3rd Annual Aseptic Processing Summit
20-21

November 2019

Austria

Vienna

About

Vonlanthen Group is pleased to invite you to the 3rd Annual Aseptic Processing Summit scheduled on November 20-21, in Vienna, Austria. At this Summit, participants will be given the opportunity to gather for discussion and to network with peers involved in pharmaceutical manufacturing, aseptic fill and finish, quality control, engineering and container development. Key topics in aseptic processing will be discussed by some of the industry’s leading lights. This conference will give you a broad overview of current changes in the European regu...

Vonlanthen Group is pleased to invite you to the 3rd Annual Aseptic Processing Summit scheduled on November 20-21, in Vienna, Austria. At this Summit, participants will be given the opportunity to gather for discussion and to network with peers involved in pharmaceutical manufacturing, aseptic fill and finish, quality control, engineering and container development. Key topics in aseptic processing will be discussed by some of the industry’s leading lights. This conference will give you a broad overview of current changes in the European regulations, modern technical trends and innovations.

more info
Who Should Attend

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

  • Bioprocess Research & Development
  • Container Development
  • Drug Development
  • Fill & Finish
  • Formulation
  • Lyophilisation
  • Nanomaterials
  • Packaging & Labeling
  • Process Monitoring & Control
  • Product Innovation
  • QA/QC
  • Risk Management
  • Stability
  • Sterilisation
  • Validation
  • Biotechnology
  • CMC
  • Engineering
  • Freeze-Drying
  • Licensing
  • Medical Devices
  • Parenterals
  • Pharmaceutical Process & Technology
  • Process Analytics
  • Packaging
  • R&D
  • Regulatory Affairs
  • Standardisation Science
  • Vaccine/Antibody/Cell Manufacturing
Key Practical Learning Points of the Summit

Innovations in aseptic pharma manufacturing
What does Annex 1 hold for sterile manufacturing?
Implementation of quality risk management
Process simulation/media fill
How to achieve a robust and reproducible production system
ADC/HPAPI aseptic processing fill and finish
Sterility assurance
Rapid microbial methods
Container closure integrity testing
RABS and isolator containment technology

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Sponsors and Partners

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