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Medical Device Forensic Investigation
The SMDA law of 1990 requires all users of medical devices to have a plan that addresses incidents resulting from medical equipment use or failures that result in a serious injury or illness or death to an individual. The law requires that each incident be reviewed, investigated and reported on a timely basis to the FDA. In the event of such an issue, CEC can provide a full investigation of the event and offer a detailed report on the findings and participation in litigation on your behalf. Clinical Engineering has participated in numerous expert testimonies and insurance investigations.
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