BioPharm International-11-01-2016

November 01, 2017

Reliable, high-quality products require innovative analytics and production.

November 01, 2017

Siegfried Schmitt, PhD, principal consultant, PAREXEL, discusses how to prepare for an inspection by a foreign regulatory agency.

November 01, 2017

This article demonstrates that a modified SDS–PAGE can be easily used as a tool for quantifying the degree of protein degradation.

November 01, 2016

New data analytics tools help solve complex problems in a biotherapeutic development process.

November 01, 2016

In addition to having the optimal cell line and process, it is crucial to have the optimal cell culture medium and feed to maximize performance potential.

November 01, 2016

Advances in technology are increasing the productivity and efficiency of commercial-scale chromatography bioprocesses.

November 01, 2016

To investigate the best culture conditions, the authors used response surface methodology via Box-Behnken design.

November 01, 2016

CMO executives are focusing on M&A activity, new business models, and fundraising limits.

November 01, 2016

The development of mAb formulations poses challenges at the manufacturing, stability, analytical, and administration levels.

November 01, 2016

Vendor selection and materials testing are complex enough, but in today’s volatile environment, risk mapping and monitoring are also crucial.

November 01, 2016

Interactions between biologic drug products and the components of prefilled syringes can cause protein aggregation, but there are alternative materials that can help mitigate this problem.

November 01, 2016

Click the title above to open the BioPharm International November 2016 issue in an interactive PDF format.