Water System Validation in Pharmaceutical Industry

This webinar will discuss the FDA requirements for design, validation and monitoring of pharmaceutical water systems. There are many different types of pharmaceutical waters and each must be fit for its intended use. Pharma water must be controlled for impurities. Pharma water systems must be designed, validated and monitored to ensure that the water produced meets specifications around the clock. Learn common pitfalls with water system design and use and how to avoid them. Get your pharma water questions answered in this webinar.

Areas Covered in the Session :

• Types of Water Systems used in the Pharmaceutical Industry
• Regulations Guiding Pharmaceutical Water
• Current USP <1213> Pharmaceutical Water System
• How pharmaceutical grade water is produced
• Validating a newly commissioned Water System
• Water System Validation by Logic
• Establishing procedures for maintaining the water system during its lifecycle
• Post Validation Testing
• Pharmaceutical Water Failure
• Presenting the results to auditors

Who Should Attend:

• Quality Assurance Departments
• Quality System Auditors
• Manufacturing Departments
• Regulatory Affairs Departments
• Research and Development Departments
• Engineering Departments
• Compliance Departments
• Microbiology Analysts and Technicians
• Lab Personnel
• Logistics
• Consultants