Medical Devices Expert Witnesses in Massachusetts
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Biomedical Patent Licensing & Negotiation Expert Witness
Massachusetts
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...
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Biomedical Engineering & Neuroscience Expert Witness
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...
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Medical Devices & Bioengineering and Regulatory Affairs Expert Witness
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...
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Medical Devices Expert Witness FAQs
A medical device expert witness is a professional with extensive knowledge and experience in the field of medical devices. They provide testimony or consultation in legal cases involving these devices.
Medical device experts can handle cases involving product liability, patent infringement, regulatory compliance, failure analysis, and personal injury related to medical devices.
Yes, some experts specialize in specific types of devices such as orthopedic implants, cardiovascular devices, diagnostic equipment, or surgical instruments.
They can analyze the design, manufacturing process, and usage instructions of the device to determine if any negligence occurred that could have led to harm or injury.
An expert in FDA regulations can provide insight into whether a device was compliant with all necessary rules and guidelines at the time of an incident.
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