Our Turbhe manufacturing facility has 7 production lines dedicated to independently develop processes both in Solution and in Solid Phase.
We have strong expertise in both Solution Phase and Solid Phase synthesis of peptides
Our cGMP manufacturing facility in Turbhe has been successfully inspected by US FDA, EU authorities, EDQM, MFDS (Korea) and WHO.
At our Turbhe facility, we have a dedicated production line for Clinical Trial projects
We have the possibility at our GMP facility to upscale purification in any of purification lines using 5 cm to 30 cm diameter DAC columns.
We have a strong 60-member QC team equipped with the latest requirements for the characterization of peptides LC/MSMS, HPLC, Amino Acid Analyser, SOR, Ultra analytical balances in humidity-controlled rooms among others.
We have proven experience in delivering products for clinical trials to global customers.
Custom synthesis for mg to kg for New Chemical Entity.
Development of synthetic route for scale up to Commercial quantities.
Impurity synthesis, isolation, purification and characterization
Documentation support from R & D to commercial supply.