Biosimilars to Drive Modern Manufacturing Approaches
December 9, 2016 - Pharm Tech
Reliable, high-quality products require innovative analytics and production.
By Jill Wechsler
Managing Risk in Raw Material Sourcing
December 9, 2016 - Pharm Tech
Vendor selection and materials testing are complex enough, but in today’s volatile environment, risk mapping and monitoring are also crucial.
…
Your Protein Purification Questions Discussed with Cytiva R&D Sci
December 8, 2016 - Cytiva
Within ÄKTA club, web chats are held. In the web chats, ÄKTA sys
Protein Characterization Using SEC: Three Webinar Takeaways
December 8, 2016 - Cytiva
The possibility to separate molecules by size under n
Automating Processes in Upstream Processing
December 8, 2016 - BioPharm Intl.
By Susan Haigney
BioPharm International spoke with Trevor Marshall, director of enterprise systems integration at
…
Efficient Purification of Pneumococcal Polysaccharides in a Chrom
November 28, 2016 - Cytiva
This application note demonstrates the purificatio
Efficient Purification of the Pertussis Antigens Toxin, Filamento
November 28, 2016 - Cytiva
This application note describes the purification of pertussis tox
Advancing Single-Use Technology Through Collaboration
November 11, 2016 - BioPharm Intl.
By working together to harmonize the highly variable steps within the biopharmaceutical manufacturing process, both end users and suppliers are making s
…
Validation of the production of influenza virus in ReadyToProcess
November 10, 2016 - Cytiva
This application note describes the validation of the single-u
A Platform Approach to Purification of Antibody Fragments
November 10, 2016 - Cytiva
Antibody fragments constitute a promising class of biopharmac