Newsletter | September 22, 2022

09.22.22 -- A CTO's Journey Into Continuous Biomanufacturing
 
Featured Editorial
A CTO’s Journey Into Continuous Biomanufacturing
 
A conversation with Chris Hwang, CTO, Transcenta Holding Ltd.

At a recent Evaluating BioPharma virtual event, moderator John Bonham-Carter asked Chris Hwang, chief technology officer at Transcenta Holding Ltd., about Chris’s journey and experiences with continuous bioprocessing thus far in his career.
How The Right CDMO Partner Can Accelerate Biologics Development
 
By J. Koleng, Ph.D., R.Ph. et. al.

The manufacturing lag in developing innovative biological therapeutics has created a bottleneck, so the industry needs better streamlining. That's where establishing a strategic partnership with the right CDMO partner can help to accelerate your development and manufacturing timeline.
Industry Insights
Quality Matters: SEC Analysis For Antibody Aggregates
White Paper | By Jon Lundqvist, Cytiva

Size exclusion chromatography is the go-to analytical method for therapeutic protein drugs. This article describes the factors affecting the reproducibility of columns and how you can minimize column variation.
Three Reasons Integrated CDMO Models Are Best
Article | Pfizer CentreOne

Some of pharma’s top brands developed their own responses to the demand for strategic outsourcing, creating a distinct class of contract development and manufacturing services suppliers.
Viral Safety Of Biologics: What's Changing With The ICH Q5A Revision?
Webinar | MilliporeSigma (Product Characterization)

ICH Q5A is currently being revised to address recent scientific advancements. We'll discuss the expected changes and potential impact on viral safety strategies.
Tech Transfer In Sterile Injectables: 3 Phases Of Success
Webinar | Pfizer CentreOne

Explore the three phases of sterile injectable project tech transfer, including how to bridge information gaps and facilitate successful regulatory filing at this fundamental stage of drug development.
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