Consolidating adverse event databases is a smart move, but without public education, real-time transparency risks becoming ...

When safety concerns emerged for an FDA-regulated product, the suspected problem could be reported to one of seven online databases. The agency is now consolidating this reporting into a single online ...

ThinkTrends agentic Document AI platform has been deployed at the U.S. Federal Health Agency as part of its new nationwide Adverse Event Monitoring System (AEMS), a major modernization initiative to ...

FIRST ON FOX: The Food and Drug Administration (FDA) rolled out a new platform, backed by artificial intelligence, that will streamline publicly accessible reporting of negative or unexpected health ...

Oshkosh has been granted a patent for a vehicle with a thermal event monitoring system that can detect fires or overheating components and reroute the vehicle to a safe location such as a service ...

WASHINGTON - The Food and Drug Administration has launched what it is describing as a "unified dashboard" for identifying and monitoring unexpected side effects or injuries caused by approved medical ...

The US Food and Drug Administration (FDA) announced it is unifying its various adverse reporting systems into a single system called the Adverse Event Monitoring System (AEMS). The agency said the ...

Driver monitoring systems, or DMS for short, are a sophisticated new type of auto technology designed to provide real-time assessments of a driver’s fitness to operate their vehicle. Specifically, ...