Biostatistical methodology in clinical trials — a European guideline

Author:

Lewis John A.,Jones David R.,Röhmel Joachim

Publisher

Wiley

Subject

Statistics and Probability,Epidemiology

Reference7 articles.

1. and (eds), Proceedings of the First International Conference on Harmonisation, Queen's University of Belfast, 1992.

2. D'Arcy, P. F. and Harron, D. W. G. (eds), Proceedings of the Second International Conference on Harmonisation, Queen's University of Belfast, 1992.

3. Food and Drug Administration. Guideline for the Format and Content of the Clinical and Statistical Sections of New Drug Applications, FDA, US Department of Health and Human Services, Rockville, MA, USA, 1988.

4. Good Clinical Practice for Trials on Medicinal Products in the European Community: CPMP Working Party on Efficacy of Medicinal Products

5. THE CASE FOR CROSS-OVER TRIALS IN PHASE III

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