Pre-Formulation and Formulation Development of a Sound Bio Pharmaceutical Formulation that is cGMP Compliant 2012

  • 10 May 2012
  • Webinar

Description

Topics
  • Selecting acceptable formulation components
  • Pre-formulation assessment
  • Antioxidants, stabilizers, surfactants, bulking agents, complexing agents, cosolvents
  • Buffers and buffer capacity
  • Eutectic melting, glass transition, and collapse temperatures
  • Crystalline vs. amorphous vs. mixed systems
  • Filling and fill volume
  • Thermal characterization techniques
  • Excipient considerations
  • Biomolecule stabilization theory
  • Infrared analysis of proteins
Who should Attend

Attendees from companies involved in developing lyophilization and formulations cycles, or in lyophilization product manufacturing, including Development Scientists, Quality Control Scientists, Quality Assurance and Production Management

Past Events

Important

Please, check "Pre-Formulation and Formulation Development of a Sound Bio Pharmaceutical Formulation that is cGMP Compliant" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Pharma
Technology: Biotechnology

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