Medical Device Expert Witnesses in North Dakota

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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

South DakotaMinnesotaCustom source a Medical Device Expert

  • Medical Devices Expert Witness

    Review Fee $300/hr
    Deposition Fee $375/hr
    Court Fee $400/hr

    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

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  • Burn Injury & Medical Device Expert Witness

    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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Related Specialties

BiomedicalBiomedical Engineering

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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