Learn to develop appropriate quality control practices to evaluate the acceptability of media and reagents for laboratory use.
The webinar will discuss QC best practices and procedures for verifying the suitability and performance characteristics of microbiological media and reagents.
Why Should You Attend:
Many laboratories are unsure about which QC practices are needed to assess media performance to meet not only their requirements, but also the requirements of ISO/IEC 17025: 2005.
This webinar will discuss a practical QC approach for in-house prepared and/or commercially purchased media and reagents specifically applicable to microbiology laboratories.
In this webinar, attendees will learn:
- To appreciate intrinsic and extrinsic factors which can affect the performance of culture media and reagents
- To identify Control Points (CP) and Critical Control Points (CCP) in media quality assessment
- To develop appropriate quality control practices for CCPs to evaluate the acceptability of media and reagents for laboratory use
Areas Covered in the Webinar:
- Control points
- Critical control points
- QC from purchase to disposal
Who Will Benefit:
- Microbiological bench analysts
- QA managers
- Laboratory managers/supervisors
- QC practitioners
Michael Brodsky has been an environmental microbiologist for more than 42 years. He has been the president of the Ontario Food Protection Association, The International Association for Food Protection (IAFP) and AOAC International. He serves as co-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 Methods 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 board of directors.
Note: Use coupon code < NB5SQH8N > and get 10% off on registration, Valid till Dec 31st 2015
Organizer : Compliance online
This webinar will provide a detailed understanding about calibration and qualification of laboratory equipments, development of a qualification master plan, allocation of equipments to qualification categories A, B, C, and the approach for qualifying existing systems.