Pall Biotech

Prepare for a Successful Validation of Liposome-Based Drugs

Download this guide to get recommendations for applying QbD principles for sterility assurance during aseptic processing.

You will learn about:

  • Timing of risk assessments 
  • Optimizing the sterile filtration process step
  • Validation test method development and optimization
  • Building safety factors into the manufacturing process

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