Medical Device Expert Witnesses in Idaho

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Medical Device expert witnesses practice in a variety of fields, including biomedical engineering, regulatory compliance, and clinical practice. Some of the most common specialties include product design, FDA approval, quality control, human factors, and post-market surveillance. They can opine on the effects of device defects, labeling, testing, adverse events, and standard of care in litigation.

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Average Medical Device Expert Witnesses Court Fees

$350/hr

Review Fee

$400/hr

Deposition Fee

$425/hr

Court Fee

Find Medical Device Expert Witnesses in nearby states

  • Review Fee $200/hr
    Deposition Fee $300/hr
    Court Fee $300/hr

    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

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  • Review Fee $400/hr
    Deposition Fee $450/hr
    Court Fee $500/hr

    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

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  • Review Fee $300/hr
    Deposition Fee $500/hr

    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.

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