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

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.

Key Topics

• 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

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, 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