, labeling, quality systems, and documentation against applicable FDA regulations.
What is Expert Institute’s process for selecting medical device 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.