Well-integrated tests at each phase of manufacturing maintain the quality of the product from API to finished formulation. The API, excipients and packaging materials undergo a series of 160 tests to ensure availability of the best ingredient.

The product has to pass through 32 stringent quality tests during manufacturing and also after the finished formulation is ready. Thus, each vial passes approximately 200 quality tests before it is packed and transported.

Our closed isolator systems prevent external contamination from the isolator’s interior, by accomplishing material transfer via aseptic connection to auxiliary equipment.

Closed systems remain sealed throughout operations. The bulk solution preparation, filtration of the drug, filling, and stoppering of the medicine are done in a fully automated positive-filling line isolator. We are one of the very few companies with barrier isolation technology, thus ensuring that the quality we deliver is best-in-class.