Autoclave Steam Sterilization & Applied Microbiology

Event Information
Product Format
Live Webinar
Presenter(s)
Conference Date
Add to my calendar   Wed, May 23, 2018
Aired Time
1 pm ET | 12 pm CT | 11 am MT | 10 am PT
Length
60 minutes
Product Description

Steam Sterilization: The Microbiological Component For Compliance


Whether qualifying a new autoclave installation or continuing maintenance of existing equipment, you must meet specific expectations for steam sterilization. After all, the goal of a successful autoclave Performance Qualification (PQ) is not just that the machine meets operating standards but that it achieves sterility.

Are you seeking a better understanding of the microbiology behind steam sterilization validation? Do you know what type of sterilization is right for your process—and the effects various types can have on your product/processes? This understanding is critical for a successful autoclave PQ—and pharmaceutical and biology expert Danielle DeLucy can help you get it.

In this information-packed webinar, DeLucy will describe the steam sterilization mechanism as it relates to bacterial cells and endospores. She will define key terminology and answers common industry questions as she demonstrates a practical application of steam sterilization. DeLucy will also lay out sterilization process parameters as a basis for conducting autoclave PQ studies.

After attending this webinar, you’ll have a firm understanding of sterility assurance level, accumulated lethality, temperature mapping, and biological verification. Plus, you’ll be confident with the regulatory use of air removal verification tools, chemical indicators, and biological indicators. In short, you’ll be prepared to troubleshoot unexpected events and improve your autoclave processes.

Session Highlights

This program will outline:

  • Autoclave Performance Qualification (PQ) expectations
  • Regulatory and good manufacturing practice (GMP) requirements for steam sterilization
  • Validation tools for use in an autoclave
  • Common questions, problems, and current GMPs
  • Mathematical explanation of D values

Who Should Attend

  • Microbiologists
  • Manufacturing managers
  • Validation engineers

Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.

Order Below or Call 1-866-458-2965 Today

You can also order through:
Phone

1-866-458-2965

Fax

1-919-287-2643

About Our Speaker

Danielle DeLucy

Danielle DeLucy, MS, is owner of ASA Training and Consulting, LLC which provides Pharmaceutical and Biologics based companies with training and quality systems  assistance in order to meet Regulatory compliance. Prior to this role, Danielle has been in the industry for 15 years serving in numerous Quality Management Roles, such as the Director of Product Quality, the oversight of Sterility Assurance practices and provided QA oversight of numerous...   More Info
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