Power of the two one-sided tests procedure in bioequivalence-Reference-Cited by-同舟云学术

Power of the two one-sided tests procedure in bioequivalence

Published:1990-04 Issue:2 Volume:18 Page:137-144
ISSN:0090-466X
Container-title:Journal of Pharmacokinetics and Biopharmaceutics
language:en
Short-container-title:Journal of Pharmacokinetics and Biopharmaceutics

Author:

Phillips Kem F.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/content/pdf/10.1007/BF01063556.pdf

Reference7 articles.

1. Bioequivalence Task Force. Report on recommendations from the bioequivalence hearing conducted by the Food and Drug Administration, September 29–October 1, 1986.

2. D. J. Schuirmann. A comparison of the two one-sided tests procedure and the power approach for assessing the equivalence of average bioavailability.J. Pharmacokin. Biopharm. 15:657–680 (1987).

3. W. W. Hauck and S. Anderson. A new statistical procedure for testing equivalence in two-group comparative bioavailability trials.J. Pharmacokin, Biopharm. 12:83–91 (1984).

4. R. E. Odeh and D. B. Owen.Tables for Normal Tolerance Limits, Sampling Plans, and Screening, Marcel Dekker, New York, 1980.

5. D. B. Owen, A special case of a noncentralt-distribution.Biometrika 52:437–446 (1965).

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