We invite you to attend our On-demand webinar on “Nitrosamine Impurity Analysis-Achieving Compliance through Chromeleon CDS for GC-MS” which is brought to you by Thermo Fisher Scientific.
This webinar is talking about –
The pharma industry has been impacted with several costly global recalls after Nitrosamine impurities were discovered in various drug substances such as valsartan and ranitidine by the US FDA & EMA. According to new US FDA and EMA recommendations, manufacturers of Angiotensin-receptor blockers (ARBs) or sartans must ensure that their generic sartans should contain no quantifiable levels of nitrosamine impurities after a certain transition period.
Thermo Scientific™ Chromeleon™ 7.3 Chromatography Data System (CDS), together with world class analytical instrumentation, offers significant productivity advances to the laboratory while enabling you to meet evolving regulatory compliance and data integrity requirements.
Speaker: Manoj M. Soman, Product Manager, Chromeleon
He has 20+ years of experience in pharma quality control and quality assurance. In this webinar he will explain how nitrosoamine impurities can be tested in a compliant system.
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