Short description Close the performance gap in your chromatographic analysis by making the most of your GC, LC, IC or SEC data. Contains much valuable know-how for meeting the data quality standards of the FDA, EMEA, and other regulatory agencies.
From the contents EVALUATION AND ESTIMATION OF CHROMATOGRAPHIC DATA Evaluating Chromatograms (Hans-Joachim Kuss and Daniel Stauffer) Integration Parameters (Daniel Stauffer and Hans-Joachim Kuss) Integration Errors (Hans-Joachim Kuss) Simulation of Chromatograms (Uwe Neue) Integration of Asymmetric Peaks (Hans-Joachim Kuss) Deconvolution (Mike Hillebrand) General Interpretation of Analytical Data (Joachim Ermer) Metrological Aspects of Chromatographic Data Evaluation (Ulrich Panne) CHARACTERIZATION OF THE EVALUATION OF DIFFERENT CHROMATOGRAPHIC MODES Evaluation and Estimation of Chromatographic Data in GC (Werner Engewald) Data evaluation in LC-MS (Hartmut Kirchherr) Evaluation of Chromatography Data in Ion Chromatography (Heiko Herrmann and Detlef Jensen) Qualification of GPC/GFC/SEC Data and Results (Daniela Held and Peter Kilz) REQUIREMENTS FOR CHROMATOGRAPHIC DATA ANALYSIS FROM THE VIEWPOINT OF ORGANISATIONS AND PUBLIC AUTHORITIES The Science Behind the Pharmaceutical Regulatory Chromatographic Procedures (Linda Ng) Interpretation of Chromatographic Data According to the Pharmacopoeias-Control of Impurities (Ulrich Rose) Requirements of (Chromatographic) Data in Pharmaceutical Analysis (Joachim Ermer) Evaluation and Valuation of Chromatographic Data (Stavros Kromidas)
