The FDA has launched a unified Adverse Event Monitoring System (AEMS) to consolidate safety reports across all regulated products and is piloting real-time clinical trial monitoring. The move replaces ...
Despite decades of patient safety initiatives, preventable harm remains prevalent in health care. This article posits that a ...
A recent Office of Inspector General (OIG) study revealed a startling statistic: U.S. hospitals are missing approximately half of all patient harm events. While this figure undoubtedly represents a ...
Unfortunately, this book can't be printed from the OpenBook. If you need to print pages from this book, we recommend downloading it as a PDF. Visit NAP.edu/10766 to get more information about this ...
New research from Verdantix highlights a growing shift toward integrated AI systems to manage complex workplace safety risks.
With former director of the FDA’s Center for Biologics Evaluation and Research Peter Marks, M.D., Ph.D., out of the picture, HHS secretary Robert F. Kennedy Jr. (RFK Jr.) appears to be setting his ...
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 ...
Construction organizations put enormous effort into safety. Walk any job and you’ll see it in motion: inductions, JHAs, permit sign-ons, PTPs, inspections, observations, etc. But anyone with site ...
Daniel Payne reports on how the health industry and Washington influence and impact each other. He joined STAT in 2025 after covering health care at POLITICO. You can reach Daniel on Signal at danielp ...
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