Frank Vinluan / medcitynews - The FDA said consolidating safety reporting into a single platform, the Adverse Event Monitoring System (AEMS), will increase transparency and reduce costs. But like the legacy systems it replaces, AEMS reports are unverified so causation and frequency of…
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Thursday, March 12, 2026, 5:23 pm / permalink 20659 / 7 stories in 4 days
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