Abstract
This is the consideration of sample sizes for assessing individual bioequivalence based on the use of tolerance intervals. The sample size procedures discussed include a direct distribution-free method, indirect parametric method and a direct parametric method. Design considerations are discussed based on the results of the direct parametric method. Tables are provided for easy access of results.
Original language | English (US) |
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Pages (from-to) | 26-32 |
Number of pages | 7 |
Journal | International Journal of Clinical Pharmacology Therapy and Toxicology |
Volume | 32 |
Issue number | 1 |
State | Published - Jan 1 1994 |
All Science Journal Classification (ASJC) codes
- Toxicology
- Pharmacology (medical)