Monitoring Product and Process Attributes in Biopharmaceutical Development and QC
This webinar was hosted live on October 19, 2016 by Genetic Engineering & Biotechnology News (GEN).
In this on-demand webinar, Waters Corporation's Jing Fang, Ph.D, and Robert Birdsall, Ph.D, discuss monitoring product and process attributes in biopharmaceutical development and quality control. You will learn:
- Several effective approaches for utilizing LC-MS-based workflows for monitoring multiple product and process attributes, and how selecting the correct one for your specific challenges can simplify deployment and improve the likelihood of success
- How a single, high-resolution LC-MS platform under the compliant-ready UNIFI® Scientific Information System can be utilized for product characterization in early development and then deployed to regulated late development and QC organizations for targeted monitoring of critical product and process attributes
- How the ACQUITY® QDa® Mass Detector operates, and how this technology can be deployed in compliant environments under Empower CDS for routine attribute monitoring of peptides, peptide variants, released N-glycan profiles, and more!
Watch the full on-demand webinar here: