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

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

The FDA monitors generic drugs after approval using real-world data, patient reports, and AI tools to catch safety issues that clinical trials miss. Learn how FAERS, Sentinel, and MedWatch keep millions of users safe.

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RxStore-365: Your Comprehensive Pharmaceuticals Guide

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