Enhanced monitoring of biopharmaceutical product purity using liquid chromatography–mass spectrometry
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry
Reference33 articles.
1. International Conference on Harmonization (ICH) – Guidance for Industry: Q3A(R2) Impurities in New Drug Substances, 2006.
2. International Conference on Harmonization (ICH) – Guidance for Industry: Q3B(R2) Impurities in New Drug Products, 2006.
3. Peak purity determination with principal component analysis of high-performance liquid chromatography–diode array detection data
4. Current Developments in LC-MS for Pharmaceutical Analysis
5. An automatic peak finding method for LC-MS data using Gaussian second derivative filtering
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