Build your pharma development and manufacturing knowledge base with the latest whitepapers, application notes, posters, and other educational resources from bio/pharma industry suppliers.

Developing Safe and Effective Drugs Application Notebook

In this compilation of application notes, we revisit the last decade of developments in impurity analysis and recognize the changing regulatory requirements and future challenges.

Coupling Mass Detection with UV to Improve Method Sensitivity for Esters of Benzenesulfonic Acid in Analysis of Genotoxic Impurities

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.

Screening Workflow for Extractables Testing Using a Scientific Information System:

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.

The Impact of LC Instrument Characteristics on Method Migration and Method Transfer

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.

Improving quality control and stability testing efficiency with standardized chromatography operations

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.