Facility
 

Environmental Controls :

To Prevent dustiness, air turbulence & possible cross contamination, the airflow in the manufacturing sections is directionally controlled through a systems of physical barriers, louvers, pressure gradients, air-locks & air-risers. The Airconditioning is maintained through a centralised chilled water systems, with separate air handling units for each manufacturing section, supplying dehumidified filtered air.

The Services :

For ease in material handling and safety of personnel 2.8 M wide passages are provided. Above the passages, service lofts have been constructed, which form the arteries of the plant supplying utilities i.e. steam, electricity, treated water, air-conditioning, forced draught & compressed air to various sections.

 

 

The Quality Control :

The Quality Control Department is adequately staffed for comprehensive analysis of all inputs (raw & packing materials), in-process control & finished goods testing, as well as validation of processes & equipment.

GOOD MANUFACTURING PRACTICES (G.M.P.)

Fail-safe, written down, standard operation procedures are followed in every task. Documents relating to manufacturing procedures are prepared for each batch under the direct suspervion of expert & experienced technical staff, which includes in-process controls & results obtained. The aim is to produce drugs of standard quality, potency, purity & efficacy for the Indian & Overseas market.

Microbiological testing of raw material and finished products. Physical & chemical analysis of raw materials, intermediates and finished products carried out by technically expert staff. Computerized Spectrophotometric determination of purity of raw materials, intermediates and finished products.

 

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