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)|
|Number of pages||7|
|Journal||International Journal of Clinical Pharmacology Therapy and Toxicology|
|State||Published - Jan 1 1994|
All Science Journal Classification (ASJC) codes
- Pharmacology (medical)