FDA seeks input on proposed regulatory approach to GenAI-based medtech
Feedback on the FDA's discussion paper around regulation for GenAI-enabled medical devices is open to interested parties until October 2026.
Feedback on the FDA's discussion paper around regulation for GenAI-enabled medical devices is open to interested parties until October 2026.
With regulatory conditions tightening around climate impact and environmental persistence of medical propellants, HFA-152a is a practical route to maintain clinical performance, patient outcomes and supply continuity of inhalers. However,...
The medical devices industry continues to be a hotbed of patent innovation. Activity is driven by increased need for homecare,...
UK government champions healthtech through new NHS access programme
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The increased importance of safety for wearable devices
What does the EU Data Act mean for businesses?