| Literature DB >> 6644568 |
H Fluehler, A P Grieve, D Mandallaz, J Mau, H A Moser.
Abstract
The statistical methods required for a Bayesian analysis of bioequivalence are outlined and numerically illustrated. The analysis consists of the calculation of the posterior probability, given the experimental results, that the ratio of true means of a new and a standard formulation of a drug with respect to some biological response lies in a given interval. Nomograms helpful for the calculation of these probabilities are provided.Mesh:
Year: 1983 PMID: 6644568 DOI: 10.1002/jps.2600721018
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534