Abstract:Background:The adverse event report of medical devices is one of the post-market surveillance tools for regulators to monitor device performance, detect potential device-related safety issues, and contribute to benefit-risk assessments of these products. Along with the development of the related technologies and market, the amount of adverse events keeps increasing, which results in the need for efficient tools that help to analyze the adverse events monitoring data and to identify the risk signals. Objective:… Show more
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