Standalone pieces alongside the course: studies explained, regulatory changes, and tools looked at without endorsement. Each article carries its review date and sources.
Regulation & news
Most AI software that qualifies as a medical device will be a high-risk AI system under the EU AI Act. The 2026 Digital Omnibus moved the start date for those duties to 2 August 2028. Here is what applies already, what is coming, and what developers and hospitals should do now.
Important healthcare-AI studies, explained: what was done, what was found, and what it does and does not show.
Changes in how clinical AI is regulated and governed around the world, dated and sourced.
Vendor-neutral looks at models, libraries and tools used in healthcare AI. Mentions are not endorsements.
A practising physician's view on where AI helps, where it doesn't yet, and what to ask before using it.
Educational content only. This material teaches methods; it is not clinical advice. Code, models and examples here are not validated medical devices and must not be used to make decisions about real patients without proper clinical validation, governance and any required regulatory approval. Examples use synthetic or openly licensed de-identified data only. Never paste identifiable patient information into public AI tools. Mentions of models, tools or vendors are for identification, not endorsement.