In this webinar, the steam sterilization mechanism will be described as it relates to bacterial cells and endospores. The process and key terminology are defined. Understanding these fundamentals is critical to develop a successful autoclave sterilization process.
Why Should You Attend:
Successful autoclave Performance Qualification starts with a fundamental understanding of steam sterilization microbiology.
The webinar will lay out parameters of the sterilization process on a basis for conducting autoclave performance qualification studies. There are specific expectations for steam sterilization that must be met, whether it is continuing maintenance of existing equipment or qualifying a new autoclave installation. The session will also provide regulatory references on use of air removal verification tools, chemical indicators and biological, along with definitions for sterility assurance level, accumulated lethality, temperature mapping and biological verification.
Common questions and hot topics in industry will be presented to demonstrate the practical application of understanding steam sterilization. These points exemplify how the knowledge allows for efficient troubleshooting of unexpected events and for improving processes in an autoclave. Our expert will discuss the practical application of steam sterilization, address common questions, and cover industry hot topics. This knowledge will help professionals in efficient troubleshooting of unexpected events and for improving processes in an autoclave.
Areas Covered in the Webinar:
•Steam sterilization on a microbial level
•Autoclave Performance Qualification expectations
•Regulatory and GMP requirements for steam sterilization
•Process verification tools for use in an autoclave
•Common questions, problems and cGMPs
Who Will Benefit:
•Quality Assurance Managers
•Sterility Assurance personnel
Palo Alto, California
EVENT DATE: Monday, January 09, 2017 to Monday, January 09, 2017
Webinar information Brought to you by Biotechnology Calendar, Inc
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