Best practices in global flow cytometry quality control and harmonization

Harmonizing flow cytometry data and quality control across the globe.
This webinar will provide an overview of best practices for global quality control and harmonization of flow cytometers. The discussion will cover industry best practices for harmonizing flow cytometry data, the role of bench-side quality control testing within larger quality management structures, and the application of concepts like ‘total error allowable’ and ‘statistical process controls’ to real-time quality control monitoring of flow cytometry assay performance.

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What will you learn?Who may this interest?Speaker

What will you learn?

  • Industry best practices for harmonization of flow cytometry data.
  • Where bench-side quality control testing fits into larger quality management structures.
  • ‘Total error allowable’ and ‘statistical process controls’ as applied to real-time quality control monitoring of flow cytometry assay performance.

Who this may interest?

  • Flow cytometry specialists and lab technologists
  • Quality control and assurance professionals
  • Clinical researchers
  • Clinical operations

Speaker

Brendan Ffrench, PhD
Senior Manager, Laboratory Operations
ICON

Brendan has extensive expertise in flow cytometry (15+ years). At ICON Central Laboratories, he manages the flow cytometry team at the Dublin location, which is part of the globally harmonized network of ICON flow labs spanning Lenexa, New York, Dublin, Assen, Singapore and Beijing. Along with the Global Flow Cytometry Management team, Brendan is involved in innovating ICON’s flow operations quality systems, enhancing performance across CAP/CLIA/ISO:15189 environments, and championing data-driven improvements in flow cytometry assays to support clinical trials with cellular immunology read-outs.

This webinar was recorded on 5 March.

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