Post Market Surveillance: Why Continuous Monitoring Matters for Medical Devices

Health

Post Market Surveillance: Why Continuous Monitoring Matters for Medical Devices

Launching a medical device into the market is only one step in its regulatory journey. Once the product reaches healthcare professionals and patients, manufacturers are responsible for continuously monitoring its performance, identifying potential risks, and ensuring it continues to meet safety and effectiveness requirements. This ongoing process has become a central requirement under the European Medical Device Regulation (EU MDR). An effective post market surveillance system...