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 ...
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 ...
HHS says COVID-19 data reporting system won’t go back to CDC Michael Caputo, HHS assistant secretary, told Texas-based News West 9 that the hospital COVID-19 data reporting system will not be ...
The US Food and Drug Administration (FDA) has announced that starting on 1 October 2026, manufacturers must submit adverse event individual case safety reports (ICSRs) for drugs, biologics, and ...
Opinion
Proactive drug safety surveillance should be at the heart of a new health data research service
The UK’s surveillance system is limited by data that are fragmented, difficult and slow to access, and of variable quality, write Anthony Harnden and Alison Cave The UK is at a pivotal moment for ...
schedule, safety and quality, the framework gave our leaders earlier, clearer risk signals without adding reporting burdens ...
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.
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