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Statements
24 April 1995
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carry over effects
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washout periods
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cross over designs
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estimating bioavailability
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testing bioequivalence
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pharmacokinetic parameters
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blood concentration time curve
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maximum concentration
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maximum likelihood estimator
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minimum variance unbiased estimator
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mean of individual subject ratios
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ratio of formulation means
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one-sided interval hypotheses
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variance-balanced designs
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Williams designs
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BIB designs
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outliers
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likelihood distance
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intra-subject and inter-subject variabilities
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residual effects
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non-periodic effects
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