Various contract manufacturing services for tablets, Syrups, Sachet and Capules are rendered to leading domestic as well as International Customers. The services encompass the whole process, beginning with confidential discussions, followed by a detailed offer and agreement, and transformation from laboratory/ pilot stage developmental work to commercial scale manufacturing of the intended products.

New business often starts at lab or pilot scale. In this regards, we have an independent fully equipped dedicated formulation development lab at which various new formulations / generic combinations in desired dosage form are being manufactured at laboratory and pilot scale.

Team of technical experts & Professionals are working for the development new / improved / desired formulations as per the requirement of the domestic & international customers.

Quality Risk Management (QRM) is also implemented during development and lifecycle of finished formulations to mitigate risk to patients and convene cGMP requirement of safe product. Accelerated / Long Term / Real Time Stability Studies are conducted as per the requirements of International Conference on Harmonization (ICH) guidelines.

The company also supports its customers in developing the CTD and other necessary documents required for the drug regulatory authorities of the relevant countries.