Pharmaceutical companies conduct bioequivalence studies to demonstrate that a new formulation of a drug product ('Test') is sufficiently similar in rate and extent of absorption to the current formulation ('Reference'). Such similarity permits the efficacy and safety results for the Reference formul
A parametric approach to correspondence analysis
โ Scribed by Carles M. Cuadras; Daniel Cuadras
- Publisher
- Elsevier Science
- Year
- 2006
- Tongue
- English
- Weight
- 142 KB
- Volume
- 417
- Category
- Article
- ISSN
- 0024-3795
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