Pharmaceutical Lyophilisation Summit

This premier event provides the appropriate platform to discuss and network with peers involved in pharmaceutical manufacturing, R&D, quality control, engineering, and container development.

The summit will shed light on practical considerations for freeze-dried formulation development, process optimization, validation and control for lyophilised biologics and vaccines.

Key Practical Learning Points of the Summit:

  • Manufacturing: critical issues and solutions
  • Process optimisation, monitoring and control
  • Innovations in formulation development
  • Model-based process engineering
  • QbD and PAT approaches
  • Strategies for scale-up from R&D scale to full production level
  • Technological solutions
  • Standards and validation
  • Regulatory considerations

Who Should Attend:

Chief Executives, Directors, Vice Presidents, Department Heads, Leaders, Senior Managers, Scientists, Chemists, Engineers and Fellows specialising in:

  • Bioprocess
  • Characterization
  • Container development
  • CMC
  • Drug development
  • Engineering
  • Freeze-drying
  • Formulation
  • Lyophilisation
  • Nanomaterials
  • Parenterals
  • Packaging and labelling
  • Process technology and analytics
  • Process monitoring and control
  • Packaging
  • QA/QC
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