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When it comes to ensuring the safety and effectiveness of medications, the U.S. Food and Drug Administration (FDA) plays a crucial role. This post outlines the journey a drug takes from the lab to the market, and how generic medicines fit into this system.

🧪 What Is the FDA’s Role?
The FDA evaluates drugs for their safety, efficacy, and overall quality before they reach consumers.

📋 Phases of Drug Approval:

Preclinical Testing

Clinical Trials

New Drug Application (NDA)

Post-Market Surveillance

💊 What About Generic Drugs?
Generic medicines go through an abbreviated approval process, requiring them to prove bioequivalence to brand-name drugs. This ensures that they’re just as safe and effective—at a fraction of the cost.

🌍 At Generic Medicine Store, we’re committed to offering FDA-approved generic medicines to our global customers at fair prices. We aim to make quality healthcare accessible and affordable worldwide.