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Swiss operates a state of the art, sterile cGMP contract manufacturing Formulation-Fill-Finish facility, providing comprehensive pharmaceutical development and manufacturing services for sterile drugs and small molecule drug products. Our technical team has experience in developing immediate and controlled release sterile injectable formulations including clear solutions, suspensions, and emulsions.
Our Out licensing facility for Lyophilisation is also FDA approved and has been audited by authorities from worldwide. The full range of support is offered including QC testing, RA support, visual inspection, secondary packaging and temperature controlled storage.