• Total site area: 100,000 sq ft,
  • Production – 43,500 sq ft
  • Laboratory – 3,000 sq ft
  • Warehouse – 18,000 sq ft

This facility has been custom designed and built to meet pharmaceutical requirements (PIC/S GMP Part 1) in terms of design, materials of construction, HVAC, and utilities that includes purified water, drains, electrical and lighting systems.

Production Area

Simpor’s manufacturing facility is GMP compliant and has an exceptionally skilled workforce. The most modern and advanced manufacturing equipment are utilized throughout all stages of production. Simpor’s manufacturing area is classified Class 100,000 Cleanroom standard.

Material Storage and Warehousing

Adequate temperature controlled warehouse space has been made available to handle incoming raw and packaging material, in-process stocks as well as storage of finished products. Warehouse access is restricted to designated personnel, security cameras have been installed and the flow of materials follow corporate procedures throughout raw material sampling, quarantine, release, issuance to production and finished product storage.

Cleaning and Sanitation

Manufacturing and packaging areas and equipment are cleaned according to approved cleaning procedures. Concentration of cleaning agents and frequency of use are determined by applicable validation studies.