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...
Specialties:
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...
Specialties:
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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A biomedical expert witness is a professional with extensive knowledge in the field of biomedical science. They provide testimony or informed opinions in legal cases involving medical devices, pharmaceuticals, and healthcare technology.
Biomedical expert witnesses are crucial in cases involving medical device failures, patent disputes, pharmaceutical litigation, personal injury claims related to medical equipment, and more.
Subspecialties include biomechanics, biomaterials, bioinformatics, medical imaging, genetic engineering, and regenerative medicine. Each has unique applications in legal proceedings.
They can analyze the device's design, manufacturing process, and usage to determine if there were any flaws or negligence that could have led to its failure.
Understanding FDA regulations is key as they govern the approval and monitoring of medical devices and pharmaceuticals. This knowledge can help identify non-compliance or malpractice.
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