Generative AI chatbot for doctors called 'Prof. Valmed' earns E.U. approval. In the U.S., FDA is yet to issue guidelines on ...

Brazil is experiencing a regulatory revolution that is fundamentally transforming its medical device clinical trial landscape ...

Results show that body fat analysis did indeed predict people’s risk of death from any cause and, specifically, for heart ...

The Food and Drug Administration has published final guidance for the cybersecurity of premarket medical devices. The new ...

As devices come onto the market that have to follow the new FDA guidance of SBOMs and patching, backdoors may become easier ...

Key Takeaways Zero Trust is a fundamental shift in how we think about protecting our networks. If you’ve been in the industry ...

There is not much to like about Apple stock today. Its key product is seeing slowing growth, the profitable services segment ...

A summary of preclinical evaluation methods for neuroendovascular devices, including in vitro techniques, 3D-printed vascular models, in silico simulations, and in vivo models.

Most cases are subclinical, but given the newness of the therapy, it’s necessary to keep tabs on the issue going forward.

A landmark reform of how medical devices are regulated in Great Britain has taken effect, as part of the Medicines and Healthcar ...