Pharmaceutical Water Systems - Validation, Monitoring, and Analyzing Data Results
Duration : 60 Minutes
Carl Patterson, MS, SSGB, SSBB,
Carl Patterson is a seasoned Pharmaceutical Manufacturing, Aseptic Processing, and Quality Assurance professional who is based in San Diego, California. As soon as he discovered the importance of biotechnology in the area, he was inspired to enter the pharmaceutical manufacturing industry. However Read more
This webinar will provide an overview of water systems used for pharmaceutical manufacturing. We will cover validation, monitoring, and analyzing data results. What data collected means, how excursions should be handled, and what actions can be done if a problem does occur. What can be expected when the water system is audited by regulatory bodies or clients.
Course Objective:
• Understand the USP as it pertains to water systems
• Outline the testing requirements for EP and USP standards
• Describe how several types of Pharmaceutical Water is made
• Validation approach to a new water system
• How to set-up a monitoring plan for the water system
• What to do if contamination is present
Course Outline:
• Types of Water Systems used in the Pharmaceutical Industry
• How pharmaceutical grade water is produced
• Validating a newly commissioned Water System
• Establishing procedures for maintaining the water system during its lifecycle
• Quality Control Monitoring of the water system
• Trending and presenting the results to auditors
• Case studies
What You Get:
• Training Materials
• Live Q&A Session with our Expert
• Participation Certificate
• Access to Signup Community (Optional)
• Reward Points
Who Will Benefit:
• Quality Assurance
• Logistics
• Manufacturing
• Quality system auditors
• QA directors and managers
• Microbiology analysts and technicians
• Consultants
• Regulatory and Compliance Management
Please reach us at 1-888-844-8963 for any further assistance or if you wish to register
