Steam Sterilization Microbiology and Autoclave Performance - 2017

  • Free
  • Published date: April 20, 2017
    • Fremont, California, United States

Overview:
Successful autoclave Performance Qualification starts with a fundamental understanding of steam sterilization microbiology.

Why should you Attend:
Sterilization process parameters will be laid out as a basis for conducting autoclave performance qualification studies. Whether qualifying a new autoclave installation orcontinuing maintenance of existing equipment, there are specific expectations for steam sterilization that must be met.

Areas Covered in the Session:
Autoclave Performance Qualification expectations
Regulatory and GMP requirements for steam sterilization
Validation tools for use in an autoclave
Common questions, problems and cGMPs

Who Will Benefit:
Quality Assurance Managers
Supervisors
Validation personnel
Sterility Assurance personnel

Speaker Profile:
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.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

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