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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Biçim PDF ● Sayfalar 1007 ● ISBN 9781482226386 ● Yayımcı CRC Press ● Yayınlanan 2014 ● İndirilebilir 3 kez ● Döviz EUR ● Kimlik 7167477 ● Kopya koruma Adobe DRM
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