Our state-of-the-art infrastructure is defined in a manner that enables to experiment, test, process, and check the reliability of our pharmaceutical products. Our infrastructural unit is widely spread in the area of 3000 sq. mt. with the facility of easy transportation of ready goods to the final destination. It is also resourced with all the facilities that are required for the production of liquid orals. Classified in three storey construction, our well-maintained infrastructure supports us in the manufacturing of the Pharmaceutical Dosage and Formulations in compliance of cGMP norms.

The manufacturing facility is built to comply with the cGMP Guidelines of WHO, Schedule M etc facilitating Closed transfer of material from dispensing to final filling stage.A well established and effective Quality Assurance System is in place to comply with cGMP guidelines. Periodic environmental monitoring of viable and nonviable count in the critical and support areas is done and documented.

The infrastructure includes all internal partition work done with 80 mm PUFF sandwiched metallic panels. Dedicated HVAC systems with environment control at individual production steps and auxiliary areas. Complete water management system with loop, separate storage and supply management system for each categories of drugs. Services including compressed air, refrigeration, electricity generation, purified water plant, distillation plant, ETP plants and boiler for steam generation are provided in the engineering block.