Many laboratories are unsure about which QC practices are needed and what criteria to use to assess the acceptability of the performance of analytical materials, to meet not only their requirements, but also to meet the requirements of ISO/IEC 17025. During this webinar, we will discuss a practical QC approach for in-house prepared and/or commercially purchased media, test kits and reagents specifically applicable to microbiology laboratories.
Why You Should Attend:
- To understand intrinsic and extrinsic factors which can affect the performance of culture media, test kits, reagents and other analytical materials
- To identify Control Points (CP) and Critical Control Points (CCP) in media quality assessment
- To develop appropriate QC Practices and acceptability criteria to evaluate the performance of analytical materials for laboratory use
Areas Covered in the Session :
- Control Points
- Critical Control Points
- QC from purchase to disposal
- Performance Criteria
- Sterility
- Productivity
- Selectivity
Who Should Attend:
- Microbiological Bench Analysts
- QA Managers
- Laboratory Managers/Supervisors
- QC Practitioners
