White Papers

In many stages of mAb development, cell culture samples must be screened for IgG titer.

Continuous wet granulation and drying have long been a hot topic in pharmaceutical research and development (R&D) and industry.

Downstream processing is responsible for up to 80 percent of the entire production costs of biotherapeutics.

The first antisense drugs were approved, and clinical trials using siRNA show promising developments.

Discover over twenty application notes on biopharmaceutical purification.

Choosing the right filler-binder can enhance the overall taste and mouthfeel of pharmaceutical and nutraceutical products.

Use of static and dynamic light scattering to characterize the stability of lysozyme in the presence and absence of arginine.

How spray formulations and devices interact to impact drug delivery performance

This study demonstrates how DSC can be a useful tool in stability screening of engineered proteins

This paper shows the degree to which the technique of NTA can be used for the characterization of nanobubbles and other ultrafine bubbles.