The aim of this course is to familiarize students to the methods to verify the quality of diagnostics kits in a clinical laboratory. Validation procedures, measuring total allowable error and steps to introduce new tests will be presented. Topics covered will include compliance with proficiency testing requirements (CAP, AABB, CBAHI and ISO), determination and validation of tests reference ranges, cut-off points and quantitative and qualitative methods evaluation.
Grad Scheme
Letter
Prerequisites
None