An important aspect during the manufacturing of drugs is the filtration used at different stages of the production process. Such (bio)pharmaceutical filters require validation to ensure optimum performance of the filters and maintain quality and efficacy of the end product and patient safety. In this webinar we will explore the key requirements and guidelines for (sterile) filter validation along with sharing some tips on how to simplify this process.

• Types of filters and guidelines
• Key considerations on the validation of (sterilizing) filters
  (compatibility, bacterial retention, extractables and leachables)
• Integrity testing and PUPSIT
• Extractables and leachables: A risk-based approach

3M School of Purification

The 3M School of Purification is a program designed by a team of 3M technical experts, with the purpose of educating the industry on a range of important biopharmaceutical separation and purification topics through a series of interactive and engaging webinars in 2022.

To learn more about 3M School of Purification and to view all previous webinars on-demand, visit the newly launched webpage: www.3m.co.uk/schoolofpurification