Ensuring Patient Safety and Innovation Through Effective Post Market Clinical Follow Up and Clinical Investigation Medical Devices The primary goal of PMCF is to confirm the safety and performance of the device over time. It helps identify previously unknown risks, monitor known side effects, and ensure that the device continues to meet regulatory standards. By collecting real-world evidence, manufacturers can make informed decisions about product improvements and risk management. https://articlescad.com/ensuring-patient-safety-and-innovation-through-effective-post-market-clinical-follow-up-and-clinical-214671.html