Managing Risk in Biomanufacturing
June 28, 2017 - Cytiva

We simply cannot avoid all risks and the sta

Hybrid Bioprocessing: A Q&A with Andrew Sinclair
June 28, 2017 - Process Development Forum

Process Development Forum speaks about hybrid bioprocessing with Andrew Sinclair, President and Founder of BioPharm Services

N-Glycan Analysis of Biotherapeutic Proteins
June 28, 2017 - BioPharm Intl.

This article summarizes the approaches, challenges, and future perspectives for the characterization of N-glycans in biopharmaceutical products.

Immediate, Flexible Capacity with Hydrated Buffers and Process Li


June 28, 2017 - BioPharm Intl.

Fluids used in bioprocessing are typically pre

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.

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

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.

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

Previous PageNext Page