We aspire to become a leading and reliable world class service provider to Pharma industry around the globe in the fields of Formulation development, contract research, Training, Impurity standards synthesis, Impurity profiling, Analytical method development, validation and its transfer and Stability studies of APIs/Drug products received from our valued customers.
Our consultancy services including Dossier development for world-wide regulatory authorities shall serve as a bench mark for others.
We are committed to a culture of continual Improvment in our system, process, services and product.
Our aim is to provide to our customers high quality services and products to contribute to healthcare of the society. We shall achieve this objective through process management and improvement in our activities to cater to the requirements of the regulated markets.