Increase Efficiency in Experimentation with Design of Experiments
January 27, 2017 - Cytiva

The Tide Stays High
January 11, 2017 - BioPharm Intl.

Robust venture capital investment gives CDMOs and CROs a positive outlook for 2017.

By Jim Miller

Drug Quality Key to Innovation and Access
January 11, 2017 - PharmTech

FDA plans to advance initiatives for ensuring reliable production of drugs and biologics in 2017.

By Jill Wechsler

How to Optimize Protein Desalting
January 11, 2017 - Cytiva

Most protein purification workflows r

Single-Use Extractables and Leachables: Cytiva's Alignment with t


January 11, 2017 - Cytiva

Despite years of discussion and experience, E&L tes

Efficient purification of meningococcal polysaccharides in a two-


December 9, 2016 - Cytiva

This application note demonstrates the purification 

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

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