Bioequivalence is the attribute of a medication with respect to a reference. Both have different manufacturing origins but contain the same active ingredient and are similar in quantity and speed of drug absorption when administered orally, within reasonable limits established by statistical procedures.

The purpose of bioequivalence is to demonstrate that two drugs containing the same substance at the same dose are equivalent in terms of quality, efficacy and safety for the recipient patient.

At Asofarma Central America and Caribbean we consider that Bioequivalence is a demonstration of quality and our laboratory is making the necessary studies on the products that require it.