CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment
Why Should You Attend:
All non-waived laboratories must have a QC and QA plan that meets CLIA’s regulations. CLIA (Clinical Laboratory Improvement Amendments) has updated its requirements for QC and QA. CLIA has replaced the term Quality Assurance with the term Quality Assessment. The new guidelines regarding QA specifically stress measuring quality through all aspects of the testing process. This includes pre-analytical, analytical, and post-analytical parts of the process as a whole. QA is now focused on measuring outcomes and developing actions based on findings. The Quality Control process has guidelines in place for all three levels of testing; Waived, Moderately Complex and High Complexity. QA must be assessed, not check listed. Without measurement of quality your lab is missing an important component of assure quality outcomes.
Attend this webinar to understand the differences and the proper methods to meet the guidelines. It is important to understand that measuring quality is essential to assessing quality. The measurement of processes and the outcomes is the only way to truly assess quality.
Areas Covered in the Seminar:
- Quality Assurance vs. Quality Assessment: Why the Change?
- The Three Phases of Testing.
- Quality Assessment Systems That Work.
- Quality Control: Principles and Practice.
- QC for Waived Testing: Is Minimum Enough?
- QC Formulas and Their Use.
- Why QC and QA are linked processes.
- Measurement indicators for QA.
