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
Sterility Assurance personnel
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.
Compliance4All DBA NetZealous,
Email: [email protected]
Full Details & Registration Link: