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The total production area is about 66000 squire feet, which is divided into 4 multistoried buildings. Penicillins , Cephalosporins, hormones and general products are manufactured in those buildings, which are separated physically from each other.
The following products are manufactured on site...
General products
Cephalosporins
  • Liquid sterile (terminally sterilized and aseptically filled ampoule)
  • Solid dosage (tablets and capsules)
  • Oral liquids
  • Topical cream and ointments
  • Vaginal preparations
  • Sterile powder (aseptically filled vials)
  • Solid dosage (tablets capsules and powder)
Hormones Penicillins
  • Oral gonadal hormones.
  • Sterile powder (aseptically filled vials)
  • Solid dosage (tablets capsules and powder)
 


Production Facilities

Manufacturing and packing operations are carried out according to validated methods through systematically qualified machines with full documentation at all stage of operations.


The production site follows the cGMP guideline for environmental requirements of the manufacturing and packing area, as well as comply with the EHS requirements..

We use USP grade purified water and water for injections. PW is generated by RO followed by EDI method. The water is distributed through highly sophisticated loops, made up of SS316 L, argon welded and boroschopically tested.


Highly sophisticated HVAC system are used to condition, monitor and supply clean air to the working zone according to the manufacturing zone concept, capture and control any dust, vapour, gas and fume generated, as well as treatment of recalculated and/or exhausted air. Temperature and moisture level are maintained at the desire level through this system.




Design of the room and air-conditioning system ensure :

  • Prevention of contamination of products
  • Protection of environments
  • Protection of people

There are different environmental zones maintained within the manufacturing area.

Planed, organized, ongoing raining programs take place based on written plan and are documented. Personnel at all level under go general cGMP and technical training appropriate to perform their job satisfactorily.

 
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