The Expert’s Guide to Pharmaceutical Impurity Analysis
Download this eBook, produced in collaboration with Agilent, to discover the latest regulations, tools, and techniques in pharmaceutical impurity analysis.
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Download this eBook, produced in collaboration with Agilent, to discover the latest regulations, tools, and techniques in pharmaceutical impurity analysis.
Learn practical strategies to decrease uncertainty in comprehensive extractables and leachables analysis by LC/MS.
In extractables studies, LC/UV/MS is commonly used to detect and annotate the non-volatile fraction of compounds. In this presentation, we discuss the challenges associated with these analyses...
Discover the benefits of synthetic carbon separation media in both liquid and gas purifications and how they bring value to a range of LPLC applications.
An LC-UV/MS method is presented using a corresponding E&L certified reference material (CRM) mix for LC screening containing 21 extractables that can typically be found.
Introducing a series of new reference materials for E&L testing, including a toxic degradation product of Irganox 1010.
This work presents a novel tool to study E&L compounds using a high-resolution accurate mass GC/Q-TOF equipped with a low-energy EI capable ion source.
Background to E&Ls, the single use system, model device used, extraction conditions, qualitative results, mass spectroscopy software and method sensitivity
Analytical trends and novel applications of chromatography and mass spectrometry to the characterization of biotheapeutics and biosimilars
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