Post-market surveillance remains a critical pillar of medical device regulation, ensuring that products placed on the market continue to meet safety and performance requirements throughout their lifecycle. In Ireland, the Health Products Regulatory Authority (HPRA) regularly publishes summaries of Field Safety Notices affecting the Irish market, offering valuable insight into ongoing safety monitoring activities. The latest summary covering February 2026 highlights the conti

After the United Kingdom’s exit from the European Union, the UK and EU established the Windsor Framework, aiming to restore the smooth...