Description

Developing best-practice approaches for optimising formulation, enhancing homogeneity and improving your freeze-drying processes

Industry representatives from across the globe, in industry and academia, will help you to:

Understand the FDA`s standpoint with regards to freeze-drying
Optimise your formulation strategies and improve your lyophilized products
Solve the challenge of inhomogeneity in lyophilized therapeutics
Rectify the problem of scale-up and tech transfer between pilot scale and commercial production
Utilise PAT and QbD tools to greatly enhance the way you freeze-dry
Appreciate the importance of ice-nucleation temperature in the lyophilization process
Assess the merits of spectroscopic monitoring to optimise the freeze-drying you undertake
Learn where spray-freeze-drying can be applied as an alternative to lyophilization

Lyophilisation for Biologicals 2011

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