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Chapter and Verse: USP 621 and You

By February 23, 2015

In August 2014, the United States Pharmacopeia and the National Formulary (USP-NF) put into effect new guidelines to “allowable adjustments” in its Chapter <621> (USP37-NF32 S1). And as of August 1, 2016 when USP 39… Read more >

Categories: General, Pharmaceutical, Technologies
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Webinar discusses new purity method, 40X increase in productivity

By October 30, 2014

Webinar: QbD Development of a Purity Method Chromicent GmbH (Berlin, Germany) managing directors Alexander Schmidt and Mijo Stanic are experts in the development and validation of analytical methods according to the latest quality-by-design approaches. The… Read more >

Categories: Pharmaceutical
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