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In letters citing these regulations, FDA notes, [c]omponent testing is fundamental to drug product quality and [w]ithout adequate testing, you do not have scientific evidence that your incoming components conform to appropriate specifications before use in the manufacture of drug products. 3 Two issues in particular often arose when FDA cited component testing failures: first, where firms failed to perform adequate identity testing of each component lot used in the manufacture of a product and, second, where manufacturers relied on a suppliers certificate of analysis (COA) without establishing the reliability of the component suppliers test analyses at appropriate intervals

Before human trials can commence, extensive laboratory testing and in some cases, animal studies, are conducted to evaluate the potential safety and effectiveness of the treatment

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