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The Production buildings are sealed in such a way that air enters and leaves through opening provided. All such openings are protected by devices like Filter / Air curtains / Air locks.

TABLET, CAPSULE, LIQUID ORALS, POWDER, LOTION & NASAL BLOCKS
  • Tablet, capsule & ointment block is designed with 19 no of Air Handling Units using DX coil System, dedicated units of work in process and quarantine area.
  • Lotion Section designed with 3 no. of DX air handling units.
  • Powder section having 1 no of DX Air handling unit.
  • Injection sterile area provided with Airhandling units using chiller 60 kva.
  • All the process areas are designed to meet class 100000.(Not more than 25 C & NMT 60% RH)
  • All other areas meet the requirement of comfort air conditioning.
  • RH of NMT 60% is maintained by supplying direct exchange system.
  • All other process corridors are under positive pressure to reduce contamination.
Maintenance :
Tablet,Capsule, &Liquid Oral Section :
  • Separate staff for manufacturing and IPQC.
  • Layout to facilitate smooth movement of men and material.
  • Manufacturing activity is carried on ground floor & first floor and services are on the second floor.
  • Separate air-handling units for individual section, to prevent cross contamination with 24 hours cooling system for all WIP and quarantine area.
  • Full dust extraction system is incorporated.
  • Pressure gradient have been designed to ensure minimum contamination.
  • All service corridors are under negative pressure.
  • All critical area under negative pressure.
  • All operational area designed for the dust free transfer and there is no direct human, contact anywhere to cause contamination.
Beta Dry Injection(Sterile)
  • Separate staff for manufacturing and IPQC.
  • Layout to facilitate smooth movement of men and material.
  • Manufacturing activities is carried out on first floor and service area also at first floor.
  • Separate air-handling units for individual section to prevent cross contamination.
  • The manufacturing area design to meet class 100 (class B) for critical processes and other non critical process area class 10000 (class D) standard.
  • Pressure gradient have been designed to ensure minimum contamination.
  • All service corridors are under negative pressure.
  • All critical area under positive pressure.
  • All operational area designed for the dust free transfer and there is no direct human contact anywhere to cause contamination.
Quality Assurance informs Marketing /Distribution Dept. to identify the distribution of the product of the batch, which is to be recalled.
We manufacture finished Beta/Non Beta pharmaceutical formulations in the following categories & forms:

  • Dry Injection
  • Liquid, Orals Tablets
  • Capsules
  • Powders
  • Dry syrups
  • Ear/ Nasal drops
  • Ointments and creams
  • Lotions, Sachet
  • Bolus
  • Shampoo
  • Soap
More Information :
 

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