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 ...

Healthcare leaders have a responsibility to accelerate deployment of technologies that can detect unreported safety events, writes Press Ganey Chief Safety and Transformation Officer Tejal Gandhi, M.D ...

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 ...

Omega Systems, a provider of managed IT and security services, released new research that reveals the growing impact of cybersecurity challenges on leading healthcare organizations and patient safety.