Any current Good Manufacturing Practice (cGMP) E.coli program must be based on a solid strain development strategy. This thought led to the development of Cytovance’s Keystone Expression System to provide a robust, high-yield E.coli strain to support cGMP manufacturing of a biologic.

The number and variety of protein therapeutics have increased dramatically in recent years. To satisfy therapeutic demand, these molecules must be produced at large scale in mammalian or bacterial cell hosts; but with the greater variety in protein therapeutic molecules

Process Characterization & Statistical Modeling — Transforming Data into Knowledge Throughout the Product Lifecycle, Upcoming Webinar Hosted by Xtalks. It’s no surprise that data plays a pivotal role in the biopharmaceutical industry.

Cytovance® Biologics announces the next webinar of its 2021 series: pDNA Manufacturing: An Optimized Platform Process. The webinar set for June 24, 2021 at 12pm EDT will feature a discussion on strain selection, plasmid optimization, media composition.

Cytovance Biologics, a leading biopharmaceutical contract development and manufacturing organization (CDMO) of mammalian, microbial and gene therapy biologics, announces its first webinar of the 2021 series: Regulatory Strategies for Gene Therapy Product Development.