The A to Z`s of Microbial Control, Monitoring, Validation and Troubleshooting of Pharmaceutical Water Systems for Bio-pharma, Medical Devices and Cosmetics Industries 2016 is dedicated to all aspects of water systems and how biofilm manages to thrive there.
The A to Z`s of Microbial Control, Monitoring, Validation and Troubleshooting of Pharmaceutical Water Systems for Bio-pharma, Medical Devices and Cosmetics Industries 2016 covers topics such as:
- Successful Sanitization Approaches for Trouble-Free Water Quality
- What Makes Water Systems Have Microbial Quality Problems
- Implementing Changes to a Validated System
- Water System Validation by Logic Instead of Tradition
- Understanding and Controlling Endotoxin
- Reducing Water Microbial Excursions & Improving Investigations
- Microbial Enumeration Issues with High Purity Water Systems
- Harmonizing vs Optimizing Water Microbial Testing for System Quality Control
- What USP Does and Doesn`t Say about PW, WFI, Pure Steam and Micro Issues
- Water System Investigation "How-To`s" and Example Case Studies
The A to Z`s of Microbial Control, Monitoring, Validation and Troubleshooting of Pharmaceutical Water Systems for Bio-pharma, Medical Devices and Cosmetics Industries 2016 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, repairs, 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
- Production Managers involved with water system use for manufacturing and cleaning
- Change Control personnel involved in water system changes and repairs
- Laboratory Managers and Supervisors responsible for lab water systems and other water sources