Build for stability. Built for performance.

As scientists, we're always trying to find new methods to enhance productivity and automation in order to promote laboratory excellence. An advanced chromatography data system (CDS) can play a pivotal role in achieving these objectives.

In this on-demand webinar, you'll have the chance to listen to experts who will discuss the impact their CDS has had on their laboratory operations. You'll learn how their selection of CDS has made their lives simpler by significantly reducing data processing time and simplifying their workflows. Discover how they keep every step of the process, from sample injection to final result reporting, controlled in a secure, centralized location.

Key learning objectives

  • Learn how to accelerate data processing, reporting and reviewing to work faster
  • Understand how to simplify your analytical workflows within your CDS to deliver ease of use
  • Learn how to take control of your data by securing it in one location

Who should attend

  • IT department managers
  • Laboratory managers
  • Laboratory users
  • Quality assurance professionals
  • CDS system administrators

About the presenters

Laércio Fernandes, Product Marketing Manager, Thermo Fisher Scientific

Laércio Fernandes
Product Marketing Manager, Thermo Fisher Scientific

Laércio Fernandes is the Product Marketing Manager for chromatography software within the CMD Software team at Thermo Fisher Scientific. With a background rooted in analytical chemistry, sales and support, he has over 15 years of experience in the analytical field and has worked in constant connection with the Thermo Scientific™ Chromeleon™ CDS and chromatography instrumentation with a focus on Ion Chromatography. His background in sales and support has enabled him to have a good overview and understanding of different processes and challenges that laboratories may face, which has allowed him to better support our customers in order to improve their workflows and productivity.

Kayleigh Arthur, Lead Validity and Compliance Scientist, Owlstone Medical Ltd.

Kayleigh Arthur
Lead Validity and Compliance Scientist, Owlstone Medical Ltd.

Kayleigh Arthur is a Lead Scientist in the Analytical Validity and Compliance Department at Owlstone Medical Ltd. Kayleigh is an analytical chemist and mass spectrometrist with over 9 years’ experience working with LC-MS, GC-MS and ion mobility spectrometry. Her current work is focused on the incorporation of the GC Orbitrap technology to investigate a variety of volatile organic compounds in Breath Biopsy research.

Brian Alliston, Director, B. Alliston Limited

Brian Alliston
Director, B. Alliston Limited

Brian Alliston is a Chromatography Data Systems (CDS), data integrity consultant and director of B. Alliston Limited. Helping organizations meet regulatory challenges and maximizing the potential of their CDS software. He has over 25 years’ experience in the pharmaceutical industry and has been a Thermo Fisher Scientific™ Chromeleon™ CDS user and administrator for over 10 years.

Register to view the free on-demand webinar

* Required field

CMD Wide-format style fixes
Style Sheet for Global Design System