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.

It is an honour and privilege to invite you to participate in this Summit. We look forward to welcoming you at the Summit in Berlin this coming April!

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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