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Facilities


Liquid Production | Demineralised Water Plant | Solid Dosage Manufacturing Unit | Quality Assurance | Services | Capacity | Strengths


 

In our pharmaceutical factory, based at Otta, we manufacture a number of high quality pharmaceutical products.

 

Liquid Production Facilities

Commissioned in 1999, this facility is equipped with manufacturing vessels, holding tanks, syrup making vessels of SS 316 international standard:

  • steam jacketed vessel - 2,000 litres
  • manufacturing vessels - 3,000 litres & 1,000 litres
  • storage tanks - 1 x 3,000 litres & 2 x 1,000 litres

The filling line consists of:

  • In-line bottle blower - an automatic container cleaning machine equipped with a build-in particle collection system. Output is approximately 75 bottles per minute. Container size range is up to 800 mm diameter and 200 mm high.
  • Filling station - Six adjustable filling nozzles make it possible to fill bottles of different volumes from 20 ml  - 200 ml. Output is approximately 60 bottles per minute.
  • R.O.P.P Capper CR90 - A single head roll-on-thread screw capping device which applies caps at up to 90 bottles per minute.
  • Self-Adhesive Labeller and Coding Machine - Fixes self-adhesive labels of varying sizes on line on to round bottles of 20 - 200 ml. A changeable coding device contains characters for printing batch numbers, manufacturing and expiry dates.

 

Demineralised Water Plant

The Pharma Plant has a central borehole of about 150ft (42m) deep providing potable water for the plant after a series of treatments.

A deionising plant provides processed water for pharmaceutical manufacturing that meets international standard.

Disinfection is by Ultrviolet light. Energy from UV lamp (source) to organisms (cellular material) which can result in death.

 

Solid Dosage Manufacturing Unit

Facility for the production of granules, tablets and caplets.

The facilities include:

  • mixers, granulators and sieving devices of SS 316 international standard.
  • two Glatt fluidized bed driers with electronic temperature control devices with other dust-proof components.
  • two Fette Perfecta 2000 tablet compression machines capable of producing tablets of varying sizes and shapes.
  • the packaging section is equipped with an Uhlmann stripping machine and 4 Uhlmann blistering machines.

 

Quality Assurance

The Quality Assurance Department is endowed with the latest in technology & equipment, allowing both chemical and microbiological analysis within the shortest time with a high degree of precision and accuracy.

Equipment includes:

  • Waters 712 WSP HPLC with Absorbance Detector.
  • Millennium High Performance Liquid Chomatography (HPLC) comprising of:
    • M600 Quartenary Gradient Solvent Delivery
    • M717 Plus Auto sampler
    • M996 Photodiode Array Detector
    • Millennium 2010 Chromatography Manager
    • Solvent Degasser Module 4 channels
    • Computer with printer
  • UNICAM 5625 UV/VIS Spectrophotometer with two Erweka DT6R Dissolution Rate Tester
  • Firlabo Stability chamber with digital control of R.H., Temperature and liightening.
  • Microbiology Laboratory recently installed and equipped with a Laminar flow Cabinet VBHL-6 class II Biohazard, Airborne Bacteria Sampler, Autoclaves, Incubators, Oven etc...

 

Services

  • Production of pharmaceuticals
  • Research and Development
  • Toll manufacturing
  • Toll Analysis
  • Consultancy services
  • Contract production trial
  • Regulatory Affairs Procedures & Documentation

 

Capacity

  • 750 million tablets per annum
  • 10 million bottles of liquid per annum

 

R & D Personnel (Pharmaceutical factory)

Key Personnel:

The pharmaceutical factories Research and Development section is  co-ordinated by Mr. S. O. Ajiboye, who has a B.Sc. in Biochemstry and an M.Sc. Pharm.Chem. and Mr. I. A. Oyegunju who holds a B.Pharm and M. pharm.

 

Strengths

  • Suitably located in Otta, with easy accessibility to Lagos and its nationwide distribution network
  • One of West Africa's leading production facilities
  • Good corporate relations with the pharmaceutical industry and regulatory bodies
  • Written Good Documentation Practices
  • Ready adaptability to GMP
  • Adequate warehousing facilities for own and contract materials and products, including ample cold storage
  • Modern and adequate communication system