{"id":1203,"date":"2023-10-05T10:35:42","date_gmt":"2023-10-05T08:35:42","guid":{"rendered":"https:\/\/www.bayoomed.com\/operations\/post-market-surveillance\/"},"modified":"2024-07-01T17:43:25","modified_gmt":"2024-07-01T15:43:25","slug":"post-market-surveillance","status":"publish","type":"operations","link":"https:\/\/www.bayoomed.com\/en\/operations\/post-market-surveillance\/","title":{"rendered":"Post-Market Surveillance"},"content":{"rendered":"

Post-market surveillance: What happens after the product is placed on the market?<\/h2><\/h2><\/div>
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Post-Market Surveillance (PMS), i.e. the monitoring and review of approved medical devices, refers to the process after they have been placed on the market. This structured process aims to derive possible corrective measures for the product based on market behavior.<\/p>\n

 <\/p><\/p>\n<\/div><\/div><\/div><\/div><\/div>

This is the focus of post-market surveillance<\/h3><\/h3><\/div><\/div><\/div>
Identify risks<\/h5><\/h5><\/div><\/div><\/div>
Determine effectiveness compared to other products<\/span><\/h5><\/h5><\/div><\/div><\/div>
Initiate significant measures quickly<\/h5><\/h5><\/div><\/div><\/div>
Uncover existing security problems<\/h5><\/h5><\/div><\/div><\/div>
Update risk management<\/h5><\/h5><\/div><\/div><\/div><\/div><\/div>

This is how we proceed for your Post-Market Surveillance<\/h3><\/h3><\/div>