Jan 06, 2017
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In this case study, we share how NAPP Pharmaceuticals and its Cambridge, UK facility leveraged Empower Software to make improvements in its Pharmaceuticals QC and Stability laboratories, improving both critical reporting for management as well as sample throughput for product release.
Jan 06, 2017
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In this presentation, studies evaluate methods transfer for a variety of samples and methods, including USP assays. The app note evaluates the same column and method across multiple instruments from different manufacturers.
Jan 06, 2017
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In this application note, we present a robust and quick UPLC method for analysis of methyl, ethyl, and isopropyl esters of benzenesulfonic acid and monitoring potential genotoxic impurities with accurate confirmation and quantitation.
Jan 06, 2017
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This technical note describes a simple workflow and methodology for the screening and characterization of cosmetics, 3D printing media, food and pharmaceutical packaging extractable applications.
Jan 05, 2017
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The United States Pharmacopeia's new chapter 735 permits the use of XRF spectrometry in pharmaceutical testing for elemental impurities. This whitepaper provides background on the new regulations and the XRF technique, and shows how these spectrometers can be applied to the screening and control of elemental impurities.
Dec 16, 2016
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This whitepaper will describe the best practices of risk management and highlight the use of technology-based risk management tools to decrease recall risk in the life sciences.
Nov 22, 2016
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This application notebook is a compilation of key Waters applications in impurities, organized in three distinct sections: pharmaceutical pipeline, application workflow, and trending topics.
Nov 18, 2016
Learn about regulatory and manufacturing considerations when implementing on-dose verification technologies for branded solid oral dosage form drugs and how this technology can provide customized business intelligence at the dosage level without relying exclusively on product packaging. Industry experts will review FDA’s guidance on physical-chemical identifiers in solid dosage drug forms for the purpose of product security and will share real-world testing and piloting completed in manufacturing environments.
Nov 16, 2016
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TruTag Technologies and WuXi AppTec collaborated on the application of TruTag's microtag on-dose authentication solution for SODF drugs. Discover the effectiveness of this application and the results of these studies.
Nov 04, 2016
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This application notebook is a compilation of key applications that analyze biotherapeutics at multiple levels of structure, including intact protein, peptide digest, and released glycan.