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Published in 2018 at "FARMACIA"
DOI: 10.31925/farmacia.2018.6.2
Abstract: This paper presents an ethical approach of the clinical studies, biostatistical and legislative aspects for testing generics and biosimilars and the valuation of the obtained results in clinical practice and health politics. Both generics and…
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Keywords:
bioequivalence;
clinical studies;
biostatistic legislativ;
case ... See more keywords