Postmarketing surveillance (PMS) (also post market surveillance) is the practice of monitoring the safety of a medical device by the OEM after it has been released on the market. Postmarketing surveillance uses a number of approaches to monitor the safety of medical devices, including reporting databases, event monitoring, electronic health records, patient registries and record linkage between health databases. These safety data records are reviewed to highlight potential safety concerns in a process known as data mining.
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