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3 q&more articles about the topic uhplcrss
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Smart sample preparation improves selectivity of analytical procedures for biopharmaceuticals and other drug products
Impurity testing is an essential part of pharmaceutical quality control because toxicity and content of impurities contained in drug products can impair patient safety. This requires suitable, validated analytical methods.
ICH Linearity Studies using Automated Standard Preparation and UHPLC
According to the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), it is necessary to test analytical methods for their linearity as part of a method validation study. The typical process for this is to prepare standards ...
Nano-, micro-, and two-dimensional HPLC are already proving their worth
A major topic during the HTC conference held in Bruges, which is focused on issues relating to hyphenation processes involving HPLC and innovative detection techniques, was the discussion concerning system volumes of modern UHPLC systems. It is again clear, according to many experts at least, ...
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The q&more concept is to increase the visibility of recent research and innovative solutions, and support the exchange of knowledge. In the broad spectrum of subjects covered, the focus is on achieving maximum quality in highly innovative sectors. As a modern knowledge platform, q&more offers market participants one-of-a-kind networking opportunities. Cutting-edge research is presented by authors of international repute. Attractively presented in a high-quality context, and published in German and English, the original articles introduce new concepts and highlight unconventional solution strategies.
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