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Migrating from immunoassay to mass spectrometry is a challenging endeavor for laboratories aiming to update their equipment and expand their diagnostic portfolios. Caroline le Goff, a European specialist in laboratory medicine based in Liège, Belgium, will share her experience making this transition and detail the evaluation of a kit "ready to use" for steroid panel and validation of an in-house method . She will also discuss method comparison, results validation, and going live with the assay.
WHAT YOU WILL LEARN
Understand the difference between an in-house method and a ready to use method concerning the analytical validation and method development.
Understand what is needed when validating a new technology to an existing workflow.
- Evaluate the results obtained in comparison to literature.
Caroline Le Goff, EuSpLM
Clinical Biologist, Department of Clinical Chemistry
University of Liège, CHU Sart-Tilman