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Journal of Biopharmaceutical Statistics Volume 13, 2003 - Issue 1
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Original Articles

Examining Outlying Subjects and Outlying Records in Bioequivalence Trials

Wenping Wang Pharsight Corporation, Mountain View, California, USACorrespondence[email protected]
&
Shein-Chung Chow Millennium Pharmaceuticals, Inc., Cambridge, Massachusetts, USA
Pages 43-56 | Published online: 16 Aug 2006

Citations (13)

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Read on this site (3)

Durdu Karasoy & Gulcan Daghan. (2012) Examination of Outliers in Bioequivalence Studies. Klinik Psikofarmakoloji Bülteni-Bulletin of Clinical Psychopharmacology 22:4, pages 307-312.
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Robert Schall, Laszlo Endrenyi & Arne Ring. (2010) Residuals and Outliers in Replicate Design Crossover Studies. Journal of Biopharmaceutical Statistics 20:4, pages 835-849.
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JasonJ. Z. Liao. (2007) A New Approach for Outliers in a Bioavailability/Bioequivalence Study. Journal of Biopharmaceutical Statistics 17:3, pages 393-405.
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Articles from other publishers (10)

Carl Peck, Gregory Campbell, Isaac Yoo, Kairui Feng, Meng Hu & Liang Zhao. (2022) Comparing a Bayesian Approach (BEST) with the Two One-Sided t-Tests (TOSTs) for Bioequivalence Studies. The AAPS Journal 24:5.
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Anders Fuglsang. (2021) Increased Patient’s Risk Associated with the Canadian Bioequivalence Guidance Due to Outlier Removal. Therapeutic Innovation & Regulatory Science 56:1, pages 168-172.
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Divan Aristo Burger, Robert Schall & Sean van der Merwe. (2021) A robust method for the assessment of average bioequivalence in the presence of outliers and skewness. Pharmaceutical Research 38:10, pages 1697-1709.
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Ufuk KARADAVUT & Atilla TAŞKIN. (2017) Determination of Outliers in Growing Quail's Data with Different Sample Size. Harran Tarım ve Gıda Bilimleri Dergisi 21:1, pages 99-111.
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Yufen Huang & Bo-Shiang Ke. (2014) Influence analysis on crossover design experiment in bioequivalence studies. Pharmaceutical Statistics 13:2, pages 110-118.
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Gyu-Jin Jeong & Sang-Gue Park. (2011) On Evaluation of Bioequivalence for Highly Variable Drugs. Korean Journal of Applied Statistics 24:6, pages 1055-1076.
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Gyu-Jin Jeong, Sang-Gue Park & Hwa-Hyoung Woo. (2009) Detecting an Outlier in 2X2 Bioequivalence Trial. Communications for Statistical Applications and Methods 16:5, pages 745-751.
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Rabab Tayyem, Reema Tayyem, Naji Najib, Jaafar Tamimi & Mukhtar Shihabeddin. (2008) Built-in quality systems in regulated contract research organizations (CRO) conducting bioequivalence studies: a regulatory science perspective. Accreditation and Quality Assurance 13:8, pages 473-477.
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V. Luzar-Stiffler & C. Stiffler. (2005) Higher-order crossover design outlier detection. Higher-order crossover design outlier detection.
Timothy Ramsay & Naser Elkum. (2007) A COMPARISON OF FOUR DIFFERENT METHODS FOR OUTLIER DETECTION IN BIOEQUIVALENCE STUDIES. Journal of Biopharmaceutical Statistics 15:1, pages 43-52.
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