Introduction. In case of methods of impurities determination quite often there are problems connected both with establishment and with check of implementation of the requirement to necessary sensitivity of a chromatographic system.Text. Influence of correction factors and late eluting peaks of impurities on the requirement for the signal-to-noise ratio (S/N) for chromatographic system suitability testing is considered.Conclusion. The recommendations are provided how to detect situations at which the requirement of S/N≥10 is insufficient for reliable detecting peaks of all impurities (related substances) and therewith how to correct concentration of test solution and/or the requirement to S/N for system suitability testing
Multiple testing issues in discriminating compound-related peaks and chromatograms from high frequen...
For the determination of accurate quantity of impurities in the samples authentic impurity standards...
It is necessary to determine the limit of detection when validating any analytical method. For metho...
The article provides answers to urgent questions relating to the acceptable values of disregard limi...
The recommendations of admissible corrections of the chromatographic conditions provided in chapter ...
Introduction. When developing and validating methods of impurity determination, it is important to t...
Chromatography is, in principle, a dilution process. In HPLC analysis, on dis-solving the substances...
The quality of liquid chromatographic methods developed for pharmaceutical applications is strongly ...
Stability indicating assay describes a technique which is used to analyse the stability of drug subs...
Liquid Chromatography - Mass Spectrometry (LC-MS) is a powerful method for sensitive detection and q...
(A) SE-HPLC chromatograms analyzing size variants, (B) SEC-MALS chromatograms analyzing size variant...
The assay of a drug substance (DS) is one of the tests required to confirm the active pharmaceutical...
Liquid Chromatography - Mass Spectrometry (LC-MS) is a powerful method for sensitive detection and q...
Purpose To predict precision and other performance character-istics of chromatographic purity method...
In biopharmaceutical product development and subsequent characterization, there are two classes of i...
Multiple testing issues in discriminating compound-related peaks and chromatograms from high frequen...
For the determination of accurate quantity of impurities in the samples authentic impurity standards...
It is necessary to determine the limit of detection when validating any analytical method. For metho...
The article provides answers to urgent questions relating to the acceptable values of disregard limi...
The recommendations of admissible corrections of the chromatographic conditions provided in chapter ...
Introduction. When developing and validating methods of impurity determination, it is important to t...
Chromatography is, in principle, a dilution process. In HPLC analysis, on dis-solving the substances...
The quality of liquid chromatographic methods developed for pharmaceutical applications is strongly ...
Stability indicating assay describes a technique which is used to analyse the stability of drug subs...
Liquid Chromatography - Mass Spectrometry (LC-MS) is a powerful method for sensitive detection and q...
(A) SE-HPLC chromatograms analyzing size variants, (B) SEC-MALS chromatograms analyzing size variant...
The assay of a drug substance (DS) is one of the tests required to confirm the active pharmaceutical...
Liquid Chromatography - Mass Spectrometry (LC-MS) is a powerful method for sensitive detection and q...
Purpose To predict precision and other performance character-istics of chromatographic purity method...
In biopharmaceutical product development and subsequent characterization, there are two classes of i...
Multiple testing issues in discriminating compound-related peaks and chromatograms from high frequen...
For the determination of accurate quantity of impurities in the samples authentic impurity standards...
It is necessary to determine the limit of detection when validating any analytical method. For metho...