对卡尔·M·梅茨勒所著《生物利用度研究中方差评估：对麦克纳马拉等人文章的评论》的回复 - Suppr

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Reply to "Assessment of Variance in Bioavailability Studies: comments on the article by McNamara et al." by Carl M. Metzler.

作者信息

Skelly J P, Shah V P, Schuirmann D J

出版信息

Pharm Res. 1988 May;5(5):322. doi: 10.1023/a:1015991007536.

DOI:10.1023/a:1015991007536

PMID:3244644

Abstract

摘要

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引用本文的文献

Review of methods and criteria for the evaluation of bioequivalence studies.生物等效性研究评估方法与标准综述

Eur J Clin Pharmacol. 1990;38(1):5-10. doi: 10.1007/BF00314794.

本文引用的文献

Statistical simulation study of new proposed uniformity requirement for bioequivalency studies.

J Pharm Sci. 1981 Jun;70(6):673-5. doi: 10.1002/jps.2600700625.

Influence of tablet dissolution on furosemide bioavailability: a bioequivalence study.

Pharm Res. 1987 Apr;4(2):150-3. doi: 10.1023/a:1016427321532.

Assessment of variance in bioavailability studies: comments on the article by McNamara et al.生物利用度研究中的方差评估：对麦克纳马拉等人文章的评论

Pharm Res. 1987 Dec;4(6):536. doi: 10.1023/a:1016448110088.

A comparison of the two one-sided tests procedure and the power approach for assessing the equivalence of average bioavailability.两种单侧检验方法与评估平均生物利用度等效性的效能法的比较。

J Pharmacokinet Biopharm. 1987 Dec;15(6):657-80. doi: 10.1007/BF01068419.

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