https://bookmarkingpage.com/story.php?title=post-market-surveillance-for-medical-devices Post-Market Surveillance for Medical Devices is a critical regulatory and quality management process that ensures medical devices continue to perform safely and effectively after they are released into the market. It involves systematically collecting, analyzing, and evaluating data related to device performance, adverse events, customer feedback, and complaints to identify potential risks and take corrective actions. Tue, 20 Jan 2026 06:01:31 UTC en