Controlled, Continuous Lyophilization: Faster Drug Product Development & Flexible Manufacturing

Freeze-drying has long been one of the more stubborn bottlenecks in sterile product development: cycle times measured in days, high material demands at early stages, and a difficult bridge to GMP manufacturing. Continuous lyophilization is beginning to change that picture in meaningful ways.

This webinar brings together Thermo Fisher Scientific and RheaVita to examine how controlled continuous lyophilization is being applied within a working development environment, where cycle times have been reduced from days to hours without compromising critical quality attributes. The session covers small-scale implementation with minimal material requirements, flexible formulation and process strategies, and how a continuous approach can support a coherent path from early development through commercial production, illustrated with real-world examples.

Watch the webinar below to see how the approach holds up in practice.