CLIA Guidelines on Quality Control and Quality Assessment
June 7, 2012
Location
Online Webinar
2600 E. Bayshore Road
Palo Alto, California 94303
USA
Description
This Clinical Laboratory Improvement Amendments (CLIA) training will be valuable to CLIA regulated non-waived laboratories that run automated analyzers or semi-quantitative kit tests.
Why Should You Attend:
All non-waived laboratories must have a QC and QA plan that meets CLIAs’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.
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.
Who Will Benefit:
This webinar will be valuable to CLIA regulated non-waived laboratories that run automated analyzers or semi-quantitative kit tests.All automated non-waived systems fall under these regulations. Employees who would benefit include:
- Chemistry and special chemistry supervisors and techs.
- Hematology and coagulation supervisors and techs.
- Blood bank supervisors and techs.
- Microbiology (automated) supervisors and techs
- Medical Technologists (MT)
- Medical Laboratory Technicians (MLT)
- Laboratory Directors
- Multiple Clinical Competency Technicians (MCCT)
- Clinical Lab Scientists (CLS)
- Point of Care (POC) Coordinators
- Medical supply reps
- laboratory instrumentation specialist
Organized by
ComplianceOnline
2600 E. Bayshore Road
Palo Alto, California 94303
United States of America
More Information
Contact: Referral
Email: referral@complianceonline.com
Phone: +1-650-620-3915
Event's Website
