Software and Artificial Intelligence (AI) as a Medical Device

The MHRA's authoritative guidance on when software and AI applications qualify as medical devices and how they are regulated in the UK, including intended-purpose statements and adverse incident reporting. Essential reading for clinicians accountable for the safe deployment of AI-enabled software. Provider: MHRA · Audience: Clinical safety officers, medical directors, clinical informaticians and anyone procuring or deploying AI tools · Listed cost: Free