In this informative podcast on the GCP Mindset channel, expert Martin Schäfer discusses the topic of post-market clinical follow-up (PMCF) studies. As medical technology advances, it’s becoming increasingly important to test products in everyday use to identify any safety concerns that were not detected during pre-market testing. Schäfer explains the different types of PMCF studies and their regulatory requirements, including the challenges of navigating different national regulations. He also offers valuable advice for planning a PMCF study, such as being realistic about timelines and seeking advice to ensure compliance with ethical and regulatory standards. This is a must-watch video for anyone involved in the medical device industry.