What kinds of expert testimony are relevant to a medical device injury case?

In a medical device injury case in California, expert testimony may be necessary to prove several elements of the case. Expert testimony can be offered from medical experts, manufacturing and design experts, engineering experts, and regulatory experts. Medical experts can provide testimony to prove that the device itself caused the plaintiff’s injury. This testimony can describe the injury, the cause of the injury, and the damages suffered. Medical experts can also explain the facts of the injury and help the jury understand the connection between the device and the injury. Expert testimony from manufacturing and design experts can include explanations of how the device works, and what kind of risks were associated with its use. Engineering experts can provide testimony on whether the device was designed safely, and whether the manufacturer followed safe practices when the device was made. Engineering experts can also discuss the possibility of mechanical or electrical failures or flaws in the design of the device. Finally, regulatory experts can provide testimony on the laws and regulations applicable to medical devices, as well as industry standards and guidelines. Regulatory experts can help the jury understand what safety requirements were in place for the device at the time it was made and sold. This testimony can help the jury decide if the manufacturer or seller breached any of the safety standards or regulations. Overall, medical device injury cases require expert testimony to assess the technical and medical details of the device and its use, as well as the relevant safety laws, regulations, and industry standards. This testimony can help the jury make an informed decision in the case.

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What kinds of expert testimony are relevant to a medical device injury case?

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