Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10554013 | Journal of Pharmaceutical and Biomedical Analysis | 2005 | 12 Pages |
Abstract
If the analytical system is demonstrated to be stable, i.e. under statistical control, a major variability contribution in LC originating from the standard preparation and analysis can be reduced. A concept of quantification by pre-determined calibration parameters instead of the classical approach of simultaneous calibration is described.
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Joachim Ermer, Hans-Joachim Ploss,