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AI and Product Safety Standards Under the EU AI Act

For the EU’s Artificial Intelligence Act to set a global benchmark for AI regulation, the resulting standards need to balance detail and legal clarity with flexibility to adapt to the emerging technologies. Read More..

Identifying Root Causes: Challenges and Trends in Medical Device Recalls
From software glitches to manufacturing flaws, understanding the causes of medical devices issues is critical for improving patient safety and refining regulations. Read More..