On Assessment of Bioequivalence for Drugs with Negligible Plasma Levels

Author:

Liu Jen-Pei,Chow Shein-Chung

Publisher

Wiley

Subject

Statistics, Probability and Uncertainty,General Medicine,Statistics and Probability

Reference13 articles.

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2. and , 1987: Statistical Methods in Medical Research. 2nd Ed., Blackwell Scientific Publications, Oxford.

3. The analysis of failure time data in crossover studies

4. 1991: Statistical controversies in design and analysis of bioequivalence trial for pharmaceuticals with negligible blood levels: the metered dose intraler tria l. Presented at the 14th Midwest Biopharmaceutical Statistics Workshop, Muncie, Indiana.

5. The two-period cross-over clinical trial.

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3. References;Crossover Designs;2016-08-12

4. Notes on testing noninferiority in multivariate binary data under the matched-pair design;Statistical Methods in Medical Research;2016-07-11

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