Production Department is the heart and running streamline of any industry. All the controlling and aiding departments are eventually working to ensure smooth and productive processing of materials which is the main domain of this department.

At Himark Laboratories., Production department is under the direct supervision and control of an extremely dynamic leader and team builder who has an experience of over 2 years comprising of his working in some of the top notch multinational industries.

Our manufacturing facility boosts enhanced production capacities for General Tablet (Coated, Uncoated, Enteric Coated Sustained released and Delayed released) Tablets, Liquid (Oral) Medicines, Capsules, Dry powder, Ointment and cream Section for various therapeutic categories.

The manufacturing facility is equipped with the latest technology including automated and dedicated process control systems, computerized HVAC/dust control mechanism, computerized Building Management System (BMS) and, Process–Water and Waste–Water Management Systems providing with a ready compliance to cGMP, ISO 9001:2015 .Delegates from Europe and the US have visited and admired the quality standards maintained at Himark Laboratories’ production facilities. This has led us to formalize transnational relationships and enhance our strategic partnerships.


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 a highly skilled engineering team.

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 9001:2015 quality management system.

In addition to quality assurance department’s procedures at every stage of production, in-process checks are also imposed, the results of which are continuously monitored and recorded. Materials are procured from approved suppliers through documented procedures, are quarantined until tested and released for use by the manufacturing department. These materials are dispensed under strictly controlled conditions supervised by our Quality Assurance team.

Our team’s in-depth know-how and expertise right from rapid drug registrations to generate substantial sales in short span of time.