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

Get your copy of the guide today!

Fill out the Form
to Download the Guide!

All Indicates required field