What does it mean for a product to have FDA (Federal Drug Administration) approval?

In the United States, prescription drugs and biologics are required to undergo rigorous laboratory, animal, and human clinical testing before they can be put on the market. The Food and Drug Administration (FDA) reviews the results of these studies to: verify the identity, potency, purity, and stability of the "ingredients," and demonstrate that the drug is safe and effective for its intended use.

We thought you might find these product(s) useful:


• Hepatitis C Testing - Hepatitis C Home Test Kit

[Related Link]

Keywords: hepatitis c hepatitis c test kit hepatitis c results

Back To Hepatitis C FAQ

Home My Account Order Status Contact Us About TestCountry Sales & Partners Corporate Accounts Affiliate Program

Information TestCountry Resources Health & Drug Testing Information Center Drug Slang & Street Name Search Local Drug Testing Centers Support Store Policies FAQ