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The Drug Regulator of these countries ( similar to our US Federal Drugs Authority ) allows the Generic Manufacturer company to produce and market its Generic Medicine only after it has conducted BE/BA studies which successfully prove the medicines efficacy as being similar to the compared Brand medicine i.e
Subjects were divided by LH level similar to the first study, this time with 16 patients in the low LH group and 8 in the higher LH group
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