"Understanding the requirements for revalidation of molecular microbiology testing instrumentation can be challenging for laboratory leaders. Regulatory agencies such as CAP and CLIA often require revalidation but provide minimal guidance on what additional testing is required prior to putting instruments back into clinical use. Further, practical and actionable guidance on when and how to revalidate testing instruments is largely unavailable.
This webinar will provide an overview of the CAP/CLIA check list items relevant to revalidation of molecular microbiology testing instruments. It will also address when and how revalidations of instruments should be performed. Finally, using a case-based approach, it will discuss general best practices associated with revalidation of laboratory instruments, including to what extent (e.g., sample types, sample size, etc.) testing is needed for commonly encountered scenarios."