Rob Reid

2025 in MedTech: a year of innovation, global leadership and regulatory milestones

Posted by: , Posted on: - Categories: AI Airlock, Diagnostics, Health Institution Exemption, IMDRF, IVD, Med Tech Regulations, Medical Devices, Post-Market Surveillance, Pre-market statutory instrument, Uncategorized

Rob Reid, MHRA deputy director of innovation devices, at AI Airlock Connect, October 2025 As the end of 2025 rapidly approaches, I find myself searching out those articles and lists that reflect on key moments across the year. Whether it …

MedTech regulatory reform and the importance of partnerships

Posted by: , Posted on: - Categories: Med Tech Regulations

Medical technologies will play a critical role in delivering the government’s 10 Year Health Plan and its three shifts: hospital to community; analogue to digital; and sickness to prevention. Risk-proportionate regulation, which ensures patient safety whilst supporting innovation and access, …