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Post-Market Surveillance: How the FDA Monitors Generic Drugs After Approval
Medications

Post-Market Surveillance: How the FDA Monitors Generic Drugs After Approval

The FDA monitors generic drugs after approval using real-world data, adverse event reports, and AI tools to catch safety issues that clinical trials miss. Learn how FAERS, Sentinel, and inspections keep generics safe.

  • Dec, 21 2025
  • 14

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