ON-DEMAND WEBINAR: Approach to HPAPI Suite Design in a Multi-Use Facility

As new drug targets naturally become more potent in the search for more effective therapeutics, there is a growing demand for capacity and capabilities in support. The development and manufacture of Highly Potent Active Pharmaceutical Ingredients (HPAPI) in a multi-use facility faces challenges of technical, procedural and a perception-based nature. Fundamentally, it all starts with the use of the right tool for the job.

This webinar will focus on the risk-based approach to facility and equipment design when faced with the unique challenges of being a Contract Development and Manufacturing Organization (CDMO):

  • User requirement specification development
  • Containment strategy risk assessment
  • Process hazard analysis
  • Flexible and expandable design
  • Validation strategy
  • Product changeover

Length: 35 minutes


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Adam Kujath
Global Senior Director, Manufacturing Science and Technology 

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