AI was a key theme at OCT Medical Devices 2025, yet human sensibility appears to be the true differentiator in clinical trial ...

An important facet of AI regulation is where in the supply chain AI should be regulated—specifically, whether to regulate the ...

The FDA’s framework for AI regulation, while robust for premarket evaluation, would benefit from more specific mechanisms for continuous monitoring of AI performance in diverse real-world settings.

Countries and economic blocs around the world are at different stages of regulating artificial intelligence, from a relative ...

In the EU, the AI Act has been approved, carrying significant implications for medical device, technology, and pharmaceutical firms. In the US, ...

On 21 st January 2025, the EU Council approved the EU Health Data Space Regulation (the " EHDSR "). This will come into force ...

Medical Device Market Size was estimated at USD 335428.32 million in 2024 and it is expected to grow from USD 354883.17 million in 2025 to USD 397243.44 million by 2033. The Market CAGR (growth rate) ...

Here are some key points about regulation in major jurisdictions, ahead of the Paris AI summit on February 10-11: Returning President Donald Trump last month rescinded Joe Biden's October 2023 ...