Biofilm properties, resistances, susceptibilities and examples
The "real" story behind some common water system design and control myths
Water system microbial enumeration issues
Water system sanitization to control biofilm
Improving outcomes and reducing the frequency of excursion investigations
Water System Validation and Change Control
What USP actually says about all this
How to perform successful Water System excursion investigations
Who should Attend
Quality Assurance personnel responsible for water system deviation management and change control
Microbiology Laboratory supervisors and analysts responsible for water sampling and testing
Process and Utility Engineers responsible for water system maintenance, troubleshooting, and excursion mitigation
Regulatory and Compliance professionals responsible for FDA interactions
Validation personnel for water system qualification
Facility Engineers responsible for water system design or renovation
Past Events
The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems 2012 - 24-25 May 2012, Renaissance Newark Airport Hotel, Elizabeth, New Jersey, United States (26008)
Important
Please, check "The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems" official website for possible changes, before making any traveling arrangements
