Quality Control is one of the key departments in any Pharma company. Large number of people works in the QC department.

Our manufactures are Athens labs ltd, Cosmas Research Labs ltd, Gnosis Pharmaceuticals, Logos Pharma, Regent Ajanta Biotech. They all are ISO-9001-2008 certified company.

These company qualities will be checked in three different stages.

1.      Raw material analysis

        Once the raw material enters the factory premises and before going to the Stores department the Quality of the material will           be checked by QC department. If the quality is as per the guidelines then the QC department approves the raw material. This           is called Raw material analysis. The concerned QC chemist will perform the basic duties and the Group leader or Manager                 approves.

2.     In Process Sample analysis

        The In Process Analysis will be done while the Product (Chemical or Formulation) is being Prepared/Manufactured

3.     Finished Product analysis

        Finished Product analysis will be done after the Product/material is manufactured.

Quality Policy

1.      Satisfy:- Need & Expectation

2.      Ensure:- Employee Involvement

3.      Build:- Quality at each and every level

4.      Assure:- Commitment to Society

5.      Invest:- Continuous Improvement

The quality control (QC) laboratory plays a critical role in pharmaceutical production, for both in-process and finished product testing.

Labs are like super-clean manufacturing environments, where significant attention must be paid to both safety and compliance. Equipment is often highly sophisticated, extremely sensitive, and very expensive; proper operations and maintenance are essential to avoiding equipment breakdowns. Labs are internal suppliers to the pharmaceutical manufacturing process, but like many service operations, their processes and “products” – timely test results – are mostly intangible and invisible in comparison with those of manufactured goods.