December 10 2021
On demand
Online
Webinar
In this webinar, Michael Surace will review the factors which determine how stringent a validation should be, including the assay, the platform, the signal of interest, the reference signal, the degree of precision/ dimensions/ depth required in the analysis, the application, the purpose, the context, and the criteria for success. The standard development workflow for a 6-plex panel will be dissected and described in detail. The critical components of the low plex validation, including development tasks, pressure tests, and the formal verification, will be redeployed in a manner appropriate for a 40 plex iterative mIF assay, including caveats, potential artifacts, and criteria for success.
Dec 10, 2021
Speaker
Michael Surace, PhD
Associate Director
AstraZeneca