Our manufacturing facility enhanced production capacities for Liquid, Dry Suspension, Tablets and Capsule Sections for various therapeutic categories. Our manufacturing facility is equipped with the latest technology including automated process control system, computerized HVAC system providing with a ready compliance to cGMP, GLP, GWP and ISO 9001:2008. This has led us to formalize transnational relationship. The manufacturing team is committed to produce highest quality products which can meet the needs of both doctors and patients. The team strives to manufacture products that are cost-effective through best utilization of their resources, reduced down-time and by extensively applying planned-preventive maintenance program with coordination of highly skilled professionals.

Our production facilities meet the regulatory requirements of cGMP and regulatory authorities. All the manufacturing activities are performed according to the approved procedures as required by cGMP and ISO 9001:2008 quality management system. In addition to the procedure of quality assurance department at every stage of production, in-process checks are also imposed, and the results of which are continuously monitored and recorded. Materials are procured from approved suppliers through documented procedures, and quarantined until tested and released for use by the Quality Control department. These materials are dispensed under strictly controlled conditions supervised by our Quality Assurance team.