In the changing world of single-use
Sterile filtration has been a cornerstone of bioprocessing for over 60 years and as the industry continues its change from stainless steel to single-use, filtration has also evolved, moving from cartridge to capsule format with several membrane types to choose from. This webinar aims to provide an overview of filtration in bioprocessing addressing key considerations when developing a biopharmaceutical manufacturing process.
During the webinar we will discuss why sterile filtration is used instead of other methods of sterilization in bioprocessing before examining what makes a good filter membrane and what validation is required during the membrane development process. This will lead into filter selection considerations for different bioprocess applications.
The webinar will then go on to discuss filter integrity testing. We will look at different options available and how they are linked to validation to ensure your filtration process has been successful. We will also consider trouble shooting steps when integrity testing does not go to plan.
Register today for this webinar to begin optimizing your biopharmaceutical filtration processes to guarantee the quality of your product while reducing costs.
Presented by
Paul Hymus,
Product Manager (Filtration)
Paul has been with Parker for over 25 years during which time he has held various technical and product development roles supporting the growth of the Parker filtration business. Before moving into his current role as product manager for the life sciences filtration product range, Paul was responsible for the development of Parker’s point of use infection control portfolio.
