Join us for two Learning Curve Webinars
- 30 Minutes
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The landscape for manufacture of sterile medicinal products is evolving. Sterilizing filtration requirements are changing to reflect more complex fomulations. Expectations from regulatory authorities related to the evaluation of potential impurities or leachables for polymeric components with drug contact is also on the rise. We will share our updates on how we are working with end users to support them through these challenges.
Sterilizing Filtration Validation Requirements
Validation Project Manager (Scientist II)
Elisabeth is a project manager within the European Validation team, supporting customers to document their Pall filter and single-use technology validation, to ensure their sterile manufacturing process will perform as intended in alignment with GMP requirements and industry guidelines.
The Pall Approach to Evaluation of Extractables and Leachables
Senior Manager (Analytical Chemistry Laboratory)
Westborough, MA, USA
Benben is a Senior Manager and is responsible for extractables and leachables services. Benben holds a PhD in Bioanalytical Chemistry from Stony Brook University.
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