Evaluation of in vivo bioequivalence met
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Jui-Chen Tsai; Ching-Ling Cheng; Yi-Fang Tsai; Hamm-Ming Sheu; Chen-Hsi Chou
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Article
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2004
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John Wiley and Sons
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English
โ 158 KB
The United States Food and Drug Administration recommends pilot dose duration-response and pivotal bioequivalence studies to be conducted using reflectance colorimetry for assessment of the in vivo bioequivalence of topical dermatologic corticosteroids. The major objectives of the present studies we