Unifying Continuous Biomanufacturing Operations
June 14, 2017 - BioPharm Intl.
The success of a truly integrated continuous processing platform relies on the collaborative efforts of upstream and downstream specialists.
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Managing Residual Impurities During Downstream Processing
June 14, 2017 - BioPharm Intl.
Increased understanding of potential impurities has spurred efforts to standardize monitoring procedures.
By Cynthia A. Challener
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Tips for Protein Purification Method Editing
May 31, 2017 - Cytiva
Protein purification questions and answers from ÄKTA club web chat.
The Extreme Costs of a Bioburden Incident
May 18, 2017 - Cytiva
The cost of bioburden incidents can vastly outweigh the costs of preventing them.
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Protein Purification Questions and Answers from ÄKTA Club Web Ch
May 18, 2017 - Cytiva
Do you have recurring discussions in your lab that you need input
Fusion Proteins Pose Manufacturability Challenges
May 18, 2017 - BioPharm Intl.
The unique structures of fusion proteins lead to expression, heterogeneity, and stability issues.
By Cynthia A. Challener
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Sources of Bioburden You Might Have Missed
May 4, 2017 - Cytiva
A problem with traditional mAb manufact
Witnessing Major Growth in Next-Generation Antibodies
May 4, 2017 - BioPharm Intl.
Including next-gen antibodies in pharma pipelines is considered essential for future success.
By Cynthia A. Challener
Being Thorough When Transferring Technology
May 4, 2017 - BioPharm Intl.
Communication and taking the time to develop the process are key to successful transfer and scale up of biologics.
By Susan Haigney
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Improvements in Protein A Chromatography
May 4, 2017 - Process Development Forum
Process Development Forum speaks about Protein A chromatography with Glen Bolton, Scientific Director at Amgen. Bolton recently published a pap
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