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Journal of Biopharmaceutical Statistics Volume 29, 2019 - Issue 4: Special Issue: Real Word Experience and Randomized Clinical Trials

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Book Review

Bioequivalence and Statistics in Clinical Pharmacology

by S. Patterson and B. Jones, 2017, Chapman and Hall/CRC: Boca Raton, FL 33487-2742. 434 pp., + xxv, £76.99, Hardback, ISBN 9781584885306

Julie BertrandFaculté de Médecine Bichat, IAME,Paris, France

https://orcid.org/0000-0002-6568-1041

, PhD

Pages 728-729 | Published online: 03 Oct 2017

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https://doi.org/10.1080/10543406.2017.1333942
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Chow, S-C., Liu, J-p. (2017). Design and Analysis of Bioavailability and Bioequivalence Studies. Boca Raton, FL: Chapman and Hall/CRC.
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DA. (2001). Guidance for industry: Statistical approaches to establishing bioequivalence, Technical report, FDA.
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EMA. (2010). Guideline on the investigation of bioequivalence, Technical report, EMA.
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