FDA launches new AI-powered system to track drug and vaccine side effects nationwide

FDA launches new AI-powered system to track drug and vaccine side effects in real time, replacing outdated databases and ...
UPI

FDA to provide daily updates on adverse events

The U.S. Food and Drug Administration is now providing real-time, daily publication updates on adverse event data from its reporting system. In an effort to modernize and provide transparency on ...
RAPS

FDA consolidates adverse events reporting systems

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 ...
Regulatory Affairs Professionals Society

FDA sets October deadline for new safety reporting format

The US Food and Drug Administration (FDA) has announced that starting on 1 October 2026, manufacturers must submit adverse ...
Healio

FDA begins daily reporting of adverse event data

Please provide your email address to receive an email when new articles are posted on . The FDA Adverse Event Reporting System will now host daily publications, instead of quarterly. The agency’s goal ...
FiercePharma

FDA rolls out new streamlined adverse event monitoring system, eyes $120M in savings

It’s out with the old, in with the new at the FDA as the agency is unveiling a new adverse events monitoring system that joins several reporting systems into one unified platform, an effort that’s ...
Yahoo

FDA to provide daily updates on adverse events

Add Yahoo as a preferred source to see more of our stories on Google. The FDA announced it will now update its Adverse Event Reporting System every day, instead of once per quarter. Photo courtesy FDA ...