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Problems with How Generics are Ap

Posted 11-27-19 at 09:10 PM by wonderboy
1. When a generic firm resolves to submit a application for a generic medication, it is the firm, not the FDA, that conducts clinical tests to confirm that their product is bioequivalent
to the brand name drug.


PROBLEM #1: POOR EXTERNAL AND
INTERNAL VALIDITY


External validity is the degree to which findings from research, tests, and statistical analysis can be accepted as reliable to a broad array of the population.

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