The Modernization of Cosmetics Regulation Act of 2022 (MoCRA) is bringing sweeping changes to the cosmetics industry. One such change requires a “responsible person” to maintain and submit certain ...
The FDA launched The Adverse Event Monitoring System (AEMS), calling it a major achievement in the agency’s mission to modernize and provide radical transparency into the safety of regulated products.
MedPage Today on MSN
Goodbye FAERS? FDA launches new combined adverse event database
System will replace safety databases monitoring drugs, devices, food, and more ...
The U.S. Food and Drug Administration this week posted a final rule in the Federal Register mandating that device manufacturers and importers submit adverse event reports for medical devices ...
Last month, the US Food and Drug Administration (FDA) announced that it would begin daily publication of adverse event data for drugs and biologics via the FDA Adverse Event Reporting System (FAERS).
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