Medical Devices Expert Witnesses in Rhode Island

We’ll help you retain an industry-leading Medical Devices expert

Medical Devices expert witnesses practice in a variety of fields, including product design, regulatory compliance, and clinical use. Some of the most common specialties include biomedical engineering, FDA regulatory affairs, human factors, and device failure analysis. They can opine on the effects of design defects, misuse, labeling errors, and adverse events on patient safety and outcomes.

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Average Medical Devices Expert Witnesses Court Fees

Review Fee

Deposition Fee

Court Fee

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  • Review Fee $300/hr

    This highly qualified expert is the current director of the Office of Technology Transfer and Licensing at a major college in Massachusetts. He previously served as assistant director in the Office of Technology Transfer at Cold Spring Harbor Laboratory in New York and was an assistant professor in Virginia Commonwealth University. He has 10+ years of biomedical science research experience and a broad background combining experience in the life sciences, business, and patent law. He is a long time member of the Association of University Technology Managers and the Licensing Executives Society. He was among the first to earn a Certified Licensing Professional credential, and now serves as a current CLP Exam Development Committee member and AUTM International Professional Development Committee member. He is also a Registered Technology Transfer Professional. As a United States Patent and Trademark Office Registered Patent Agent, he has extensive experience in patent application and prosecution. He holds a PhD in molecular biology from Nankai University in China and an MBA from the University of Richmond. He is also the President and Board Chairman of the World Association of Chinese Technology Managers (WACTM).

    Director, Major College

    Master of Business Administration (MBA), University of Richmond

    Chestnut Hill,

    Massachusetts

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  • Review Fee $400/hr

    This expert received his undergraduate and doctoral degrees in Biomedical Engineering from Iowa State University. He has worked for and consulted with leading medical device, pharmaceutical & biotechnology companies ranging in size from start-ups to Fortune 100 companies. He also works on a regular basis for the FDA, Health Canada, the US & European Patent Offices, the Centers for Medicare and Medicaid Services, and other regulatory agencies around the world. As an internationally recognized expert, he presents frequently on cutting-edge medical technologies and conducts seminars for medical device, pharmaceutical and biotechnology companies.

    Adjunct Professor, A top university in DC and a medical school in PA

    Doctor of Philosophy (PhD), Iowa State University

    Carlsbad,

    Massachusetts

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  • Review Fee $350/hr
    Deposition Fee $500/hr

    This Boston based expert earned his Bachelor's of Science degree in electrical engineering from Tufts University. He began his career in medical device design at Siemens Medical Systems, thereafter serving as the Director of Engineering for Aspect Medical Systems, the developer of the world's first anesthesia monitor, which is now in 90% of operating rooms worldwide, and has served at least 200 million patients. He serves on the scientific advisory boards of several medical device firms including Safe-Op Surgical, a manufacturer of intraoperative nerve monitors.

    President, A technical consulting company to the medical device industry

    Bachelor of Science (BS), Tufts University

    Framingham,

    Massachusetts

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  • Review Fee $480/hr
    Deposition Fee $480/hr
    Court Fee $480/hr

    This certified Regulatory Affairs Professional has more than 20 years of experience ensuring compliance with the FDA. Throughout his career, he has managed 510(k) submissions, reviews, appeals, and clinical trials for a multitude of devices with applications ranging from dentistry to cardiology and neurology. Prior to launching his current consultancy, he served as a Director of Regulatory Affairs at medical device firms that manufacture class II and class III products. Have experience with: Catheters/Stents: IV administration sets, peripheral perfusion/infusion catheters, coronary perfusion/infusion catheters, thoracic catheters, chest drains and blood bags, embolectomy catheters, thrombus aspiration catheters, PTA, PTCA, CVC, ECMO, retrograde and antegrade hemodialysis catheters, urethral and ureteral catheters/stents, insulin administration, Closed System drug Transfer Devices (CSTD), non-roller cardiopulmonary bypass pumps and catheters, coronary and peripheral BMS, peripheral covered stents, aortic covered stents, DES, ureteral stents, urological stents, esophageal stents, intracranial aneurysm stents, pericardium covered stents, vascular grafts and vascular grafts with helix or nitinol reinforcement, and vascular patches. Biomaterials: bone void fillers, resorbable implants, hydroxyl appetite, hyaluronic acid, dental impression materials, PEEK, calcium carbonate, Beta TCP, imaging contrast agents, hydrogel dressings, lubricious coatings, artificial saliva, contact lenses and contact lens solutions, antimicrobial coatings, antithrombotic coatings, IIb/IIIa inhibitors, mTOR inhibitors, and omega3 coatings, injectors and pens, antimicrobial wound cleanser and bandages. Orthopedic/Dental: ACL/PCL screws, suture anchors, tacks, staples, spinal cages, trauma plates and screws, CMF, approximation pins and rods, dentures, veneers, dental implants/abutments, impression material, autoclave equipment, dental units, limb lengthening systems, and intra-oral x-ray equipment. Accessories: tunnelers, suture wings, convenience kits, stylets, peel away dilators, cannulas, scalpels, suture, guidewires, sheathes, extension sets, repair kits, luer valves, needle/syringes, blood vacuum tubes, needle safe devices, O2 regulators, radiation therapy patient positioning systems, radiation range compensators, sterilization biological and chemical indicators, and fiber wire docking stations. Hardware/Software: neonatal clinical trial software, firmware, RIS software, image repository software, ECG analyses software, TENS, MIRS, MMA, MDDS, EMC therapy, PACS, stereotactic tracking system, stereotactic software, patient monitors, ventilators, lift beds, TMS (transcranial magnetic stimulator), active tinnitus implants, Holter monitors, phototherapy devices, data fusion software, hyperbaric chambers, autoclave sterilizers, powered muscle stimulators, cryosurgical units, MDM workflow software, Doppler and GPS ultrasound scanners, GPS needle sensors, vascular access needles, RF, nerve block needles, fiber optical lasers, neuron stimulators, and therapeutic massagers, MIMS, viewing monitors, body contouring devices. Reusables: nasopharyngoscope, colonoscope, colposcope, neurological endoscope, sinuscope, arthroscope, and laparoscopes, instruments, tunneler rods, irrigation systems, therapeutic mattresses, OB/GYN scopes, patient cables and electrodes, scooters, vein graft tunneling systems, confocal optical imaging devices, and cannulae, 3DHD endoscopes, IR fluorescence and Indocyanine green endoscopes, measuring microscopes. General Surgery: surgical film, pressure mattresses, cryo-biopsy needle, surgical mesh, plugs, anal fissure drug suppository and delivery plunger, anorectic Nifedipine CTD, red light therapy dermatology lasers, surgical lasers, and Continuous Low Irradiance Photodynamic Therapy (CLIPT) for phototherapy drug activation, collection and transport media, disinfecting swabs and wipes, gastrostomy tubes.

    Chief Regulatory Officer, A Leading Medical Device Consulting Firm in FL

    Bachelor of Science (BS), Werner-Siemens School

    New Smyrna Beach,

    Connecticut

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Related Specialties

What Can a Medical Devices Expert Witness Opine On?

Device Design

Creating functional medical device prototypes.

Regulatory Submission

Preparing documents for regulatory approval.

Quality Assurance Testing

Ensuring device safety and efficacy.

Clinical Evaluation

Assessing device performance in clinical settings.

User Training

Educating users on device operation.

Post-Market Surveillance

Monitoring device performance after launch.

FAQs for Medical Devices Expert Witnesses

What is the role of a medical devices expert witness?

A medical devices expert witness is a qualified specialist who explains device design, safety, and standards in legal cases. They assist by reviewing records, testing devices, writing reports, and testifying to clarify complex technical issues.

What types of cases can a medical device expert witness opine on?

A medical device expert witness opines on product defects, FDA compliance, labeling, adverse events, device failures, recalls, design, testing, manufacturing, and post‑market surveillance.

How can a medical devices expert witness strengthen product liability claims?

A medical devices expert witness strengthens product liability claims by explaining device design, testing, standards compliance, and causation in clear, evidence-based testimony.

What qualifications should attorneys prioritize in a medical devices expert witness?

Attorneys should prioritize a medical devices expert witness with advanced clinical or engineering credentials, device-specific experience, regulatory knowledge, and strong testifying history.

How does a medical devices expert witness evaluate device design compliance?

A medical devices expert witness evaluates device design compliance by reviewing design controls, risk management, testing data, regulatory standards, and documentation against FDA and ISO requirements.

What is Expert Institute’s process for selecting medical devices 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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