BioProduction (Part of CPhi Europe)

Key Topics

• Bioanalytical Method Development, Validation, and Transfer
  • Global regulatory requirements for bioanalytical method development
  • Benchmark with industry leaders on method development, validation, and transfer
  • Increase the speed of your method development time
• Protein Characterisation
  • New protein characterisation technologies and strategies
  • Critical Quality Attributes and Post Translational Modifications and how to measure them
  • Methods for analysing novel biologic formats and biosimilars
• Formulation and Stability Testing for Biopharmaceuticals
  • Latest advances and techniques in predicting the stability of biologics
  • Challenges in biopharmaceutical formulation development
  • Alternative forced degradation methods for stability testing of biologics
• Bioassays
  • The use of sensitivity analysis to set acceptance criteria in the validation of biological assays
  • Strategies for automating bioassays to increase speed and lower costs
  • Strategies and expectations for ADA assays
• Automation of Analytical Tools
  • Managing and evaluating large amounts of data from automation of analysis
  • Strategies to implement automation into existing analytical workflows
  • Automation to support product quality and meet aggressive deadlines