At Formatech, lyophilization development begins with the identification of a product specific liquid matrix and its freeze-drying characteristics. Often times, the main barrier to stability is a reactive solvent like water. Effective sublimation of this solvent will yield a dry stable product that can:
- Facilitate global transport and storage
- Withstand adverse environmental challenge
- Enable drug sponsors to expeditiously move through clinical trials
Following lyophilization cycle development and optimization, the processes are transferred to either our GMP Aseptic Manufacturing facility or to a facility of your choice.
