We’ll help you retain an industry-leading Medical Devices expert
Average Medical Devices Expert Witnesses Court Fees
Review Fee
Deposition Fee
Court Fee
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
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
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
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
Related Specialties
Find Medical Devices Expert Witnesses In:
Alabama
Arizona
Arkansas
California
Colorado
Connecticut
Delaware
Florida
Georgia
Idaho
Illinois
Indiana
Iowa
Kansas
Kentucky
Louisiana
Maine
Maryland
Massachusetts
Minnesota
Mississippi
Missouri
Nebraska
Nevada
New Hampshire
New Jersey
New Mexico
New York
North Carolina
North Dakota
Ohio
Oklahoma
Oregon
Pennsylvania
Rhode Island
South Carolina
South Dakota
Tennessee
Texas
Utah
Vermont
Virginia
Washington
West Virginia
Wisconsin
Wyoming
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.