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PAT In-Depth Focus 2015

6 January 2016 | By

Featuring an overview of process analytical control; Beyond API monitoring: in-line Raman spectroscopy for process control; Monitoring, understanding and assessing pharmaceutical process and product quality; and a PAT roundtable...

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Use of the ‘purge tool’ in assessing mutagenic impurities

6 January 2016 | By Dave Elder, GlaxoSmithKline and JPAG

The International Conference on Harmonization M7 text provides guidance on establishing acceptable levels of mutagenic impurities (MIs) . It also outlines the safety and quality risk management processes that manufacturers need to undertake to control MIs that may potentially affect the drug substance or drug product. Over the past decade,…

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CI Precision announces new release of its MES

16 November 2015 | By CI Precision

CI Precision, global supplier of MES and weight sorting solutions, announces the release of version 6 of Ci-DMS, their manufacturing execution system (MES) which has gained established use in pharmaceuticals production...