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Results For "prep"

68 results found

Managing Residual Impurities During Downstream Processing Blog Post

Increased understanding of potential impurities has spurred efforts to standardize monitoring procedures.

Impact of Manufacturing-Scale Freeze-Thaw Conditions on a mAb Solution Blog Post

The objective of this study was to assess the impact of manufacturing-scale, freeze-thaw conditions…

Improving Process-Scale Chromatography Blog Post

Chromatography is a crucial step in the purification of biopharmaceuticals and accounts for a…

Process Chromatography Selection for Downstream Processing Applications Blog Post

Industry experts discuss best practices for selecting a separation technology. Process chromatography…

An Integrated Approach to Ensure the Viral Safety of Biotherapeutics Blog Post

Use of continuous cell lines in the manufacture of biological therapeutic products, such as…

Continuous Processing for the Production of Biopharmaceuticals Blog Post

The biosimilars landscape is growing as market factors, such as pricing pressure, advanced…

A Risk-Based Genetic Characterization Strategy for Recombinant CHO Cell Lines Used for Clinical and Commercial Applications Blog Post

The Chinese hamster ovary (CHO) cell lines used for the production of recombinant therapeutic proteins…

Adherent Cell Culture in Biopharmaceutical Applications: The Cell-Detachment Challenge Blog Post

The necessity to detach cells from a culture substrate during cell harvesting remains one of the most…

Antibody Production in Microbial Hosts Blog Post

The biopharmaceutical industry is growing exponentially, driven by an ever-increasing demand for monoclonal antibodies (mAbs) and…

Going Small to Achieve Success on the Commercial Scale Blog Post

Biopharmaceutical manufacturing involves a series of complex unit operations linked together to…

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