Attendees will experience a thorough introduction to virus filtration as well as in-depth background and a mechanistic understanding about the principles of (parvo-) virus retention.

An interactive session will address the question of “how to design an efficient virus filtration process?” and a practical session will provide some hands-on experience with lab and production scale virus filter modules.

• R&D scientists
• Supervisors in manufacturing
• QA Manager (Regulatory Affairs, Pathogen Safety)

Upon completion of the course the participant will:

• have understood virus filtration principles
• have the ability to set-up and handle virus filtration processes
• have an overview of filter types and material
• have understood challenges of different matrices
• have gained hands-on experience with virus filters / process set-ups
• have understood principles/requirements of filter integrity testing
• have an overview of current guidelines and regulations

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