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) |
|---|---|
| Pages (from-to) | 26-32 |
| Number of pages | 7 |
| Journal | International Journal of Clinical Pharmacology Therapy and Toxicology |
| Volume | 32 |
| Issue number | 1 |
| Publication status | Published - Jan 1 1994 |
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All Science Journal Classification (ASJC) codes
- Toxicology
- Pharmacology (medical)