|
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. |