The transition from controlled clinical trials to real-world clinical application introduces a great number of variables that can affect device performance and patient safety. This is where PMCF studies become indispensable, providing a structured approach to gathering real-world evidence (RWE) that supports ongoing assessment of device performance and patient safety.
In this post, we delve into the significance of PMCF studies and how they contribute to collecting real-world. Read the whole article here: Post-Market Clinical Follow-up (PMCF): A Crucial Component of Medical Device Evaluation
For further information, you can contact us at: [email protected]
Or schedule a free 30-minutes meeting here: SCHEDULE A MEETING HERE
