| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1225088 | Journal of Pharmaceutical and Biomedical Analysis | 2006 | 6 Pages |
Abstract
Simple statistical, mathematical, and chemical arguments are presented that will justify performing all stability studies using a different approach than is currently practiced in the pharmaceutical and IVD industries. The use of multi time point stability studies is in most cases a waste of resources that could be better spent on endpoint studies at less cost and a significant increase in the quality of the data.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Karl De Vore,