After massive developments in large language models in the past two years, the next wave of AI will turn medical devices into ...
As the FDA continues to develop and solidify its guidance and regulations on AI, medical device manufacturers should prepare ...
With the usage of AI in medical devices, ethical concerns center on patient health data, safety, and privacy, which adds an ...
Dr. Michelle Tarver, a veteran of the Food and Drug Administration (FDA), has taken charge of the FDA’s device division at a ...
Christina JewettThere are now artificial intelligence programs that scan MRIs for signs of cancer, Apple AirPods that work as ...
NPR's Ayesha Rascoe speaks with U.S. FDA Commissioner Robert Califf about the agency's process for regulating artificial intelligence in healthcare.
Over the past decade, FDA approvals of artificial intelligence and machine learning (AI/ML)–enabled medical devices have surged. They reached a ...
The new director overseeing medical devices will confront criticisms about hasty approvals as she ushers in revolutionary technology. By Christina Jewett There are now artificial intelligence ...
The Pharmaceutical Automation and Digitalisation Congress (AUTOMA+) is providing a valuable opportunity to access innovations considering AI implementation in pharmaceutical devices during the ...
The EU AI Act, which went into force on August 1, 2024, introduces specific rules for artificial intelligence (AI) systems, especially those ...
The U.S. Food and Drug Administration announced Tuesday that it has appointed Dr. Michelle Tarver to head its divis ...
Quantiphi Global Head of Healthcare and Life Sciences Barinder Marhok said the partnership marries DDReg’s expertise in ...