As a lab manager or bench analyst, you know that poor quality control (QC) leads to compromised performance of culture media, test kits, reagents, and other analytics materials. What you need is a sound—and practical—solution for assessing the acceptability of analytical materials’ performance, not just to meet lab requirements, but also to comply with ISO/IEC 17025.
Gain that practical QC solution in this webinar presented by pharma industry expert Michael Brodsky. He will show you how to take a performance-focused approach to employing in-house-prepared or commercially-purchased analytical materials in microbiology lab settings. He will also explain both the intrinsic and extrinsic factors that can affect materials’ performance and show you how to identify control points (CP) and critical control points (CCP) in a media quality assessment.
After attending, you’ll be able to develop QC practices that effectively evaluate analytical materials’ performance. You’ll understand performance criteria and why they are important, the difference between quality control and quality assurance (QA), and the difference between a lot and a batch. Don’t get hung up applying ineffective QC standards—learn today how to move forward with confidence!
Join this webinar to answer these critical questions:
Who Should Attend
Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.
Michael Brodsky has been an Environmental Microbiologist for more than 44 years. He is a Past President of the Ontario Food Protection Association, the International Association for Food Protection 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 Official Methods of Analysis and the AOAC Research Institute. He is a reviewer for Standard...
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