This seminar 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.
By attending this webinar participants will understand:
- 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
What you'll learn?
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 of waters systems, their validation, and handling of excursions.
Who should attend?
Professionals from Pharmaceutical Manufacturing Industry including
- Quality Assurance
- Quality system auditors
- QA directors and managers
- Microbiology analysts and technicians
- Regulatory and Compliance Management
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, his avid interest in all things biology, microbiology, and biochemistry officially began when he served in the U.S. Army as a Preventative Medicine Specialist and a Licensed Vocational Nurse.
To date, Carl has now garnered over two decades’ worth of extensive hands-on expertise. Currently, he is the Chief Consultant of his very own consultant business called aseptic-process.net, where he specializes in the aseptic processing of pharmaceutical products in the pharmaceutical manufacturing sector. Recently, he is in the process of creating webinars so he can share pertinent information about pharmaceutical manufacturing from a microbiological perspective.
Furthermore, Carl holds various degrees and certifications, including an M.S. in Biomedical Quality Systems from San Diego State University, a B.S. in Microbiology from the University of Texas, and Specialized Certificates in QA/QC & Biotechnology from UCSD.