The European Parliament adopted the EU AI Act in plenary on 13 March. Experts say the wider success of the EU’s approach to AI is now in the hands of the EU AI Office.
The European Parliament has adopted the EU AI Act. However, “implementation is going to be key,” Dragos Tudorache, co-rapporteur on the AI Act European Parliament plenary vote, said in the press conference.
In a separate interview Stephen Gilbert, medical device regulatory professor at the Else Kröner Fresenius Center for Digital Health, told Medtech Insight, “the entire success of the
The intricate assembly of medical devices, often involving over 1,000 globally sourced components, faces severe disruption due to new US tariffs. These barriers could halt production and devastate small and medium-sized enterprises (SMEs), MedTech Europe’s CEO, Oliver Bisazza, warns in an interview with Medtech Insight.
Manufacturers of medical products would be foolish to think that recent upheavals at the US FDA will result in a lack of inspections in the coming years. A panel of experts discussed the current state of inspections during a webinar hosted by the Food and Drug Law Institute.
Its move comes as the Swiss recognize the need to ensure adequate supplies on medical devices in its country.
Back-to-back meetings at LSX? No time to attend the innovator showcase? Here is what you might have missed from medtech innovators at the LSX World Congress Europe on 29 April.
