The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems is a conference that covers topics such as:
- 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
The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems brings together:
- 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