Post-market clinical follow-up (PMCF) has become significantly more rigorous under the EU MDR to ensure enhanced patient safety following a device’s entry onto the market.

In the 5-minute guide below, our Clinical Consultant Dr. Martina Hersberger and Head of Clinical Dr. Sarah Bosshard share an overview of PMCF and its requirements, along with important advice on the essential do’s and don’ts.

Do you have a PMCF challenge? Our Clinical team is ready and happy to help – simply get in touch to start the conversation.