medical device

Digital
AI and digitisation

AI is coming and regulators are getting prepared

The UK’s MHRA recently published its guidance on its approach to both regulating the use of AI for drug and medical devices, and how it can utilise the technology to improve its regulating

R&D
2nd Medical Device Software Development Europe 2024
Partner Content

2nd Medical Device Software Development Europe 2024

As device developers of all sizes grapple with the updated transition timeline for EU MDR compliance and the recent EU AI Act approval falls short of expectations, the question looms: how can regul