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.
This presentation provides an overview on the different types of water systems used in the Pharmaceutical Industry. Attendees will be provided a comprehensive overview of the different types waters systems, their validation, and handling of excursions. We will also 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?
Objectives of the Presentation:
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
Areas Covered in the Session :
Pharmaceutical water systems
Purification Process
Validation (IQ,OQ,PQ)
Daily monitoring requirements
Quality monitoring
Regulatory expectations
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