Overview:
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.
Why Should You Attend:
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.
Areas Covered in this Webinar:
Control Points (CP)
Critical Control Points (CCP)
Quality Control from purchase to disposal
Performance Criteria
Sterility
Productivity
Selectivity
Learning Objectives:
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
Who Will Benefit:
Microbiological Bench Analysts
QA Managers
Microbiology Laboratory Managers/Supervisors
QC Practitioners
For more information, please visit our website of contact us:
Email: support@complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Level:
Intermediate
Speaker Profile:
Michael has been an Environmental Microbiologist for more than 42 years. He is a Past President of the Ontario Food Protection Association (OFPA), the International Association for Food Protection (IAFP) and AOAC International. He serves as Chair for the AOAC Expert Review Committee for Microbiology, as a scientific reviewer in Microbiology for the AOAC OMA and the AOAC Research Institute, as a reviewer for Standard Method for the Examination of Water and Wastewater and as a chapter editor on QA for the Compendium of Methods in Microbiology. He is also a lead auditor/assessor in microbiology for the Canadian Association for Laboratory Accreditation (CALA) and is Vice-chair of the CALA Board of Directors.
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.
Why Should You Attend:
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.
Areas Covered in this Webinar:
Control Points (CP)
Critical Control Points (CCP)
Quality Control from purchase to disposal
Performance Criteria
Sterility
Productivity
Selectivity
Learning Objectives:
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
Who Will Benefit:
Microbiological Bench Analysts
QA Managers
Microbiology Laboratory Managers/Supervisors
QC Practitioners
For more information, please visit our website of contact us:
Email: support@complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Level:
Intermediate
Speaker Profile:
Michael has been an Environmental Microbiologist for more than 42 years. He is a Past President of the Ontario Food Protection Association (OFPA), the International Association for Food Protection (IAFP) and AOAC International. He serves as Chair for the AOAC Expert Review Committee for Microbiology, as a scientific reviewer in Microbiology for the AOAC OMA and the AOAC Research Institute, as a reviewer for Standard Method for the Examination of Water and Wastewater and as a chapter editor on QA for the Compendium of Methods in Microbiology. He is also a lead auditor/assessor in microbiology for the Canadian Association for Laboratory Accreditation (CALA) and is Vice-chair of the CALA Board of Directors.
