Manufacturing

The Production is done as per specification of Master Formula Card (MFC), Batch Manufacturing Record (BMR) & Batch Packing Records (BPR) are maintained. All equipments are operated & cleaned as per (SOP's.) Deviations are minimized by adherence to above mentioned standards. All Equipments used for the manufacture are as per Good Manufacturing Practice and revised schedule-M. All Non Sterile, Non ß Lactum & Non hormones formulations are currently made in our unit for Tablet, Sterile ß Lactum and Sterile Non ß Lactum formulations are currently made in this unit as Small Volume Parenteral. The construction for ß Lactum department on first floor. All Equipments used for the manufacture are as per Good Manufacturing Practice and revised schedule-M.

We have following capacity for per month production based on single shift working.
Adequate space as per GMP have been provided for the storage of raw & packing Materials, manufacturing, testing, in process controls etc. Adequate measures have been taken to assure the quality of the products such as process & utility validations, proper sanitation, proper maintenance of equipments. All activities are performed by trained-skilled personnel and supervised by Competent personnel. Necessary records of all these are maintained. Stability studies are carried out as per WHO guide lines. In the plant, GMP norms are followed. Measures are taken to prevent cross contamination.