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Diagnostics

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

Rob Reid, 22 December 2025 - 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 …

Emerging Roadmap and transition provisions

Laura Squire, 1 November 2024 - Diagnostics, Med Tech Regulations

A lot has happened in the month since my last blog, including the launch of the national conversation about the NHS and Budget announcement of additional funding for Life Sciences. This has highlighted the vital role of diagnostics and Med …

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