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On sample size calculation in bioequivalence trials on sample size calculation in bioequivalence trials.

Based on the Likelihood. Journal of Biopharmaceutical Statistics, v. M e Singer, J. A dashed line in the chart below indicates an approximate limit relationship between two distribution families. Livraria Atheneu – 1a.

Estatistics designs balanced for the estimation of residual effects of treatment. Journal of Pharmaceutical Statistics ; 4: Here is the GNU version in pdf, and here is the source”. SticiGui — Philip B.

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Chapman and Hall, London, UK, Briefly stated, the FDL permits you to do whatever you like with a work, as long as you don’t prevent anyone else from doing what they like with it. Cambridge University Press, 2a. IRT requires stronger assumptions than classical test theory we will cover these in a moment. Sample sizes for clinical trials with Normal data. Item calibration and ability estimation, II.

Teoria da Resposta ao Item: Introduction to the Theory of Statistics, 3rd. Sample size calculation for bioequivalence studies with high-order crossover designs.