Tag: pharmacovigilance

MedWatch Reporting for Generics: How Safety Data is Collected

MedWatch Reporting for Generics: How Safety Data is Collected

20 March 2026

MedWatch is the FDA's system for collecting safety data on generic drugs, but reporting gaps make it hard to track which manufacturer caused a reaction. Learn how reports are submitted, why they often miss key details, and how the system is evolving to catch dangerous patterns.

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How to Track Post-Marketing Studies for Drug Safety

How to Track Post-Marketing Studies for Drug Safety

15 March 2026

Learn how to track post-marketing studies for drug safety using FDA systems like FAERS and Sentinel. Understand reporting requirements, signal detection, and best practices to ensure ongoing drug safety after approval.

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