Book Online Tickets for Steam Sterilization Microbiology and Aut, Palo Alto.  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 st

Steam Sterilization Microbiology and Autoclave Performance Qualification

 

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  • Group-Max 10 Attendees-Location

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  • 1x Person - Unlimited viewing for 6 Months

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  • One CD-USB is for usage in one location only

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  • Live + Recorded Version

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  • Live + Training CD-USB

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About The Event

 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
  • Supervisors
  • Validation personnel
  • Sterility Assurance personnel

Who Will Benefit:

  • Quality Assurance Managers
  • Supervisors
  • Validation personnel
  • Sterility Assurance personnel

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

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