2019 - Automating Clinical Diagnostic Assays

OVERVIEW
Laboratories need technological transactions all the time. From new ways to perform assays to outdated technologies, to new equipment pushes to the various needs of end-users, assays need to switch between technologies regularly. One needs to be able to easily and robustly transition assays from one technology to another. With this seminar, you will be able to fully understand how your assay is currently running and make note of what the new technology should be able to do. Then, you will learn how to slowly get the new technology up and running, validating the quality system, equipment and the assay itself. You will learn what you need to understand in the process of transitioning old samples onto the new system and deal with any potential issues.
LEARNING OBJECTIVES
What are the individual steps needed to perform the assay on the bench?
How will your assay adjust to your automation?
What are the pitfalls to look out for during the method transfer process?
How to scale up the assay validation of an automated system?
WHO WILL BENEFIT?
Senior management
Quality Assurance
Research and Development
Bench Scientist
SPEAKER
Todd Graham is a clinical laboratory scientist for a large hospital system in the New York Tri-State Area, as well as a scientific consultant for Fortune 500 biotechnology firms, healthcare systems throughout the world and R1 Research Level Universities. During his time as a clinical laboratory scientist in his current role, Todd has improved sample workflow and improved laboratory quality and sample turnaround time while expanding laboratory services to vulnerable health populations in the New York area.
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