Applying GMPs in Stages of Development
March 13, 2018 - Pharmaceutical Technology
Efficient Cleaning-In-Place Methods for Protein-Based Antibody Af
March 1, 2018 - Cytiva
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Impurity Testing of Biologic Drug Products
March 1, 2018 - BioPharm International
Industry Adoption of Single-Use Systems Remains Low
March 1, 2018 - BioPharm International
Preclinical Evaluation of Product Related Impurities and Variants
February 15, 2018 - BioPharm International
Preclinical Evaluation of Product Related Impurities and Variants
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Tools and Solutions for Separation of Charged mAb Variants
February 15, 2018 - Cytiva
A biosimilar is an almost identical version of
Exotoxin Clearance from mAb Samples in a Two-Step Chromatography
February 15, 2018 - Cytiva
A heat-stable exotoxin can remain as a contaminant of a d
FDA Framework Spurs Advanced Therapies
February 15, 2018 - BioPharm International
Techniques for Improving Process Development for Exosome-Derived
February 13, 2018 - Process Development Forum
An interview with Aaron Noyes, Head of Downstream Processing at Codiak BioSciences
Process Development: What May Lie Ahead in 2018?
February 1, 2018 - Process Development Forum
2018 is shaping up to be an interesting year in the