As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct adequate, efficient bioequivalence studies. In recent years, there have been significant changes to the statistical models for evaluating bioequivalence. In addition, advances in the analytical technology used to detect drug and metabolite levels have m
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Format PDF ● Seiten 1007 ● ISBN 9781482226386 ● Verlag CRC Press ● Erscheinungsjahr 2014 ● herunterladbar 3 mal ● Währung EUR ● ID 7167477 ● Kopierschutz Adobe DRM
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