Steam Sterilization Microbiology and Autoclave Performance - 2017
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 and Presenter Information
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.
Expected Number of Attendees
100Relevant Government Agencies
FDA, Microbiology
Event Type
Webcast
This event has no exhibitor/sponsor opportunities
When
Wed, Jun 7, 2017, 10:00am - 11:00am
Cost
General Admission: | $150.00 |
Website
Click here to visit event website
Organizer
NetZealous - Compliance4All