2018 Biopharmaceutical Webinar Series

Introduction to a new automated, efficient and highly reproducible approach to peptide mapping and associated compliant LC and LC-MS software.

Peptide mapping is a routine technique in modern biopharmaceutical characterization, but the technique is anything but routine as it is laborious and prone to errors and poor reproducibility. In this webinar we shall introduce you to a new automated, efficient and highly reproducible approach to peptide mapping and associated compliant LC and LC-MS software.

Speaker:
Tom. D. Buchanan, European Pharma & Biopharma Applications Development Scientist, Thermo Fisher Scientific, UK

Hear about latest technologies for aggregate and charge variant analysis including separation instrument requirements, new column chemistries and buffer systems for direct MS analysis to gain deeper insights in a compliant manner.

This webinar will discuss the latest technologies for aggregate and charge variant analysis including separation instrument requirements, new column chemistries and buffer systems for direct mass spectrometry analysis to gain deeper insights in a compliant manner.

Speaker:
Ken Cook, European Bio-Separations Manager, Thermo Fisher Scientific, UK

This webinar will look at the approaches and workflows to be able to conduct multi-attribute methods within a fully compliant CDS software.

Currently the many characteristics of biopharmaceuticals are analyzed by a variety of techniques to build up a complete picture. Multi-attribute methods or MAM use mass spectrometry to perform many of these characterizations and this webinar will look at the approaches and workflows to be able to conduct such multi-attribute methods within a fully compliant CDS software.

Speaker:
Marc Guender, Applications Expert Biopharma, Thermo Fisher Scientific, Switzerland

This webinar shows examples for intact, subunit and peptide analysis for biotherapeutics and discusses advantages and disadvantages of all three.

Modern mass spectrometers offer the ability to run intact, subunit and peptide analysis of biotherapeutics. During the webinar we will show examples of all three approaches, methodologies and discuss the advantages and disadvantages of all three.

Speaker:
David Muñoz, Biopharma Sales Expert EMEA, Thermo Fisher Scientific, UK

Overview of the current and future challenges in biopharmaceutical characterization and the strategies being developed by NIBRT to analyze such large molecules.

Biopharmaceuticals such as monoclonal antibodies are complex and consequently the array of tools and techniques required to fully characterize them is extensive. This webinar offers and excellent overview of the current and future challenges in biopharmaceutical characterization and the strategies being developed by NIBRT to analyse such large molecules as well as how Thermo Scientific Chromeleon CDS software simplifies system administration and ensures regulatory compliance.

Speakers:
Rowan Moore, Sr. Manager, European Pharma & Biopharma Applications Centre, Thermo Fisher Scientific, UK
Jonathan Bones, Principal Investigator, NIBRT, Ireland

Overview on new technologies and applications from Thermo Fisher Scientific for biopharmaceutical characterization and pharmaceutical applications.

To conclude this webinar series, join this session to learn about the new technologies and applications recently introduced by Thermo Fisher Scientific for both biopharmaceutical characterization and pharmaceutical applications.

Speaker:
Tom. D. Buchanan, European Pharma & Biopharma Applications Development Scientist, Thermo Fisher Scientific, UK

In this webinar, learn about the newest addition in our comprehensive portfolio of products for bio separations. Here we will focus on the fundamental criteria around weak anion exchange method design and the advancements in resin chemistries throughout the years.

Speaker: 

Dr. Ken Cook, EU Bio-Separations Manager and Stacy Tremintin, Product Manager - Thermo Fisher Scientific

This webinar is hosted by LCGC.

View webinar recording