FDA has granted breakthrough designation to two devices that use generative AI to interpret chest X-rays and draft the ...

The investigational First Read tool analyzes chest X-rays and drafts preliminary report text for radiologist review and aims to relieve imaging demand strains.

The US Food and Drug Administration (FDA) announced plans to implement AI tools throughout the agency to assist in conducting scientific reviews following the successful completion of a pilot program ...

Health officials launch initiative to boost domestic clinical trials and speed new drug development ...

“I don’t want to get political … ” Alan Minsk, an attorney, was forced to say several times during a panel discussion on the Food and Drug Administration’s use of artificial intelligence, held at the ...

The U.S. Food and Drug Administration seeks to accelerate clinical trials of new medicines by using artificial intelligence to streamline the laborious process of collecting and submitting study data.

FDA proof-of-concept trials with AstraZeneca and Amgen validate continuous data transmission and signal detection, setting ...

The US Food and Drug Administration (FDA) has issued a warning letter to Purolea Cosmetics Lab for several violations of Good Manufacturing Practices (GMP). Notably, the warning letter calls the ...

Artificial intelligence has already made its mark in commercial industries, and there's a good argument to be made that AI is ...